Longevity biomarkers: applications and limitations

Version 1 · Version 2 (current) · Rebuttal letter

Bow T. Shrike¹, Gustav Nilsonne², Vincent Weisser¹, Rakhan Aimbetov^1,*

¹ VitaDAO
² Karolinska Institutet, Stockholm, Sweden

* To whom correspondence should be addressed; r.aimbetov@gmail.com

Abstract

One major barrier to longevity research is evaluating the impact of interventions that improve human health and longevity because they are complex processes that occur over long time scales. Instead, measurable phenotypic traits or proxies of longevity, termed longevity biomarkers, may be used to assess the effectiveness of longevity interventions, or prognosticate clinical outcomes. Longevity biomarkers are critical tools for predicting lifespan and susceptibility to age-related diseases, but there exists a dizzying array of options, with at times contradictory readouts. Strengths of longevity biomarkers include providing insight into an individual's biological age, as opposed to chronological age, which is pivotal in evaluating targeted interventions that address aging and age-related conditions. However, most longevity biomarkers also exhibit notable weaknesses, such as a lack of specificity and lack of standardization across different studies and applications. These limitations underscore the need for more research to enhance their accuracy and reliability in long-term longitudinal studies. In the present review, we discuss key features of popular clinical biomarkers used to predict morbidity and mortality associated with advanced age, identify existing bottlenecks, and integrate the field consensus on further directions for robust life- and healthspan estimation.

Keywords: aging, biomarker, longevity

Introduction

The longevity research community confronts significant obstacles in evaluating the impact of health and longevity interventions. Presently, the most precise and dependable method for gauging an individual's health and longevity is through direct, long-term observation, which is both expensive and time-intensive. An alternative approach involves using biomarkers (Moqri et al., 2023). Biomarkers are measurable phenotypic traits that correlate with specific biological functions or their dysfunctions: “a defined characteristic that is measured as an indicator of normal biological processes, pathogenic processes, or biological responses to an exposure or intervention, including therapeutic interventions” (FDA-NIH Biomarker Working Group, 2016). Biomarkers offer a means to assess the effects of interventions more rapidly and accurately, providing insights into the mechanisms of aging and disease without the need to wait for a human generation to pass.

Historically, biomarkers were used for diagnostics and prophylaxis of morbidity. Some individual biomarkers correlate with all-cause and cause-specific mortality and burden of disease (GBD 2019 Risk Factors Collaborators, 2020). However, biomarkers in longevity research are limited due to inherent methodological constraints imposed by the aging process. For example, any biomarker exists and changes in several dimensions:

Temporal. Some biomarkers are useful on short timescales (less than one day), while others are useful across decades.
Tissue-, organ-, organ system-specific. Some biomarkers reflect changes in one organ system or one tissue instead of measuring organismal aging as a whole.
Pathophysiological. Some biomarkers measure pathology prevalent in old age instead of measuring aging in the absence of pathology.
Demographic. The predictive utility of a biomarker can vary by sex due to differences in physiology, an individual’s ethnic background, or environmental contributors.
Axiological. Not all biomarkers have the same value in terms of their predictive power. This underscores a crucial distinction between the total organismal phenotype, or the phenome, and the subset of clinically applicable traits, the clinome.
Epistemological. Although some biomarkers may robustly change with age, there is no clear idea of what these changes mean biologically.
Practical. Some biomarkers cannot be put to routine clinical use despite their theoretical significance due either to cost, ease of implementation, or ethics.

Although the field of longevity biomarker research has not yet matured, vital inroads toward an integrative framework for biomarker discovery and implementation have been made. To circumvent the outlined complexity, biomarker panels and combined scores in combination with ML/AI algorithms and dimensionality reduction techniques, such as principal component analysis (PCA), have been proposed to capture the aging biomarker dynamics in its entirety, extracting non-linear features of the aging phenotype from multimodal datasets (Pyrkov and Fedichev, 2019; Bafei and Shen, 2023). The concept of biological age and the development of associated aging clocks have significantly advanced our understanding of the biology of aging as a measurable quantitative trait, amenable to interventions (Ferrucci et al., 2020; Moqri et al., 2023).

Still, the longevity community is faced with systemic deficiencies. A recent survey of 395 professionals across various sectors of longevity identified major bottlenecks that hinder the translation of fundamental geroscience to the clinic (Florea et al., 2023). The absence of validated biomarkers was the primary barrier to progressing geroprotective interventions into clinical trials (tied with overall insufficient funding) (Florea et al., 2023). Most peer-reviewed studies on longevity biomarkers are small and exploratory, and most proposed biomarkers have never been tested in a replication study. The survey’s authors duly note that “to accelerate progress across the field, it may be more effective for investigators working on biomarkers to focus on the clinical validation of existing biomarkers rather than the development of new biomarkers” (Florea et al., 2023).

The same survey pinpointed the most impactful solutions to the identified bottlenecks (Florea et al., 2023). Across all participants, the availability of large-scale public datasets was mentioned most frequently (Florea et al., 2023). Consequently, the field needs consortia to come together and pool data in order to obtain large cohorts with sufficiently long follow-up times. Further, putative biomarkers need to be tested in combination so that the incremental value of one over another can be estimated.

The conceptual framework for biomarker discovery adopted by the American Federation for Aging Research is instrumental in the identification of useful candidates, setting three essential criteria for biomarker selection (Baker and Sprott, 1988; Butler et al., 2004; Sprott, 2010). First, a candidate biomarker should predict the outcome of a wide range of age-sensitive tests in multiple physiological and behavioral facets of aging better than chronological age. Second, it should predict remaining longevity at an age when 90% of the population is still alive, and account for most of the specific illnesses that afflict the species under study. Third, its measurement should be minimally invasive and not alter life expectancy or the outcome of subsequent tests of other age-sensitive tests (adapted from (Baker and Sprott, 1988; Butler et al., 2004; Sprott, 2010)).

Alongside the paramount importance of developing reliable biomarkers for longevity research, challenges hinder their implementation. One major challenge is the difficulty in comparing results across different studies. Variations in measurement protocols and biomarker value ranges can impede the comparison of individual results and the formulation of broad conclusions. A second challenge is that the response to interventions measured by biomarkers can vary greatly between individuals, complicating the task of identifying and quantifying intervention impacts. Finally, the lack of standardized protocols for validating biomarker results further complicates cross-study comparisons. This underscores the urgent need for both reliable biomarkers and standardized validation protocols to accurately evaluate the effects of interventions on health and longevity.

The core list of published research on the selected biomarkers used in this review was assembled by querying the Web of Science citation database (www.webofscience.com) with the ((“biomarker name”) AND (longevity OR ag*ing)) query, followed by sorting the output by descending citation number. Highly cited research papers, presenting population-level study results, were manually curated and used to outline the general narrative. Complementary publications were retrieved from PubMed (pubmed.ncbi.nlm.nih.gov) on an ad hoc basis to provide context and additional information where necessary.

In the present review, we first discuss what features biomarkers that forecast morbidity and mortality, or prospective biomarkers, should possess (Califf, 2018). Next, we overview the current longevity biomarker landscape, focusing exclusively on research done in humans, assess the biomarkers’ applied utility for health- and lifespan prediction, and interrogate their potential limitations.

Features of useful longevity biomarkers

Not all biomarkers are created equal. Here, we consider “good” biomarkers to be those with the following characteristics: 1) Discriminative ability, 2) Strong predictive power, 3) Strong correlation with the biological function, 4) Ease of measurement in humans, and 5) Low cost to measure.

A discriminative ability means there is a sufficiently large difference, with minimal overlap, between the values of interest. Consider two different biomarkers that measure the same phenotype, X and Y, calculated for three n = 1000-sized samples from three distinct populations (e.g. current smokers, former smokers, and never smokers) (Fig 1A). The means of both biomarkers, X and Y, are the same—50, 70, and 125—for these respective populations. Depending on how the values spread around the mean, there is a small (X) or a large (Y) degree of overlap between the biomarker values in the three populations, despite their means being the same – e.g. see sample 1 vs. sample 2 or sample 2 vs. sample 3.

Figure 1. Good biomarkers have strong discriminative ability, correlate with biological function, and have strong predictive power. (A) In three different theoretical sampled populations (blue, orange, and green), with sample size n = 1000 each, the means of biomarker X (top) and Y (bottom) values are the same for each sample taken from the given population (50, 70, and 125, respectively); differences in the biomarker means between the samples are statistically significant for X and Y in each case (1 vs. 2, 2 vs. 3, and 1 vs. 3). The greater variation in Y (standard deviation (SD) = 25) as compared to X (SD = 5) makes the former less useful as a biomarker due to overlap between the sample values from different populations. (B) Biomarker Z values within the population follow a normal distribution and can be divided into tertiles according to the biomarker Z readout. (C) Calculation of the odds ratio (OR) and relative risk ratio (RR) for an outcome (Y = yes, N = no), e.g. for the highest vs. the lowest tertile from (B), using absolute numbers of persons either exposed or non-exposed to the given tertile biomarker value range. The data were simulated and visualized using Python in JupyterLab. Created with BioRender.com.

However, the differences between populations for biomarkers X and Y are statistically significant in each case, with p-values approaching 0 due to sample size. P-values estimate the likelihood that the samples are derived from the same population, i.e. any observed difference is due to the sampling chance alone. At p = 0.05, which is a common statistical significance cut-off used in biomedical research, there is a 5% probability that we would have gotten the observed difference, or a more extreme difference, had the values on average not been different between the groups. While statistical significance (or p-value) is necessary, it is insufficient for establishing the biomarker utility. By calculating the effect sizes using the pooled measures of variance for two samples, we can see that the differences in biomarker X values are tighter than those for biomarker Y, which makes X a better estimator of the phenotype. Dynamic range is one key aspect of discriminative ability. Along with the dynamic range, a second aspect of discriminative ability is the age range over which the biomarker is useful. Some biomarkers may only be useful in the >50 age range, or not work in children.

A strong predictive power means that knowing the levels of the biomarker will let one accurately predict the phenotype in question. This implies that the biomarker needs to be hard to manipulate without also altering the phenotype. For example, consider grip strength: if grip strength is used as a proxy for general sarcopenia, training only grip strength could improve the biomarker without affecting overall muscle mass or improving lifespan.

Most quantitative biomarkers exist as a continuous variable. For example, assume a biomarker Z follows a normal distribution in the population, ranging from 0 to 125 arbitrary units (Fig 1B). The strength of predicting a certain outcome, measured by biomarker Z, would be expressed in terms of relative outcome probabilities associated with defined biomarker values or ranges thereof – e.g. for persons in the 3rd tertile according to the biomarker value vs. persons in the 1st tertile. Terms such as relative risk ratio, odds ratio, and hazard ratio are different epidemiological measures of effect size (Fig 1C). As discussed above, a large effect size is preferable. Importantly, the effect sizes calculated for sampled populations are point estimates (not true values) of the population parameter studied. To account for variability and sampling bias, point estimates are expressed together with confidence intervals – e.g. the true population parameter value lies somewhere within the specified range with 95% confidence (the 95% confidence interval, 95% CI). If the CI for a risk ratio includes 1, there might not be any difference between biomarker values in the parent population despite the significant estimated effect size in the sample.

A strong correlation with biological function means the biomarker is a good indication of the biology of what it is measuring. This can be measured by its correlation to other biological markers and its sensitivity and specificity to that phenotype. For example, if you measured blood pressure, you would want to see how it correlates with other cardiovascular markers like total cholesterol or pulse wave velocity. You would also compare performance between different ways of measuring blood pressure (e.g. electronic vs. manual sphygmomanometer).

Another key feature of a “good” biomarker is that it is easy to measure. Ease of measurement means biomarker detection uses assays that are quantifiable, have minimal operator bias, and can be performed with minimal training. For example, drawing blood is easy, whereas spinal taps are less so.

Finally, the cost includes the dollar amount per test, cost/availability of any specialized equipment needed, time to perform, and time to analyze. If a blood test performs equally well with an MRI scan, the blood test is superior. While costs for new technologies generally decline overall with time, lower costs allow for wider implementation. Implementing tests on a larger scale enables standardization and common interpretation of the test.

A large number of biomarkers exist to assess physiological parameters, predict morbidity and mortality, and forecast the effectiveness of therapeutic interventions. Here, we evaluate the most widely implemented biomarkers and their combinations—classical and novel—in clinical practice and evaluate their utility for biogerontology research. Since age-targeted longitudinal studies need reliable biomarkers reflective of a pro-longevity phenotype, a critical analysis of present approaches to risk and health estimation and the framework for appraisal of their practicality are of utmost importance. We first consider biomarkers by broad categories—physiological, neurological, laboratory, genetic, and epigenetic—discussing them on their own merit, and then evaluate the usefulness of combinations of biomarkers and combined clinical scores for lifespan and/or disease prediction.

Longevity biomarker landscape

Physiological

Herein, physiological biomarkers refer to non-molecular measurements of human morphology, body composition, and physical function. Although physiological biomarkers do not directly measure basic molecular processes underlying aging (Xia et al., 2017), they may be suitable for routine clinical use due to their key strengths: minimal or non-invasive nature, low cost, low technological requirement, and ability to collect longitudinal measurements. For example, physiologic biomarkers like grip strength, VO2max, gait speed, 30-second chair stand test, body mass normalized to height (body mass index (BMI)) or the composite Fried’s frailty index (discussed below), are widely applied in medical practice (Table 1). Seemingly unsophisticated, some phenotypic biomarkers outperformed early versions of DNA methylation-based biological aging clocks (see Aging clocks) in assessing health status of the individual (Belsky et al., 2018), or performed on par with the complex blood-based aging clock, PhenoAge (Liu et al., 2018; Pyrkov et al., 2021).

Evaluating physiological parameters of vigor becomes more important during age-related deterioration. Total and regional body fat (adiposity), and lean muscle mass, when coupled with functional parameters, i.e. various means to measure physical performance, serve as robust predictors of morbidity and mortality.

Aging is associated with an increase in adiposity and a redistribution of body fat to the abdominal or visceral regions (Kuk et al., 2009). Excess body weight alone increased the risk of death within 26 years of follow-up by 1% for each extra pound (0.45 kg) in the 30-42 years-old cohort and by 2% between the ages of 50 and 62 years (Kopelman, 2000). Furthermore, in middle-aged men, even more important than overall obesity as an independent risk factor for coronary heart disease (CHD) is abdominal obesity (Lakka et al., 2002). Abdominal obesity comprises both the subcutaneous fat that can obscure the abdominal muscles, and visceral fat underneath the abdominals. While subcutaneous abdominal fat and visceral fat are both determinants of central obesity, they have different profiles in terms of predicting morbidity and mortality. Visceral adipose tissue is a unique pathogenic fat depot (Fox et al., 2007). Visceral fat is a significant predictor of mortality in men after adjustment for age, follow-up time, subcutaneous fat, and liver fat (Kuk et al., 2006). Moreover, visceral fat correlated with markers of inflammation and oxidative stress (Pou et al., 2007), underscoring the relationship between visceral adiposity and metabolic health risks (Goodpaster et al., 2003, 2005).

In clinical practice, body fat is often estimated using a formula that attempts to correct weight for height: the body mass index (BMI). The BMI assumes that most variation in weight for people with the same height is due to fat mass (Kopelman, 2000). BMI is a strong predictor of overall mortality above and below 22.5–25 kg/m² (Prospective Studies Collaboration et al., 2009; Flegal et al., 2013). The progressive excess mortality above this range is attributed to vascular disease and may be causal. For example, at 30–35 kg/m², median survival is reduced by 2–4 years, whereas at 40–45 kg/m², survival is reduced by 8–10 years, which is comparable with the effects of smoking (Prospective Studies Collaboration et al., 2009). Thus, BMI is a valuable, albeit crude, population-level estimate of overweight and overall obesity (Lakka et al., 2002).

Since BMI fails to distinguish between the weight of fat and muscles or body frame, waist-to-hip ratio (WHR) and waist circumference (WC) are used to gain additional information on the nature of obesity (Williams et al., 1997). On average, each 1 standard deviation (SD) increase in WHR (0.06), WC (9.8 cm), and BMI (3.5 kg/m2) increased the mortality risk by >20% (Lakka et al., 2002). WC is a significant predictor of type 2 diabetes and cardiovascular disease after control for BMI, providing a reasonable approximation of visceral fat in clinical settings (Janssen et al., 2002; Kuk et al., 2006). Both general and abdominal obesity throughout adulthood is associated with an increased risk of pre-frailty/frailty in later years (Uchai et al., 2023). Thus, physical measurements serve as a first screen for factors that may limit human longevity.

These physical measurements can be refined in a laboratory setting. There, body composition can be measured using bioelectrical impedance analysis (BIA) (Kyle et al., 2004). This analysis assumes that the fat-free mass, which includes visceral organs, contains most of the water and conducting electrolytes in the body (Sergi et al., 2017). Using conversion formulas, BIA allows for the estimation of total body fat, total skeletal muscle mass, and muscle mass in the extremities, termed appendicular skeletal muscle mass (Sergi et al., 2017). Although these measurements require a lab, they can provide information on both body fat and muscle mass.

Loss of muscle mass is another factor associated with mortality, termed sarcopenia. Sarcopenia is defined as the “age-related loss of skeletal muscle mass plus loss of muscle strength and/or reduced physical performance” (Chen et al., 2020). It is associated with increased likelihood of adverse outcomes including falls, fractures, physical disability, and mortality (Cruz-Jentoft et al., 2019; Cruz-Jentoft and Sayer, 2019). While loss of muscle mass is one measure of adverse outcomes, recent diagnostic guidelines suggest that loss of muscle strength (dynapenia) is superior to loss of muscle mass (sarcopenia) for predicting adverse outcomes (Cruz-Jentoft et al., 2019). Notably, both men and women lose strength at a higher rate than they lose muscle mass (Goodpaster et al., 2006). Additionally, the robust correlation between strength and mortality persisted independently of low muscle mass, indicating that muscle strength, as an indicator of muscle quality, holds greater significance than quantity when estimating mortality risk (Newman et al., 2006). Due to technological limits, defining sarcopenia using muscle quantity and quality remains problematic (Cruz-Jentoft et al., 2019). Thus, strength might serve as an inherent indicator of mid- and late-life vitality and endurance that correlates with longevity into old age (Rantanen et al., 2000).

Maximal voluntary strength is a measure of the functioning of both the neural and the muscular systems, and thus may be an indicator of a person’s overall vigor (Rantanen et al., 2000). Both sarcopenia and dynapenia are assessed by muscle strength evaluations. Popular evaluations include grip strength (Roberts et al., 2011; Bohannon, 2019), 5-times sit-to-stand test (Muñoz-Bermejo et al., 2021), and the 30-second chair stand test (Jones et al., 1999). Muscle strength evaluations may be coupled with assessment of muscle quantity and quality using BIA or MRI. Mobility performance is appraised by a functional test, like measurement of gait speed (Studenski et al., 2011; Guralnik et al., 2000) or the 6-minute walk test (Enright et al., 2003; Enright, 2003) (Table 1). Except for grip strength, the other tests are more useful for the elderly where loss of function and performance compared to earlier life is seen.

Grip strength, which moderately correlates with overall strength, serves as a reliable surrogate for arm and leg strength. In healthy populations, hand grip strength measured during mid-life predicts risk of mortality from all causes over a follow-up of 25 (Rantanen et al., 1999), 30 (Rantanen et al., 2000), and 40 years (Metter et al., 2002), independent of BMI. The protective effect of muscular strength was evident across a range of causes of mortality and socioeconomic contexts (Leong et al., 2015). However, variations in measuring grip strength, such as dynamometer choice and protocols, may introduce measurement error, and hinder study comparisons (Roberts et al., 2011). Its ease of use makes it advisable for routine hospital and community healthcare practice.

Performance measures are basic integrators of the health of older people (Studenski et al., 2003). The relationship between physical activity volume and health status shows a graded linear pattern, indicating that the most active individuals experience the lowest risk of health issues (Warburton et al., 2006). Cardiorespiratory fitness (CRF), or “the capacity of the cardiovascular (heart and blood vessels) and respiratory (lungs) systems to supply oxygen-rich blood to the working skeletal muscles and the capacity of the muscles to use oxygen to produce energy for movement”, is a predictor of mortality independent of other factors (Booth et al., 2012; Ross et al., 2016). Exercise capacity is a powerful predictor of mortality: every 1 metabolic equivalent (MET; resting metabolic rate of 3.5 ml O2 kg-1 min-1 (Jetté et al., 1990; Franklin et al., 2018)) increase in treadmill performance was associated with a 12–15% improvement in survival (Myers et al., 2002; Harber et al., 2017). Further, risk-adjusted all-cause mortality (median follow-up of 8.4 years) was inversely proportional to CRF and was lowest in elite performers (≥97.7th percentile according to peak METs in a treadmill test): e.g. elite vs. low performers (<25th percentile) adjusted HR was 0.20 (95% CI, 0.16-0.24; P < 0.001) (Mandsager et al., 2018). The increase in all-cause mortality associated with reduced CRF, e.g. low vs. elite adjusted HR of 5.04 (95% CI, 4.10-6.20; P < 0.001), was comparable to or greater than traditional clinical risk factors, such as coronary artery disease, smoking, or diabetes (Mandsager et al., 2018). To sum up, CRF 2 SDs above the mean for age and sex displays the greatest survival compared with all other performance groups, with no apparent upper limit (Mandsager et al., 2018). In a clinical setting, the gold standard to determine CRF is VO2max, or maximal oxygen uptake under peak exercise load measured by open-circuit spirometry (Hawkins et al., 2007).

Regular physical activity significantly contributes to both primary and secondary prevention of various chronic diseases (Warburton et al., 2006). Any amount of physical activity is beneficial with a longevity benefit at 3–5 times the recommended leisure-time physical activity minimum (Arem et al., 2015). In addition to lower physical capacity, the overall activity becomes less frequent and intense with age, and with progressive shortening of the activity bouts that can be tolerated without resting, indicative of functional decline (Schrack et al., 2019; Wanigatunga et al., 2019).

Cardiovascular stiffness increases with age (Glasser et al., 1997; Mitchell et al., 2004; Zieman et al., 2005). A sedentary lifestyle during healthy aging is linked to decreased left ventricular compliance and diminished diastolic performance, an effect potentially reversed by sustained endurance training (Arbab-Zadeh et al., 2004). Vascular compliance can be measured using pulse wave velocity. The slower the pulse wave velocity, the greater the vessel compliance. Pulse wave velocity increased from 1% in both sexes aged 50 years to 64% in men and 74% in women aged 70 years (Mitchell et al., 2007). Pulse wave velocity significantly predicts all-cause mortality (Laurent et al., 2001). When adjusted for age, sex, and standard risk factors, individuals in the highest (11.8 m/s) aortic pulse wave velocity group had a HR for a major cardiovascular event of 3.4 (95% CI, 1.4–8.3; P=0.008) compared to those in the lowest (7.8 m/s) aortic PWV group (Mitchell et al., 2010).

Another measure of cardiovascular function is blood pressure. High blood pressure, or hypertension, is a major modifiable risk factor globally, affecting 34% of men and 32% of women aged 30-79 (NCD Risk Factor Collaboration (NCD-RisC), 2021). In absolute numbers, the prevalence of people aged 30–79 years with hypertension doubled from 317 million men and 331 million women in 1990 to 652 million men and 626 million women in 2019 due to population growth and aging (NCD Risk Factor Collaboration (NCD-RisC), 2021).

Hypertension is a principal contributor to the development of cardiovascular disease, stroke, renal impairment, and is a risk factor for functional and cognitive decline, physical disability, and dementia (Buford, 2016; Fuchs and Whelton, 2020). In a meta-analysis of 61 prospective observational studies, encompassing ~1 million people, a 20 mm Hg lower usual (long-term average) systolic blood pressure or a 10 mm Hg lower usual diastolic blood pressure at baseline was associated with ≥2-fold reduction in age-specific HRs for death from stroke, ischemic heart disease, and other vascular causes in middle age in men and women; the association was less pronounced, albeit still positive, in older age (Lewington et al., 2002). This relationship was evident with no threshold down to at least 115/75 mm Hg (Lewington et al., 2002). Moreover, non-vascular mortality positively correlates with blood pressure – with each 20 mm Hg lower usual systolic blood pressure corresponding to an age-standardized HR of 0.88 (95% CI, 0.87-0.89) (Lewington et al., 2002). In a study assessing the effect of modifiable risk factors on myocardial infarction incidence, hypertension accounted for OR of 2.48 (99% CI, 2.30-2.68), adjusted for age, sex, and smoking, with population attributable risk of 23.4% (99% CI, 21.7-25.1) (Yusuf et al., 2004).

The last cardiovascular parameter, heart rate variability, has predictive power in short-term (~5 min) and long-term (24 h) formats with lower values associated with higher cardiovascular risk (Shaffer and Ginsberg, 2017). Heart rate variability (by all measures) decreases with aging, falling below the threshold associated with an increased risk of mortality at >65 years (Umetani et al., 1998). Additionally, the heart rate profile during exercise and recovery is a strong predictor of sudden death (Cole et al., 1999; Jouven et al., 2005).

Reduced physical ability and overall weakness can be summarized with the term frailty. A working definition of frailty is used clinically to predict adverse outcomes in the elderly: falls, hospitalizations, disability, and death (Fried et al., 2001). Frailty is defined as a “biologic syndrome of decreased reserve and resistance to stressors, resulting from cumulative declines across multiple physiologic systems, and causing vulnerability to adverse outcomes”. The scale of frailty is quantized as having none, one, or more components of the composite phenotype: unintentional weight loss, muscular weakness, poor endurance and energy, slowness, low physical activity level (Fried et al., 2001). Frail people are more vulnerable to the effects of potential stressors and deterioration than others of the same chronological age (Church et al., 2020). Overall, frailty predicts shortened life and healthspan.

Neurological

Along with frailty, the decline of neurological function is one major organism-level sign of aging (Peters, 2006). Neurological phenotypes are most apparent in the waning of cognitive ability and changes in brain anatomy (Oschwald et al., 2019). Measuring these parameters provides feedback on key aging targets, and gives a functional measure of aging. Aging is characterized by a decrease in almost every neurological function tested, including cognition, vision, strength, steadiness, reactions, speed, coordination, fatigue, gait, station, sensations, and tasks of daily living (Potvin et al., 1980). Collectively, cognitive tasks that involve planning, assessing, and executing goals are termed executive function. Executive function also declines with age (Aging Biomarker Consortium et al., 2023b).

According to the “common cause” hypothesis, reduction in both sensory and cognitive function is a manifestation of the aging brain, so both can be used to gauge underlying organ deterioration (Baltes and Lindenberger, 1997). Sensory acuity is linked to cognitive performance, and this link becomes more pronounced as a person gets older (Lindenberger and Baltes, 1994; Baltes and Lindenberger, 1997). Scoring in the lower third of a multisensory test of hearing, vision, olfaction, and touch is associated with a 2 times higher risk of dementia and faster cognitive decline in adults aged 70-79 (Brenowitz et al., 2020). Importantly, hearing loss alone independently associates with cognitive decline and incident cognitive impairment in the elderly: there is a 24% increased risk compared to individuals with normal hearing at baseline (Lin et al., 2013). Based on a cross-sectional study, a 25 dB reduction in hearing is equivalent to a 6.8-year age difference as measured by executive function tests (Lin et al., 2011). This suggests that both multisensory loss and cognitive decline provide indirect measures of aging.

Neuroanatomically, aging is marked by a reduction in total brain volume, ventricular enlargement, and sulcal widening (Blinkouskaya et al., 2021). This can be partly explained by the reduced brain perfusion due to cardiovascular stiffness (Reeve et al., 2024). In people with atherosclerosis, for example, there may be continuous small hypoxic events which cause loss of brain tissue (Chojdak-Łukasiewicz et al., 2021). Other factors may include dementia, Alzheimer's disease, and other non-vascular etiologies (Peters, 2006).

Total and regional brain volumes can be measured by magnetic resonance imaging (MRI) (Blinkouskaya et al., 2021) (Table 1). Hallmarks of brain aging include alterations in brain anatomy, like an increase in ventricular volume, decrease in temporal lobe volume, and hippocampal atrophy (especially in individuals >70 years) (Scahill et al., 2003). Volumetric MRI in three age groups (14-34, 35-54, >55 years) with 3.5 years of follow-up revealed differential age-related changes in certain brain regions: longitudinal data showed a significant reduction in hippocampal volume, white matter volume (WMV), and total brain volume in two senior cohorts, suggesting these regions are vulnerable to age effects (Liu et al., 2003). For WMV, the volume difference between scans was at 2% (Liu et al., 2003).

In healthy adults, longitudinal changes in brain volume are not uniform. Regional gray matter, represented by cortical structures and prefrontal cortex in particular, is susceptible to differential aging-related effects (Raz et al., 1997; Lemaitre et al., 2012; Farokhian et al., 2017). This highlights the vulnerability of the most recent neural evolutionary acquisitions, i.e. associative cortices, as opposed to more ancient sensory parts of the brain (Raz et al., 1997).

Notably, in addition to the reduction in WMV with age seen by structural MRI, remarkable alterations have been revealed using diffusion tensor imaging/diffusion MRI (Sullivan and Pfefferbaum, 2006). Parameters like fractional anisotropy (FA) and mean diffusivity (MD) reflect diffusion directionality of water molecules and, indirectly, white matter integrity (Sullivan and Pfefferbaum, 2006). A decrease in FA, or increase in MD, suggest microstructural abnormalities in the white matter axonal orientation and its myelination. Importantly, these changes are similar to those seen in neurodegenerative diseases and are associated with cognitive performance (Raghavan et al., 2021).

Since brain anatomies reflective of age-related changes can be captured by imaging techniques, analysis and interpretation of the results become the next challenges. Brain MRI scans are combined with machine learning (ML) to construct “brain age” clocks (More et al., 2023). Aging clocks estimate a person’s age based on one cohesive set of biomarkers (see Aging clocks). Here, the brain age clocks estimate a person’s age based on brain scans. The brain age is then compared to the person’s chronological age, to determine a “brain-predicted” age difference. If the brain age is greater than the chronological age, it suggests aging-related brain alterations and implies accelerated degeneration (Franke and Gaser, 2019).

A brain age model based on T1-weighted MRI scans predicts mortality (but not morbidity) in older individuals: having a higher brain-predicted age difference significantly associates with mortality before the age of 80; each extra year of brain-predicted age led to a 6.1% relative increase in the risk of death between age 72 and 80 (HR = 1.061; 95% CI, 1.031, 1.091; P<0.001) (Cole et al., 2018). Furthermore, lower fluid cognitive ability, weaker grip strength, worse lung function, and slower walking speed all strongly correlated with an older-appearing brain, as demonstrated by a higher brain-predicted age difference (Cole et al., 2018).

A brain age estimate based on convolutional neural networks accurately predicted the chronological age of healthy adults using either processed volumetric maps or raw T1-weighted MRI data: the lowest mean absolute error (MAE) of 4.16 years was achieved for a model trained on volumetric gray matter input (Pearson’s R = 0.96 for chronological vs. brain-predicted age) (Cole et al., 2017). For raw unprocessed data, MAE was 4.65; R = 0.94 (Cole et al., 2017). On average, this suggests the brain aging clock can predict to within 5 years of chronological age, especially in persons >65 years.

One limitation of this approach is differences between scanners at different facilities. While reliable in a test-retest setting, pre-processing appears to be required to achieve between-scanner reliability for the brain-predicted age be suitable for use in both longitudinal and multicenter research. Refinements to brain age estimates include the blend of structural and functional MRI data, which outperforms either modality alone, with a MAE of 4.29 years (Liem et al., 2017). The multimodal approach, like the majority of the other techniques the authors evaluated, revealed a considerably increased rate of brain aging in participants with objective cognitive impairment (Liem et al., 2017). This supports the hypothesis that brain age and cognitive decline are connected (Elliott et al., 2021).

Laboratory

Serum markers are one subset of biomarkers that can be identified using laboratory tests on biopsies or bodily fluids. These biomarkers are important indicators of the efficacy of pharmacological and lifestyle interventions. Bodily fluids provide accessible and readily measurable markers of health and risk that correlate with life- and healthspan, and are routinely tested for a range of parameters to evaluate organ function and overall health. Some of these parameters correlate with age and age-related comorbidities (Justice et al., 2018). The most important biomarkers for aging gauge biochemical markers of aging, glucose and lipid homeostasis, inflammation, purine catabolism, and kidney function (Table 1).

Serum markers can provide insight into the connections between the brain and other systems of the body and organ aging. For example, the hypothalamic-pituitary axis, exerting its neuroendocrine influence on all aspects of human physiology, including energy metabolism, circadian rhythm, and reproductive function, is linked to five of the nine classical hallmarks of aging (Kim and Choe, 2019). The preserved hypothalamic-pituitary-testicular axis in exceptional longevity has been reported (Aleksic et al., 2022). Further, total testosterone and free testosterone levels are inversely correlated with cognitive impairment in aged males, highlighting the neuroprotective importance of this particular sex hormone—as well as an intact hypothalamus-pituitary axis in general—for healthy aging (Holland et al., 2011). This suggests multiple serum markers can be used to read out neurologic function, along with other systemic functions.

Another example of using serum markers to read out neurology phenotypes is a proteomic approach to assemble a panel of neurology-related serum proteins. A panel of 90 neurology-related protein biomarkers linked plasma proteomics to cognitive function and brain structure (Harris et al., 2020). The study sought to test if any associations between the neurology-related plasma protein levels and general fluid cognitive ability could be accounted for by structural brain variables. Of the 90 proteins, 22 were associated with general fluid cognitive ability in later life; 10 were mediated by total brain volume (Harris et al., 2020). These findings offer a method for the high-throughput and affordable detection of plasma proteins that may aid in the identification of neurologic biological pathways. Thus, both traditional and novel serum markers correlate with neurological function and may be useful for predicting the rate of age-related loss of cognitive function.

Glucose homeostasis is one of the key biomarkers for aging (Chia et al., 2018). The most basic test for the body’s ability to utilize glucose is fasting blood glucose (FBG) level (Sarwar et al., 2010; Palliyaguru et al., 2021). The weakness of this test is that it captures only a snapshot of glucose level variability throughout the day and fails to account for “spikes” and “dips” in concentration as a result of food intake, physical activity, stress, etc. Glycated hemoglobin (HbA1c), on the other hand, reflects the average blood glucose concentration in the few months preceding the test (because red blood cells have a lifespan of around 120 days) and thus serves as an accurate estimator of the glycemic status (Bennett et al., 2007) and a robust predictor of mortality (Currie et al., 2010). However, to achieve and maintain optimal HbA1c, the control of postprandial glucose levels is more important than FBG (Woerle et al., 2007). Further, 2-hour post-challenge blood glucose (2h-BG) is a better predictor for all-cause and cardiovascular mortality than FBG (Borch-Johnsen et al., 2001). Although all aforementioned parameters correlate with markers of cardiovascular health (such as markers of risk for atherosclerosis), the magnitude of postprandial blood glucose swings, rather than the mean values of glucose concentration over time, has the strongest association (Temelkova-Kurktschiev et al., 2000). This finding suggests the primary importance of acute postprandial fluctuation measurements over FBG or HbA1c for longevity biomarker purposes (Monnier et al., 2006).

Better correlates of cardiovascular health and morbidity are blood lipid parameters such as total triglyceride and total cholesterol levels. Nonfasting triglyceride levels are positively associated with the incidence rates of myocardial infarction, ischemic heart disease, and death (Nordestgaard et al., 2007). Similarly, total cholesterol is one predictor of ischemic heart disease and vascular mortality (Prospective Studies Collaboration et al., 2007). Cholesterol can be subdivided based on the type of particle carrying it. The ratios of total cholesterol or low-density lipoprotein (LDL) cholesterol to high-density lipoprotein (HDL) cholesterol demonstrate that HDL cholesterol has a protective effect against ischemic heart disease mortality (Prospective Studies Collaboration et al., 2007). Lowering LDL levels using statins reduces the risk of major vascular events irrespective of age, sex, baseline LDL cholesterol, or previous vascular disease (Mihaylova et al., 2012). Importantly, the association of ischemic heart disease-related hazard ratios with total, non-HDL, and HDL cholesterol becomes less steep with age, meaning these readouts are impractical for risk prediction later in life. Modulating cholesterol levels at late stages of life has a less pronounced effect on mortality (Prospective Studies Collaboration et al., 2007). In addition, longitudinal studies report that total, LDL, and HDL cholesterol decrease with age at about 1% per year, starting at age 65, in both men and women (Ferrara et al., 1997). Thus, cholesterol biomarkers are more useful for predicting untimely demise, rather than increased total lifespan.

Other serum biomarkers report systemic inflammation, which impacts life and health span. For example, C-reactive protein (CRP) and interleukin (IL)-6 are used as predictors of myocardial infarction and cardiovascular death (Pai et al., 2004). CRP is a marker for systemic inflammation and metabolic syndrome (Ridker et al., 2003), and is superior to LDL cholesterol in predicting cardiovascular events (Ridker et al., 2002). Depending on the concentration range at which CRP levels are detected, regular and high-sensitivity formats of the test exist, tailored to measure acute and low-grade inflammation, respectively (Wolska and Remaley, 2022). CRP correlates positively with total cholesterol, triglycerides, serum uric acid, body mass index (BMI), and negatively with HDL (Frohlich et al., 2000). Further, after adjustment for lifestyle factors, the ratio of total to HDL cholesterol, postmenopausal hormone therapy, diabetes, hypertension, and covariates such as BMI and lipid levels, the final pooled risk ratio of developing non-fatal myocardial infarction or fatal cardiovascular disease for men and women was 1.68 in the group with high levels of CRP (≥3 mg/L), compared to the group with low levels (<1 mg/L) (95% CI, 1.18-2.38; P = 0.008) (Pai et al., 2004). In a longitudinal study with a 9-year follow-up, higher baseline IL-6 and steeper increases in IL-6 over time associated with elevated multimorbidity, suggesting that this biomarker may serve as an early warning sign of impending health decline (Fabbri et al., 2015). Both IL-6 and CRP correlate with lifespan. In men, each standard deviation increase in either biomarker was associated with a 12-15% decrease in survival time and ~1-year shorter lifespan (Wassel et al., 2010). In women, the 7% reduction in survival time and 1.35-year shorter lifespan was linked only to IL-6 and depended on their estrogen therapy status (Wassel et al., 2010). These results underscore the sexual dimorphism in life expectancy and associated pathomechanisms, reflected in the biomarker behavior and its prognostic utility.

While inflammatory serum markers may impact life expectancy, they may not predict cognitive decline. Initial studies found these markers might predict age-related neurodegeneration and cognitive dysfunction (as early as 25 years prior to the onset) (Schmidt et al., 2002; Weaver et al., 2002). However, later evidence challenged the applicability of serum inflammation markers to assess a person’s cognitive status. In one prospective study aimed at establishing the link between several serum inflammation markers and dementia, IL-6 showed marginal influence, while CRP did not (Engelhart et al., 2004). A different marker for inflammation—α1-antichymotrypsin (ACT)—associated with all types of dementia examined (Engelhart et al., 2004). This was supported by a second study including four inflammation markers and several cognitive tests (Dik et al., 2005). In that study, high ACT strongly associated with worse performance, while elevated CRP, IL-6, and low albumin did not (Dik et al., 2005). These results were independent of other factors tied to cognitive decline, including apolipoprotein E (ApoE) ε4 phenotype, vascular diseases, and diabetes mellitus (Dik et al., 2005). However, a fourth study revealed a moderate association of CRP and IL-6, but not ACT, with cognitive function and decline, that was more robust in ApoE ε4 allele carriers (Schram et al., 2007). Thus, while systemic inflammatory factors may predict lifespan, their ability to predict cognitive decline remains limited.

Another serum biomarker that positively correlates with age and cardiovascular risk is serum uric acid. Serum uric acid levels increase with age (Kuzuya et al., 2002) and significantly correlate with hypertension (Sundstrom et al., 2005) and cardiovascular events, such as myocardial infarction, ischemic stroke, and all-cause mortality (Bos et al., 2006; Chen et al., 2009). In men, serum uric acid rises at a rate of ~7 μmol/L per decade (Zitt et al., 2020). In women, the level remains relatively constant until the age of 50, then increases sharply by ~20 μmol/L per decade thereafter (Zitt et al., 2020). Serum uric acid levels also associate with markers of sarcopenia, with mixed results. In a cohort of people with high handgrip strength, the hazard ratio of all-cause mortality was linear with serum uric acid levels (Guo et al., 2021). In the low-strength cohort, the relationship curve was J-shaped with higher ratios on either extreme of the serum uric acid concentration range (Guo et al., 2021). In contrast, other investigators observed that serum uric acid levels are positively associated with skeletal muscle index, grip strength, and gait speed (Liu et al., 2022). The reported contrasting effects of serum uric acid on overall mortality risk and functional capacity characteristics confounds the use of this biomarker for lifespan prediction and the assessment of health status.

Oxidative stress accompanies the progression of age-related pathologies. Recently, urinary 8-oxo-7,8-dihydro-2′-deoxyguanosine (8-oxo-dGsn) and 8-oxo-7,8-dihydroguanosine (8-oxo-Gsn), products of DNA and RNA oxidation respectively, were proposed as aging biomarkers (Gan et al., 2012). When normalized by urine creatinine level, both metabolites were positively correlated with age (Gan et al., 2018). 8-oxo-Gsn was more linearly age-correlated than 8-oxo-dGsn and was ~2-fold more abundant, suggesting it is more useful for physiological age estimation (Gan et al., 2018). For instance, higher 8-oxo-Gsn was significantly linked to frailty (defined as satisfying three or more Fried’s frailty phenotype criteria) (Liang et al., 2020). Age, heart rate, systolic blood pressure, hemoglobin, and Na+ independently associated with frailty in the same study (Liang et al., 2020). Furthermore, increased urinary levels of 8-oxo-Gsn associated with poor physical performance (grip strength, walking speed, repeated chair stand test) and cognitive function (Montreal cognitive assessment 5-minute protocol (Nasreddine et al., 2005)) (Jiang et al., 2022). One weakness of using 8-oxo-Gsn is the need for liquid chromatography-tandem mass spectrometry (LC-MS/MS). This renders 8-oxo-Gsn unsuitable for fast, straightforward, and operator bias-free implementation in the clinic.

Another group of serum biomarkers measure kidney function. Impairment of renal function correlates with an increase in cardiovascular risk (Schiffrin et al., 2007). One commonly used quantitative measure of kidney filtering capacity is glomerular filtration rate (GFR). GFR is estimated by plugging the serum creatinine concentration into various equations (Stevens et al., 2006). Notably, as a person gets older, and GFR worsens, the hazard ratios for death from any cause, any cardiovascular event, and any hospitalization progressively increase (Go et al., 2004).

One challenge with GFR is the choice of equation used to estimate it. The equation of choice needs to account for factors such as age, sex, race, and lean muscle mass, all of which affect muscle creatinine production (Knight et al., 2004). In addition, serum creatinine levels positively associate with confounders like smoking status, hyperlipidemia, and hypertension after adjusting for creatinine clearance (Knight et al., 2004). Moreover, in humans over 75 years old, the decline in GFR does not lead to increases in serum creatinine because the diminished filtration rate is compensated by lower lean muscle and creatinine production. This precludes the use of GFR across all ages (Fastbom et al., 1996).

One alternative to GFR is measuring cystatin C. Cystatin C, produced by all nucleated cells, may be a superior marker for GFR estimation than creatinine (Dharnidharka et al., 2002). Cystatin C is a strong predictor of all-cause mortality and the cardiovascular composite (death from cardiovascular causes, myocardial infarction, stroke) (Shlipak et al., 2005). However, like creatinine, this protein marker is influenced by non-renal factors. Older age, male sex, greater weight, greater height, current cigarette smoking, and high CRP levels each independently and positively associate with serum cystatin C levels (Stevens et al., 2009). Furthermore, the equation combining both creatinine and cystatin C performed better at GFR estimation than either marker alone (Inker et al., 2012). Additional renal markers may give a better picture of kidney function.

Along with serum markers, kidney function can be measured with urine biomarkers. Excretion of albumin in urine—albuminuria—is a sign of renal disease that often precedes age-dependent changes in GFR (Klausen et al., 2004). Urinary albumin predicts cardiovascular morbidity and general mortality in diabetic and non-diabetic, hypertensive and non-hypertensive patient populations (Gerstein et al., 2001; Hillege et al., 2002). Microalbuminuria (urinary albumin/creatinine ratio 30-300 mg/g) increases the cardiovascular risk 2- to 4-fold (Arnlov et al., 2005). Interestingly, the risk was still evident in patients with albumin to creatinine ratio well below the cut-off for microalbuminuria, possibly evincing underlying low-grade inflammation and endothelial dysfunction (Gerstein et al., 2001).

There are also many other serum molecules and proteins that can be checked to reveal various aspects of health. However, many of these reveal poor health, rather than limitations to lifespan. Furthermore, the complexity of the aging phenotype is reflected in the fact that it is unlikely that any single metabolite or protein is sufficiently robust for appraisal of long-term health, disease susceptibility, and associated risk. Laboratory tests aimed at a single biomarker suffer from both intraday variability and responsiveness to confounding influences such as lifestyle (sedentary or not, smoking status, alcohol consumption, sleep patterns, etc.), diet, fluid intake, body composition, sex, and the effect of other metabolic factors. These make the conventional tests relatively good assessors of health and risk at any given point in time, but poor longitudinal predictors of lifespan. To increase the predictive power of blood plasma biomarkers, panels of biomarkers and combined scores are needed (Murata et al., 2024). These panels may also consider genetic or epigenetic information.

Another approach is to compare differences in serum biomarkers between offspring of long-lived individuals and controls. This approach suggests that FBG (Rozing et al., 2010a), fasting insulin (Rozing et al., 2010a), free triiodothyronine (Rozing et al., 2010b), adiponectin (Atzmon et al., 2008), total cholesterol-to-HDL cholesterol ratio (Terry et al., 2007), and lipoprotein particle size (Barzilai et al., 2003; Heijmans et al., 2006) are different for long-lived families. While promising, additional validation of these markers is needed.

In addition to serum markers, the cellular blood component can serve as a robust biomarker of physiological decline (Yadav et al., 2024). For example, red cell distribution width, derived by dividing the standard deviation of erythrocyte volume by the mean corpuscular volume and expressed in percentages, increases with age (Lippi et al., 2014) and can be used to predict morbidity and mortality in the general population (Patel et al., 2010). Furthermore, our picture of lifespan can be broadened by leukocyte differential tests: a significant positive association between neutrophil-to-lymphocyte ratio and overall mortality has been reported (Cataudella et al., 2017).

Genetic and epigenetic

While biomarkers may report on health, the greatest factor governing longevity is an individual’s genetics. For example, using twin studies, frailty and falls are estimated to be more heritable than breast cancer (Steves et al., 2012). Furthermore, twin studies suggest genetics have a stronger effect on age of death after 60 compared to prior to 60 (Steves et al., 2012; vB Hjelmborg et al., 2006). If lifestyle was more important than genetics, one would predict a survivorship bias against poor lifestyle in extreme old age. However, in one retrospective analysis of long-lived Ashkenazi Jews (living independently, age >95), no differences were observed in lifestyle between those living a long time and those who did not (Rajpathak et al., 2011). This suggests that genes and their regulation underlie longevity. Along with measuring the DNA sequences in the human genome, gene expression levels (mRNA), non-coding regulatory RNA profiles, and relative protein abundances all vary with time, so these may provide feedback on current aging processes. Epigenetic markers, or non-genetic modifications to DNA and access to DNA, such as DNA methylation and histone modification patterns, also impact longevity. Finally, non-human genetics may impact longevity due to the profusion of microbes living in the human gut and other organs—the microbiome (Fig 2; Table 1).

Figure 2. The hierarchical relationship connecting clinical phenotype to the expression and regulation of genetic information. The flow of information in a cell proceeds from DNA (genome) to RNA (transcriptome) to protein (proteome). The epigenome modifies the hosts’ genome, regulating gene expression without altering the DNA nucleotide sequence. Genes, expressed as coding and non-coding RNA by the genome, form the transcriptome. Translation of protein-coding mRNAs creates the proteome, which is also influenced by post-translational modifications (PTMs) of proteins. PTMs also regulate the epigenome via histone modification. The proteome can directly impact the organism’s overall phenotype (phenome), along with the metabolites produced in biochemical enzyme-catalyzed reactions. In addition, the metagenome, which includes the microbes living on and in an organism, feeds into the metabolome and phenome. Finally, the phenome underlies the clinome, which is the set of clinical traits used to predict and measure disease. Created with BioRender.com. The icons were downloaded from icons8.com.

Examining the microbiome, or the genomes of the associated microbes living in our gut, skin or elsewhere represents a new genetic approach to assessing phenotypes (Yatsunenko et al., 2012). One strength of this approach is that sampling is straightforward and non-invasive because fecal samples can be analyzed for the gut microbiome. However, sequencing remains costly and there is large heterogeneity between individuals, complicating interpretation. One approach to solving this challenge is to analyze the metabolites produced by the microbial community instead of the community itself (Zhou et al., 2021). Metabolite analysis could improve interpretation of results because it will tie in to human metabolism directly, and because it focuses on the functional aspects of the microbiome (Fig 2). How well they compete with other measurements remains to be seen. The large heterogeneity of microbiomes between humans limits their application at this stage. Thus, microbiome analyses are best interpreted as developing technologies.

Human genetic markers have many strengths in predicting longevity. One strength of genetic markers is that sequence variation can be determined at any stage of the individual’s life, so early predictions/interventions could be tailored to an individual’s genetic make-up. Genetic markers have a track record of success in predicting risk to diseases that limit lifespan, such as cardiovascular disease and cancer (Ashley et al., 2012). Mutations in some genes have been identified as a major risk factor for the development of certain pathologies, e.g. BRCA1 and BRCA2 in breast and ovarian cancer (Antoniou et al., 2003; Mavaddat et al., 2013), whereas for other genes the relationship is causal, e.g. LMNA in Hutchinson-Gilford progeria (Eriksson et al., 2003; De Sandre-Giovannoli et al., 2003). Sequencing analysis is straightforward, and multiple targets can be evaluated per run. Marker analysis can vary from checking one or more single genes (e.g. IGFIR (Suh et al., 2008), APOE (Liu et al., 2013; Reeve et al., 2024), FOXO3 (Willcox et al., 2008; Gellhaus et al., 2023), INK4A (Kim and Sharpless, 2006)) to more comprehensive analyses of genomic differences (Sebastiani et al., 2012; Zenin et al., 2019; Deelen et al., 2019; Lin et al., 2021; Ying et al., 2024a).

Limitations of these markers include challenges in fixing the underlying problem, potential contributions of assortative mating, logistics of measurements, and ethical challenges. While genetic predictors that mark specific diseases are known, and genetics are known to have an effect on mortality, there is not yet a list of genes that predict longevity. Compounding this challenge is that we lack the technology to fix poor genetics, limiting the current utility of knowing the genes. Also, one alternative explanation for the contribution of genetics to longevity is assortative mating, or selection bias. Many heritability estimates assume human mate selection is random. However, if this assumption is false, the heritability estimates would overestimate the contribution of genetics to any given trait, including longevity. It is possible the contribution may be ~20% overestimated (Border et al., 2022; Ruby et al., 2018). Including assortative mating models could improve the estimation of genetic contributions to longevity.

Compounding these problems are the logistic challenges of cost and interpretation of the results. Compared to a skin or chair test, analyzing genetic markers is more expensive and requires additional interpretation. The population-level variability with some of these markers may also limit their predictive value. The ethical concern is discrimination against those with poor genetics for care and insurance coverage. Consequently, legislation may prohibit insurers from using genetic markers in their analyses, which limits the commercial development of these biomarkers. From a research standpoint, this is less of an issue because genetic markers are a starting point instead of an endpoint. Researchers may dive deeper into the mechanism, or use the genetic biomarker to identify a subset of people who would benefit from an intervention. For example, small non-coding RNAs like microRNAs may be used to predict neurodegenerative disease (Sheinerman and Umansky, 2013; Roy et al., 2022), while long non-coding RNAs may be used to assess autophagic function (Chowdhury et al., 2022).

Some limitations of genetic markers can be overcome by epigenetic markers because epigenetic markers take into account environmental factors that may be interpreted as lifestyle. DNA methylation patterns (Moore et al., 2013), histone modifications (Bannister and Kouzarides, 2011), and telomere length (Blackburn et al., 2015) are three common epigenetic markers. These epigenetic markers, especially methylated DNA patterns, serve as the foundation for biological clocks—an attempt to quantify the extent of the aging process independently of time alive (Fig 3; see Aging clocks). Consequently, epigenetic markers also have a strong ability to predict age. However, similar logistic issues exist compared to genetic markers. Sampling remains more invasive, and cost is higher than desired. While the legal and ethical risks may be reduced, they are not completely eliminated.

Figure 3. Biological age vs. chronological age. Biological age is an estimate of a person’s position on a molecular-genetic, physiological, and/or functional scale in relation to analogous positions of persons of the same age. In case the estimated biological age does not match chronological age—as expressed by positive or negative age delta—biological age acceleration or deceleration has occurred. Estimation of biological status can be potentially confounded by lifestyle factors, socioeconomic background, as well as the presence, absence, or degree of comorbidities. Created with BioRender.com.

Aging clocks

Genetic, epigenetic, and environmental factors affect both a person’s susceptibility to disease and lifespan, which limits the use of chronological age (time alive since birth) alone as a biomarker of aging. Chronological age fails to reflect a person’s risk of morbidity and mortality on longer timeframes. This occurs because humans age at different rates, with individual biomarker profiles often markedly deviating from populational trends (Ahadi et al., 2020). Therefore, there is a need to estimate a “biological age” (Fig 3). Biological age is an attempt to normalize the vagaries of human aging, and enable comparison of how much life a person may have left to live.

The primary tools for estimating biological age are “aging clocks”. Aging clocks employ various tools and approaches, depending on clinical endpoints and model data (Jylhävä et al., 2017). Aging clocks use data ranging from genetic and molecular level information to organism level information, though epigenetic DNA methylations were the first set of data used (Hannum et al., 2013; Horvath, 2013). The covalent attachment of a methyl group to the C5 a cytosine base at a CpG dinucleotide site to form 5-methylcytosine (5mC) modulates gene transcription in a tissue- and cell type-specific manner (Moore et al., 2013). The degree of DNA methylation at certain sites can be assessed in blood cells and tissues using microarrays, pyrosequencing, and whole-genome bisulfite sequencing (Ferrucci et al., 2020). DNA methylation patterns at CpG dinucleotide sites throughout the genome correlate with chronological age, so the first aging clocks were constructed by applying machine learning approaches to DNA methylation array outputs (Hannum et al., 2013; Horvath, 2013). The human genome contains many potential CpG methylation sites that can be used to generate non-overlapping epigenetic aging clocks (Porter et al., 2021). Depending on which CpG sites are used, distinct clocks that could reflect different aspects of the biology of aging can be generated (Porter et al., 2021). However, methylation levels at most CpG sites change minimally with age. For example, the average change of CpG methylation between the ages <35 and >55 years is 3.2% (Horvath and Raj, 2018). There is no consensus on what physiological differences these methylation changes signify (Bell et al., 2019). However, these aging clocks provide insights into the biology of aging, highlighting both tissue-/cell type-specific and universal aspects of associated temporal deterioration.

The earliest epigenetic clocks relied on modification levels of a few cytosines (Bocklandt et al., 2011; Garagnani et al., 2012). The methylation clock research gained traction after the introduction of elastic net procedure, which used more cytosines to increase predictive accuracy. The first two epigenetic aging clocks to utilize the elastic net were the Hannum clock and the Horvath clock. The Hannum clock measures 71 CpG sites from blood, and achieves a correlation of 0.96 between chronological age and predicted age with a 3.9-year mean error (Hannum et al., 2013). The Horvath clock used 353 methylation sites from multiple tissues, and had a similar correlation (0.96) to biological age, and error (3.6 years) (Horvath, 2013). Over the next 10 years, epigenetic aging clocks and their iterations based on cross-sectional data correlate with multimorbidity and mortality in diverse populations (Marioni et al., 2015; Chen et al., 2016; Zhang et al., 2017), and reflect the influence of environmental factors (Quach et al., 2017). Large longitudinal studies confirmed the utility of epigenetic marks in quantifying personal aging trajectories and risk prediction (Li et al., 2020; Belsky et al., 2022). Comparing results from these clocks to chronological age provides a measure of “accelerated aging”, where a large difference between a person’s biological and chronological ages is linked to higher risk and a faster onset of age-related morbidity.

Second generation epigenetic clocks improved on first generation clocks by incorporating physiological data into training sets. These clocks produced solutions tailored for morbidity/mortality risk estimation at the expense of chronological age prediction accuracy (Fig 4). For example, the aging clock PhenoAge uses methylation surrogates (epigenetic representations) of nine blood biomarkers plus chronological age to predict 10- and 20-year mortality, along with the aging outcomes of cancer, healthspan, physical function, and Alzheimer’s disease (Levine et al., 2018). These predictions were superior to the Hannum and Horvath clocks (Levine et al., 2018). A similar second generation aging clock, GrimAge, measures methylation surrogates of smoking pack-years, seven plasma proteins, chronological age, and sex; GrimAge outperforms first generation aging clocks in measuring time to death (Lu et al., 2019). Similarly, DunedinPACE aims to measure the rate of aging, and performs similarly to GrimAge (Belsky et al., 2022). This DNA methylation-based panel builds on data from a longitudinal cohort of individuals all born in 1972-1973, and improves on a panel of blood biomarkers (Belsky et al., 2022). This panel is used in the so-called “Rejuvenation Olympics”. Overall, DNA methylation clocks have improved since their initial debut.

Figure 4. Biomarkers and concepts used to measure longevity. Aging unfolds from the molecular/genetic level to the cellular level to the organismal level of organization, encompassing hierarchically more complex and extensive physiological networks. Individual and composite biomarkers, along with statistical and machine learning/artificial intelligence (AI) methods, can be used to measure the degree and speed of aging. BV, brain volume; CIM, carotid intima-media thickness; CNN, convolutional neural network; DNN, deep neural network; EEG, electroencephalogram; FI, frailty index; FRS, Framingham risk score; GAN, generative adversarial network; HRV, heart rate variability; L/GDA, linear/Gaussian discriminant analysis; MLR, multiple linear regression; NLR, neutrophil-to-lymphocyte ratio; NMF, non-negative matrix factorization; PCA, principal component analysis; PWV, pulse wave velocity; RCDW, red cell distribution width; SASP, senescence-associated secretory phenotype; SVM, support vector machine; t-SNE, t-distributed stochastic neighbor embedding; UMAP, uniform manifold approximation and projection. Created with BioRender.com. The icons were downloaded from icons8.com.

One reason for the improvement was moving away from training models to match chronological age. Minimization of predicted chronological age estimation error costs the model biologically relevant information like the ability to predict death (Zhang et al., 2019). More accurate models trained on chronological age data lose predictive power in terms of health or mortality risk (Pyrkov et al., 2018b). Instead, training clocks with phenotypical correlates of age-related decline, like changes in blood biochemistry (Levine, 2013; Putin et al., 2016; Mamoshina et al., 2019), daily activity pattern (Pyrkov et al., 2018a), and body constitution (Fermín-Martínez et al., 2023), yielded clocks that were more accurate predictors of morbidity and mortality. Integrating additional measures helped improve the accuracy of aging clocks.

Recent technological advances have provided more accurate information about gene function for assembling aging clocks. Developments in -omics beyond DNA sequencing and methylation arrays, such as transcriptomics and proteomics, allow the use of gene expression profiles for biological age estimates (Solovev et al., 2020; Rutledge et al., 2022). Since the cellular transcript pool and protein makeup represent the realization of genetic information, they provide a more direct and actionable understanding of pathways and networks involved in aging and pathology (Fig 2). For example, 1497 genes change expression levels with age (Peters et al., 2015), while 529 proteins change in abundance with age in human plasma (Johnson et al., 2020). This allows the construction of many different transcriptional and proteomic aging clocks. One such transcriptional aging clock had an average absolute difference between predicted and chronological age of 7.8 years (Peters et al., 2015). One example proteomic aging clock that measured 76 proteins in the blood proteome had an error of 5.7 years (R = 0.94) (Tanaka et al., 2018). Measuring the top eight proteins on this list sacrificed some accuracy, with a difference of 13.1 years (R = 0.92), while the top protein alone (GDF15) had a difference of 16.6 years (R = 0.82) (Tanaka et al., 2018). A second blood proteome model of 373 sex-independent proteins had good accuracy in predicting age in discovery, validation, and four independent test cohorts (R = 0.93–0.97) (Lehallier et al., 2019). The explosion of information enables the construction of more complex aging clocks.

Finally, measures of metabolites and microbes are also in development to measure aging. The identification and quantification of fluctuating metabolites as a function of biological age using mass spectrometry or NMR also measure age-associated risk (Panyard et al., 2022; Robinson and Lau, 2023). Attempts to measure aging via changes in the microbiome use “metagenomic aging clocks”. These clocks rely on the changes in intestinal microflora composition with age, health, diet, and exercise (Yatsunenko et al., 2012; Conlon and Bird, 2014). Distinct adult and elderly microbiome taxonomic profiles exist, with transitions around both 20 and 70 years old (Odamaki et al., 2016). A metagenomic aging clock built using a deep neural network trained on >4000 metagenomic profiles from healthy individuals aged 18-90 had a MAE of 5.91 years (Galkin et al., 2020b). Curiously, the metagenomic clock assigned a greater estimated age to individuals with type 1 diabetes, suggesting an association between microflora and metabolism (Galkin et al., 2020b). More work is needed to develop metabolomic and metagenomic aging clocks.

Despite the success of aging clocks, they inherit shortcomings from their training sets. One challenge is that the publicly available datasets used come in a variety of non-standardized formats, contain missing values, and often have no information on comorbidities. For example, a study on Alzheimer’s disease may include a mix of people with a range of comorbidities like diabetes, cancer, cardiovascular disease (Galkin et al., 2020a). Consequently, there is a need to use a multimodal approach when defining biological age. A comprehensive framework, including state-of-the-art -omics technologies, well-established and assessable clinical indicators, and physical and cognitive performance indices (Jansen et al., 2021; Sun et al., 2021; Mavromatis et al., 2023; McGreevy et al., 2023) are all needed. Advances in artificial intelligence (AI)-driven tools, including deep neural networks and convolutional neural networks, grasp non-linear relationships between biological features and accelerate both novel biomarker discovery and the proof-of-concept for newer aging clocks (Zhavoronkov et al., 2019; Galkin et al., 2021). One exciting application of AI to longevity research is the use of generative adversarial networks (GAN) for missing value imputation (a common problem with clinical datasets), and training set expansion (Galkin et al., 2020a). Once a patient’s biomarker blueprint is made, a GAN can be used to predict future changes in the patient’s biomarker profile—move it back and forth in time—and suggest custom geroprotective interventions (Zhavoronkov and Mamoshina, 2019). Overall, aging clocks improve our ability to estimate mortality and morbidity.

Comorbidities

One limitation to longevity is the presence of other diseases that truncate lifespan. Many longevity markers discussed so far measure the development of such diseases. For example, glucose measurements are used to diagnose diabetes; cholesterol and triglyceride levels are markers for cardiovascular disease; urinary creatinine and albumin measure kidney function (see Laboratory biomarkers). CRP and IL-6 measure acute phase responses to disease, and upregulate clotting factors; consequently, elevated IL-6 levels are associated with thrombosis and stroke (Ding et al., 2023). Hypertension, CRF are also used as longevity readouts (see Physiological biomarkers), whereas hearing acuity can signify cognitive decline (see Neurological biomarkers). Thus, longevity biomarkers overlap with the largest chronic diseases in the elderly worldwide (ischaemic heart disease, diabetes, stroke, chronic kidney disease, lung cancer, and age-related hearing loss) (GBD 2019 Diseases and Injuries Collaborators, 2020).

Since chronic diseases are tied into our measures of longevity, it becomes challenging to consider interventions expected to increase lifespan in individuals without the disease vs. reducing the proportion of these comorbidities in the population. On one hand, reducing chronic disease is relevant to longevity research, because it will directly impact longevity in affected individuals. On the other hand, biomarkers that measure chronic diseases may be of limited use for individuals without chronic disease. Thus, one challenge is determining the populations in which a given biomarker is most useful.

Two other challenges to measuring longevity are medical emergencies and acute infectious diseases. Minimizing both of these threats will improve lifespan because both increase with age. For example, falls are a leading cause of injury-related death in the elderly (CDC, 2024). Infectious diseases, such as urinary tract infections, lower respiratory tract infections, skin and soft tissue infections, intra-abdominal infections (cholecystitis, diverticulitis, appendicitis, abscesses), infective endocarditis, bacterial meningitis, tuberculosis, and herpes zoster, are prevalent in the elderly and three times as deadly as in young adult patients (Yoshikawa, 2000). On one hand, this reveals a need to track frailty (i.e. susceptibility to physical trauma), and immunity (i.e. susceptibility to infectious disease) with age. On the other hand, behavioral interventions (e.g. avoid stairs, precautions for disease), may reduce vulnerability and extend lifespan. Thus, tracking frailty and immunity may predict longevity in the population, but require adjustment at the individual level for utility.

One common factor in comorbidities that limit longevity is chronic inflammation (Furman et al., 2019). Chronic inflammation is the inability to resolve an inflammatory state; in contrast to acute inflammation, there is continual immune stimulation. In some cases, chronic inflammation occurs due to a failure to deal with pathogens. In other cases, chronic inflammation is due to the production of pro-inflammatory signals in the absence of pathogens, called “sterile inflammation” (Chen and Nunez, 2010). Examples of sterile inflammation include inflammation stimulated by uric acid (gout) (Martinon et al., 2006), and responses to proteins and nutrients (e.g. LDL) that get oxidized over time (atherosclerosis) (Libby et al., 2019). The association of chronic inflammation with limiting longevity is strong enough that a separate term was coined to better discuss the connections between aging phenotypes and inflammation: “inflamm-aging” (Franceschi et al., 2018). Typically inflamm-aging focuses on low-grade, sterile inflammation, but infectious origins are challenging to rule out.

Inflamm-aging has the potential to account for most deleterious aging phenotypes: pathway enrichment analysis showed that proteins implicated in inflammation and immune function are especially adept at predicting age (Lehallier et al., 2020). Additionally, inflamm-aging is linked to age-related sarcopenia (Liang et al., 2022), Alzheimer’s disease (Xia et al., 2016), gut microbiota (Franceschi et al., 2018), metabolic state (López-Otín et al., 2016; Franceschi et al., 2018), and disease resistance (Chambers and Akbar, 2020). All of these conditions associate with longevity. This creates a complex network of feedback loops that are challenging to sort out.

Therapeutic blocking of inflammation to extend longevity may require nuance. Notably, acute inflammation is necessary for fighting pathogens and limiting damage from them. As an extreme example, anti-inflammatory interventions during sepsis are more efficacious in patients with a higher risk of death, whereas in cases where subjects are likely to survive, disrupting well-regulated inflammatory pathways may weaken protective host defense mechanisms and lead to a worse outcome (Eichacker et al., 2002). This was tragically learned when the blockade of tumor necrosis factor alpha (TNF-α) caused increased mortality (Eichacker et al., 2002). Another challenge is that certain areas of the body require inflammation for proper function. For instance, low-grade steady-state inflammation has been shown to be essential for the co-existence of the host with the gut commensal microbiota (Varol et al., 2015; Schnell et al., 2023). Postnatal cyclic mammary gland remodeling, i.e. branching morphogenesis, also relies on macrophage recruitment and local homeostatic inflammation (Van Nguyen and Pollard, 2002; Varol et al., 2015).

Over the years, the focus on targeting inflammation has shifted from blocking it to promoting successful resolution (Buckley et al., 2013). Resolution of inflammation restores tissue homeostasis and is associated with pathways and interventions that may enhance longevity (Serhan and Levy, 2018). Thus, measuring both pro-inflammatory and pro-resolving markers may help us understand the balance between inflammation and health. Altogether, accounting for comorbidities remains one challenge when measuring and enhancing longevity.

Biomarker panels

With all of these different indicators of health and mortality, combining them may give a more holistic picture of an individual’s overall health. By combining multiple markers, panels can provide a more nuanced picture of an individual's health status and better report changes over time (Shamir, 2015). Finally, using multiple markers can reduce the variability and noise inherent in measurements of individual biomarkers. However, there are also challenges to using biomarker panels. One challenge is that the interpretation of biomarker panels can be complex and may require specialized expertise, especially if different markers contradict each other. Also, not all markers included in a panel may be relevant to all individuals, leading to unnecessary testing and increased costs. Overall, biomarker panels are a valuable tool to evaluate health and disease.
Choosing the optimal biomarker panel remains a complicated question. Several groups of biomarkers that reflect a) biological age, b) rate of aging, and c) risk of various age-related diseases may not give the same results. Logistic factors unrelated to aging also impact the choice of biomarkers. For example, biomarkers that have long been measured and are widely available (such as with a general blood test), have more years of longitudinal data, and are more affordable. Databases such as UK Biobank and NHANES provide large datasets suitable for robust analysis of biomarker behavior. However, if the biomarker is new, there may be limited data in human populations on that biomarker. Therefore, updates to new biomarkers may take years to validate. This complicates the development of consistent and wide use of biomarker panels.

The proliferation of wearable devices that measure biometric data like heart rate, sleep pattern, and exercise provides large amounts of longitudinal data. This may provide a simple set of markers to predict and measure longevity, i.e. “digital biomarkers” (Vasudevan et al., 2022). Parameters such as daily steps, heart rate variability, resting heart rate, exercise, blood oxygen saturation, and VO2max are collected throughout the day for millions of users. Many apps now include reminders, badges, and other tools to encourage people to achieve certain levels of activity. One current opportunity is developing AI algorithms to produce meaningful assessments using data from wearables (Acosta et al., 2022). The sheer amount of longitudinal, non-invasive data that can be generated provides an affordable and convenient approach for health-centered decision-making on longevity.

Along with physiological parameters that give overall estimates, some biomarker panels focus on assessing risk for key causes of mortality. Since one global leading cause of disability and death is cardiovascular disease (GBD 2019 Diseases and Injuries Collaborators, 2020; Tsao et al., 2023), biomarker panels that assess cardiovascular disease may also predict longevity. Composite scores based on blood biomarkers include the Framingham Risk Score (Wilson et al., 1998), and QRISK3 (Hippisley-Cox et al., 2017), which combine age, systolic blood pressure, smoking status, total cholesterol, and HDL cholesterol measurements (Fig 4). The Framingham Risk Score is predictive for longevity potential (with AUC = 64.7) (Beekman et al., 2016). When this score is combined with physiological parameters involved in immune responses, glucose, lipid, and energy metabolism, the prediction performance for longevity potential is further improved (up to AUC = 71.4) (Beekman et al., 2016). Thus, cardiovascular biomarker panels give a reasonable start to using biomarker panels to estimate longevity.

A modified approach to biomarker panels intended for both lay people and physicians is the Life’s Simple 7 panel, created by the American Heart Association (AHA). These guidelines focus on determining optimal cardiovascular health using seven different biomarkers and habits (Lloyd-Jones et al., 2010). The seven metrics are diet quality, amount of weekly physical activity, exposure to cigarette smoking, body mass index, fasting blood glucose, total cholesterol, and blood pressure (Lloyd-Jones et al., 2010). Each category is given descriptors (ideal, intermediate, or poor) for each metric based on accepted clinical thresholds. In a meta-analysis of 9 prospective cohort studies, having the highest number of ideal cardiovascular health metrics (generally ≥5 versus 0-2) was associated with a risk reduction of 0.20 for CVD (95% CI, 0.11-0.37), 0.31 for stroke (95% CI, 0.25-0.38), 0.25 for CVD mortality (95% CI, 0.10-0.63), and 0.55 for all-cause mortality (95% CI, 0.37-0.80) (Fang et al., 2016). Life’s Simple 7 predicts cardiovascular disease (CVD)-free survival, associates with overall longevity and higher quality of life (Lloyd-Jones et al., 2010). In 2022, this model was updated. These updates added sleep duration as an eighth component, replaced total cholesterol with total non-HDL cholesterol, and revamped the scoring system to a more intuitive range of 1-100. The new aggregate score, now called Life’s Essential 8 (LE8), calculates the unweighted average of all 8 component metric scores (Lloyd-Jones et al., 2022). In the new system, average cardiovascular scores are considered high (80-100), moderate (50-79), or low (0-49). Higher LE8 scores associate with both a lower risk of cardiovascular death and all-cause death (Isiozor et al., 2023; Sun et al., 2023). This framework provides a straightforward biomarker panel that can be used to improve overall health and early lifestyle interventions. Importantly, this biomarker panel is web accessible via the AHA page, and allows multiple measurements.

Along with LE8, other indices and scores may be used to predict and assess specific aspects of aging and risk of death (Table 1). For example, the degree of frailty can be measured by Fried’s frailty index (Fried et al., 2001), Charlson comorbidity index (Charlson et al., 1987), and Elixhauser comorbidity index (Elixhauser et al., 1998). Fried’s index measures frailty using weight loss, exhaustion, low physical activity, slowness, and weakness to assign people to three categories: not frail, pre-frail, and frail (Fried et al., 2001). The Charlson comorbidity index assigns scores based on 17 potential comorbidities plus age (Charlson et al., 1987), while the Elixhauser comorbidity index measures 30 (Elixhauser et al., 1998). While the Charlson index is easier to calculate, the Elixhauser index is more comprehensive and has greater statistical power (Sharma et al., 2021). While these indices are useful for the general population, they may not be helpful in predicting lifespan for individuals who are not frail and have few to no comorbidities. New panels are needed to measure these features.

Current approaches to biomarker panels need to consider many potential trade-offs. Ideally, such composite scores should be straightforward, easy and cheap to measure, require minimal collection effort, and display minimal operator variability. The age range and overall health status in which they operate are also important considerations. The goal for true longevity biomarkers (vs. markers of comorbidities) is to provide feedback into the aging process early enough to allow intervention, and to provide information on the success of those markers. Complementing bloodwork panels and epigenetic clocks with advances in artificial intelligence, machine learning, big data, statistics, and availability of health datasets will allow new types of "aging clocks" to be developed.

Understanding the myriad potential biomarkers, and their relative value remains an ongoing challenge. The longevity field gained momentum to specify key definitions and formalize the framework for the longevity-tailored biomarker identification and validation as surrogate endpoints in the clinical setting with the advent of the international panel of the Biomarkers of Aging Consortium (Moqri et al., 2023, 2024). Similarly, a different organization, the Aging Biomarkers Consortium (Ren et al., 2023), expressed its position on the biomarker landscape in a series of comprehensive reviews: on general biomarkers of aging (Aging Biomarker Consortium et al., 2023a), on specific biomarkers of cardiac aging (Aging Biomarker Consortium et al., 2023e), vascular aging (Aging Biomarker Consortium et al., 2023d), brain aging (Aging Biomarker Consortium et al., 2023b), skeletal aging (Aging Biomarker Consortium et al., 2023c). Thus, concerted worldwide efforts to formulate a roadmap to defining and implementing the most promising biomarkers for translational geriatric research have been initiated. In the wake of the “-omics” era, guidelines for multiomic integration of time-resolved molecular-genetic readouts, processed with the help of AI, have been published (Solovev et al., 2020; Rutledge et al., 2022), underscoring the importance of the data-first approach to biomarker mining and validation.

The computational toolbox at the field’s disposal has been augmented with several critical user-friendly solutions for deploying aging clocks in a standardized fashion, allowing the comparison of outputs across research formats and objectives: the pyaging (de Lima Camillo, 2024) and biolearn (Ying et al., 2024b) Python packages. Further, for no-code analysis of biomarker dynamics in large-cohort longitudinal studies, platforms such as ClockBase (Ying et al., 2023) (clockbase.org) and HALL (Li et al., 2024) (ngdc.cncb.ac.cn/hall/index), utilizing multidimensional data from publicly available repositories, such as GEO and NHANES, now exist.

Conclusion

There remains an outstanding need to identify robust biomarkers for longevity research. Here, we surveyed existing biomarkers that are useful, in our opinion, for assessing personal aging trajectories and predicting life- and healthspan. A generalizable foundation for biomarker evaluation yet to be created will aid researchers and the public to better consider what biomarkers they may choose to measure. We consolidated the current longevity biomarker trends, discussing their prospective functionality for predicting the number of disease-free years and time to death, i.e. prospective biomarkers, as compared to response biomarkers, which are those that are sensitive to longevity interventions and will be useful in the context of clinical trials (Cummings and Kritchevsky, 2022). As a result, we present a broad narrative on popular longevity biomarkers, their application and limitations, enabling informed choice for biomarker measurement.

Acknowledgments

We thank Alexey Strygin, Evgeni Bikov, Gherardo Baudo, and Susanne Neumann for their help in manuscript preparation; members of VitaDAO and ResearchHub for constructive feedback and helpful criticisms. We apologize to those authors whose work we were unable to cite due to space constraints.

Conflicts of interest

The authors are members of VitaDAO and ResearchHub, which commissioned this work.

Author contributions

Conceptualization: BTS, GN, VW, RA
Supervision: BTS, RA
Writing—original draft: BTS, RA
Writing—review & editing: BTS, GN, VW, RA
Figure preparation: RA

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Longevity biomarkers: applications and limitations

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Longevity biomarkers: applications and limitations

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