Effect of long-term caloric restriction on DNA methylation measures of biological aging in healthy adults from the CALERIE trial DOI Creative Commons
Reem Waziry, Calen P. Ryan, David L. Corcoran

et al.

Nature Aging, Journal Year: 2023, Volume and Issue: unknown

Published: Feb. 9, 2023

The geroscience hypothesis proposes that therapy to slow or reverse molecular changes occur with aging can delay prevent multiple chronic diseases and extend healthy lifespan

Language: Английский

Quantification of the pace of biological aging in humans through a blood test, the DunedinPoAm DNA methylation algorithm DOI Creative Commons
Daniel W. Belsky, Avshalom Caspi, Louise Arseneault

et al.

eLife, Journal Year: 2020, Volume and Issue: 9

Published: May 5, 2020

Biological aging is the gradual, progressive decline in system integrity that occurs with advancing chronological age, causing morbidity and disability. Measurements of pace are needed as surrogate endpoints trials therapies designed to prevent disease by slowing biological aging. We report a blood-DNA-methylation measure sensitive variation among individuals born same year. first modeled change-over-time 18 biomarkers tracking organ-system across 12 years follow-up n = 954 members Dunedin Study 1972–1973. Rates change each biomarker over ages 26–38 were composited form aging-related decline, termed Pace-of-Aging. Elastic-net regression was used develop DNA-methylation predictor Pace-of-Aging, called DunedinPoAm for Dunedin(P)ace(o)f(A)ging(m)ethylation. Validation analysis cohort studies CALERIE trial provide proof-of-principle single-time-point person’s

Language: Английский

Citations

410

A systematic review of biological, social and environmental factors associated with epigenetic clock acceleration DOI Creative Commons
Lara Oblak, Jeroen van der Zaag, Albert Higgins‐Chen

et al.

Ageing Research Reviews, Journal Year: 2021, Volume and Issue: 69, P. 101348 - 101348

Published: April 28, 2021

Aging involves a diverse set of biological changes accumulating over time that leads to increased risk morbidity and mortality. Epigenetic clocks are now widely used quantify aging, in order investigate determinants modify the rate aging predict age-related outcomes. Numerous biological, social environmental factors have been investigated for their relationship epigenetic clock acceleration deceleration. The aim this review was synthesize general trends concerning associations between human these factors. We conducted systematic all available literature included 156 publications across 4 resource databases. compiled list presently existing blood-based clocks. Subsequently, we created an extensive dataset 1300 study findings which were utilized blood tissue subjects assess numeral exposures traits. Statistical analysis possible on 57 such relationships, measured different (Hannum, Horvath, Levine GrimAge). found Hannum, GrimAge tend agree direction effects, but vary size. Body mass index, HIV infection, male sex significantly associated with one or more Acceleration also related mortality, cardiovascular disease, cancer diabetes. Our provide graphical numerical synopsis past decade age estimation research indicate areas where further attention could be focused coming years.

Language: Английский

Citations

398

Hallmarks of Health DOI Creative Commons
Carlos López‐Otín, Guido Kroemer

Cell, Journal Year: 2020, Volume and Issue: 184(1), P. 33 - 63

Published: Dec. 18, 2020

Language: Английский

Citations

376

Telomere Length as a Marker of Biological Age: State-of-the-Art, Open Issues, and Future Perspectives DOI Creative Commons
Alexander Vaiserman, Dmytro Krasnienkov

Frontiers in Genetics, Journal Year: 2021, Volume and Issue: 11

Published: Jan. 21, 2021

Telomere shortening is a well-known hallmark of both cellular senescence and organismal aging. An accelerated rate telomere attrition also common feature age-related diseases. Therefore, length (TL) has been recognized for long time as one the best biomarkers Recent research findings, however, indicate that TL per se can only allow rough estimate aging hardly be regarded clinically important risk marker pathologies mortality. Evidence obtained other indicators such certain immune parameters, indices epigenetic age, etc., could stronger predictors health status chronic disease. However, despite these issues limitations, remains to very informative in accessing biological age when used along with markers homeostatic dysregulation, frailty index, clock, etc. This review article aimed at describing current state art field discussing recent findings divergent viewpoints regarding usefulness leukocyte estimating human age.

Language: Английский

Citations

311

Measuring biological age using omics data DOI
Jarod Rutledge, Hamilton Oh, Tony Wyss‐Coray

et al.

Nature Reviews Genetics, Journal Year: 2022, Volume and Issue: 23(12), P. 715 - 727

Published: June 17, 2022

Language: Английский

Citations

301

Heterogeneous aging across multiple organ systems and prediction of chronic disease and mortality DOI Open Access
Ye Tian, Vanessa Cropley, Andrea B. Maier

et al.

Nature Medicine, Journal Year: 2023, Volume and Issue: 29(5), P. 1221 - 1231

Published: April 6, 2023

Language: Английский

Citations

270

Biomarkers of aging for the identification and evaluation of longevity interventions DOI Creative Commons
Mahdi Moqri, Chiara Herzog, Jesse R. Poganik

et al.

Cell, Journal Year: 2023, Volume and Issue: 186(18), P. 3758 - 3775

Published: Aug. 1, 2023

Language: Английский

Citations

262

Tau Post-translational Modifications: Dynamic Transformers of Tau Function, Degradation, and Aggregation DOI Creative Commons
Carolina Alquézar, Shruti Arya, Aimee W. Kao

et al.

Frontiers in Neurology, Journal Year: 2021, Volume and Issue: 11

Published: Jan. 7, 2021

Post-translational modifications (PTMs) on tau have long been recognized as affecting protein function and contributing to neurodegeneration. The explosion of information potential observed PTMs provides an opportunity better understand these in the context homeostasis, which becomes perturbed with aging disease. Prevailing views regard a that undergoes abnormal phosphorylation prior its accumulation into toxic aggregates implicated Alzheimer's disease (AD) other tauopathies. However, may, fact, represent part normal but interrupted catabolism protein. In addition phosphorylation, another forms post-translational modification including (but not limited to), acetylation, ubiquitination, glycation, glycosylation, SUMOylation, methylation, oxidation, nitration. A holistic appreciation how regulate during health are potentially hijacked remains elusive. Recent studies reinforced idea play critical role localization, protein-protein interactions, maintenance levels, modifying aggregate structure. These also provide tantalizing clues possibility neurons actively choose is post-translationally modified, competitive combinatorial ways, achieve broad, cellular programs commensurate distinctive environmental conditions found development, aging, stress, Here, we review describe what currently known about their functional impacts. addition, classify from perspectives electrostatics, stability, all contribute homeostasis. Finally, assess impact solubility aggregation. Tau occupies undoubtedly important position biology neurodegenerative diseases. This aims integrated perspective actively, purposefully, dynamically remodel function, clearance, doing so, hope enable more comprehensive understanding will positively future studies.

Language: Английский

Citations

243

The landscape of aging DOI Open Access
Yusheng Cai, Wei Song, Jiaming Li

et al.

Science China Life Sciences, Journal Year: 2022, Volume and Issue: 65(12), P. 2354 - 2454

Published: Sept. 2, 2022

Language: Английский

Citations

240

A computational solution for bolstering reliability of epigenetic clocks: implications for clinical trials and longitudinal tracking DOI
Albert Higgins‐Chen, Kyra Thrush, Yunzhang Wang

et al.

Nature Aging, Journal Year: 2022, Volume and Issue: 2(7), P. 644 - 661

Published: July 15, 2022

Language: Английский

Citations

238