Evidence mapPaperPMID 40250404Full record

ReviewCell2025

From geroscience to precision geromedicine: Understanding and managing aging.

Guido Kroemer, Andrea B Maier, Ana Maria Cuervo, Vadim N Gladyshev, Luigi Ferrucci, Vera Gorbunova, Brian K Kennedy, Thomas A Rando, Andrei Seluanov, Felipe Sierra and 2 more

Abstract readReview
In one paragraph

Review in Cell, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 167 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
167citing papers in PubMed, 2 pooled it
field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

167 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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  6. Article
  7. Evolutionary genetics of ageing.Nature reviews. Genetics · 2026
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107 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Guido KroemerCentre de Recherche des Cordeliers, Equipe labellisée par la Ligue contre le cancer, Inserm U1138, Université Paris Cité, Sorbonne Université, Paris, France; Metabolomics and Cell Biology Platforms, Gustave Roussy Institut, Villejuif, France; Institut du Cancer Paris CARPEM, Department of Biology, Hôpital Européen Georges Pompidou, AP-HP, Paris, France. Electronic address: kroemer@orange.fr.
Andrea B MaierDepartment of Human Movement Sciences, @AgeAmsterdam, Faculty of Behavioural and Movement Sciences, Vrije Universiteit, Amsterdam Movement Sciences, Amsterdam, the Netherlands; NUS Academy for Healthy Longevity, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
Ana Maria CuervoDepartment of Developmental and Molecular Biology, Albert Einstein College of Medicine, Bronx, New York, NY 10461, USA; Institute for Aging Research, Albert Einstein College of Medicine, Bronx, New York, NY, USA; Department of Medicine, Albert Einstein College of Medicine, Bronx, New York, NY, USA.
Vadim N GladyshevBrigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Luigi FerrucciTranslational Gerontology Branch, National Institute on Aging Intramural Research Program, Baltimore, MD, USA.
Vera GorbunovaDepartment of Biology, University of Rochester, Rochester, NY, USA; Department of Medicine, University of Rochester Medical Center, Rochester, NY, USA.
Brian K KennedyHealthy Longevity Translational Research Program, Yong Loo Lin School of Medicine, Centre for Healthy Longevity, National University Health System, National University of Singapore, Singapore, Singapore; Life Sciences Institute Neurobiology Programme, Centre for Life Sciences, National University of Singapore, Singapore, Singapore; Departments of Biochemistry and Physiology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
Thomas A RandoDepartment of Neurology and Neurological Sciences, Stanford University School of Medicine, Stanford, CA, USA; Department of Neurology and Broad Stem Cell Research Center, University of California, Los Angeles, Los Angeles, CA, USA.
Andrei SeluanovDepartment of Biology, University of Rochester, Rochester, NY, USA; Department of Medicine, University of Rochester Medical Center, Rochester, NY, USA.
Felipe SierraHevolution Foundation, Riyadh, Saudi Arabia.
Eric VerdinBuck Institute for Research on Aging, Novato, CA, USA.
Carlos López-OtínCentre de Recherche des Cordeliers, Equipe labellisée par la Ligue contre le cancer, Inserm U1138, Université Paris Cité, Sorbonne Université, Paris, France; Facultad de Ciencias de la Vida y la Naturaleza, Universidad Nebrija, Madrid, Spain. Electronic address: clo@uniovi.es.

Funding

Role of Retrotransposon Activity in Neurodegeneration and Alzheimer's DiseaseP01AG051449 · NIA · BROWN UNIVERSITY · 2022 to 2025
$16.2M
Primary Cells, Tissues, and Animals CoreP01AG047200 · UNIVERSITY OF ROCHESTER · 2025 to 2025
$3.6M
Regulation of epigenome stability by SIRT6 during AgingR37AG046320 · UNIVERSITY OF ROCHESTER · 2025 to 2025
$679k
Understanding Interorgan Communication Through Heterochronic Organ TransplantationU01AG086168 · BRIGHAM AND WOMEN'S HOSPITAL · 2025 to 2025
$672k
Epigenetic Reprogramming of Cellular AgeR01AG071783 · UNIVERSITY OF CALIFORNIA LOS ANGELES · 2025 to 2025
$425k
Genomic Instability as A Driver of Stem Cell ExhaustionR01AG082764 · UNIVERSITY OF CALIFORNIA LOS ANGELES · 2025 to 2025
$424k
THE BALTIMORE LONGITUDINAL STUDY OF HUMAN AGINGZ01AG000015 · AGING · 1985 to 2005
Intramural NIH HHS Z01 AG000015Intramural NIH HHS Z01 AG000971NIAMS NIH HHS R33 AR078093NIA NIH HHS P01 AG047200NIA NIH HHS P01 AG051449NIA NIH HHS R01 AG046320NIA NIH HHS R01 AG071783NIA NIH HHS R01 AG082764NIA NIH HHS R37 AG046320NIA NIH HHS U01 AG086168Wellcome Trust
6 · The paper itself

Abstract

Major progress has been made in elucidating the molecular, cellular, and supracellular mechanisms underlying aging. This has spurred the birth of geroscience, which aims to identify actionable hallmarks of aging. Aging can be viewed as a process that is promoted by overactivation of gerogenes, i.e., genes and molecular pathways that favor biological aging, and alternatively slowed down by gerosuppressors, much as cancers are caused by the activation of oncogenes and prevented by tumor suppressors. Such gerogenes and gerosuppressors are often associated with age-related diseases in human population studies but also offer targets for modeling age-related diseases in animal models and treating or preventing such diseases in humans. Gerogenes and gerosuppressors interact with environmental, behavioral, and psychological risk factors to determine the heterogeneous trajectory of biological aging and disease manifestation. New molecular profiling technologies enable the characterization of gerogenic and gerosuppressive pathways, which serve as biomarkers of aging, hence inaugurating the era of precision geromedicine. It is anticipated that, pending results from randomized clinical trials and regulatory approval, gerotherapeutics will be tailored to each person based on their genetic profile, high-dimensional omics-based biomarkers of aging, clinical and digital biomarkers of aging, psychosocial profile, and past or present exposures.

Indexed as

AgingGeriatricsGerosciencePrecision MedicineAnimalsHumansagingaging clocksanti-aging drugsatherosclerosiscancercardiovascular diseasesdiabetesepigenetic clocksgenomicsneurodegenerationoncogeneoncosuppressionprimary prevention

Identifiers

PMID40250404
PMCPMC12037106

What Socratic holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.