Evidence map›Paper›PMID 34498278›Full record

ArticleAnnals of the New York Academy of Sciences2022

Extending human healthspan and longevity: a symposium report.

Loren M DeVito, Nir Barzilai, Ana Maria Cuervo, Laura J Niedernhofer, Sofiya Milman, Morgan Levine, Daniel Promislow, Luigi Ferrucci, George A Kuchel, Joan Mannick and 5 more

Registry-linked trialAbstract readConference Proceedings
In one paragraph

Article in Annals of the New York Academy of Sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00707694 (Searching for Longevity Genes in the Historically Unique Ashkenazi Jewish Population), which is not on this map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
–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.

NCT00707694 recruitingnot on this map

Searching for Longevity Genes in the Historically Unique Ashkenazi Jewish Population

TypeobservationalSponsorAlbert Einstein College of MedicineRan1998 to 2032Enrolled2,000ConditionsExtreme Longevity
3 · Its place in the literature

Who cites it

30 citing papers in PubMed.

  1. Trial
  2. Article
  3. Associations of common infections with frailty and mortality in two UK cohort studies.The journals of gerontology. Series A, Biological sciences and medical sciences · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Exercise attenuates the hallmarks of aging: Novel perspectives.Journal of sport and health science · 2025
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. Article
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

15 authors.

Loren M DeVitoSticky Ink, Inc, New York, New York.
Nir BarzilaiAlbert Einstein College of Medicine, Bronx, New York.
Ana Maria CuervoAlbert Einstein College of Medicine, Bronx, New York.
Laura J NiedernhoferUniversity of Minnesota Medical School, Minneapolis, Minnesota.
Sofiya MilmanAlbert Einstein College of Medicine, Bronx, New York.
Morgan LevineYale School of Medicine, New Haven, Connecticut.
Daniel PromislowUniversity of Washington, Seattle, Washington.
Luigi FerrucciNational Institute on Aging, National Institutes of Health, Bethesda, Maryland.
George A KuchelUniversity of Connecticut School of Medicine, Farmington, Connecticut.
Joan MannickLife Biosciences, Boston, Massachusetts.
Jamie JusticeWake Forest School of Medicine, Winston-Salem, North Carolina.
Mitzi M GonzalesUniversity of Texas Health Sciences Center San Antonio, San Antonio, Texas.
James L KirklandMayo Clinic, Rochester, Minnesota.
Pinchas CohenUSC Leonard Davis School of Gerontology, Los Angeles, California.
Judith CampisiThe Buck Institute for Research on Aging, Novato, California.

Funding

Role of Autophagy in T Cell Function and Immunosenescence (Project 3)P01AG031782 · NIA · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI SINGH, RAJAT · 2009 to 2024
$36.2M
Validation and characterization of the identified variants associated with human longevity in mouse modelsU19AG056278 · NIA · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI Zhengdong Zhang · 2017 to 2026
$24.5M
San Antonio OAIC - Research Education Component (REC)P30AG044271 · NIA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Adam Salmon · 2015 to 2026
$14.1M
Role of the Mitochondrial Peptide Humanin in Regulating Aging and HealthspanP01AG055369 · NIA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI LONGO, VALTER D. · 2018 to 2023
$12.4M
PROTEOMICSP01AG043376 · NIA · UNIVERSITY OF MINNESOTA · PI ROBBINS, PAUL D. · 2013 to 2019
$11.2M
Einstein's Nathan Shock Center of Excellence in Basic Biology of AgingP30AG038072 · NIA · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI HUFFMAN, DEREK MAJOR · 2010 to 2024
$10.8M
USC-Buck Institute Nathan Shock Admin CoreP30AG068345 · NIA · BUCK INSTITUTE FOR RESEARCH ON AGING · PI LITHGOW, GORDON J · 2020 to 2024
$5.0M
Decreased Protein Degradation in AgingR37AG021904 · NIA · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI CUERVO, ANA MARIA · 2013 to 2022
$4.4M
Somatotropic Signaling and Resilience to Aging and Alzheimer's DiseaseR01AG061155 · NIA · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI MILMAN, SOFIYA · 2019 to 2023
$4.3M
DECREASED PROTEIN DEGRADATION IN AGINGR01AG021904 · NIA · YESHIVA UNIVERSITY · PI CUERVO, ANA MARIA · 2003 to 2012
$3.7M
Ethnic-specific Effects of Mitochondrial DNA Variants and Environmental Factors on Cognitive Functioning and DementiaR01AG068405 · NIA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI COHEN, PINCHAS, CRIMMINS, EILEEN M · 2020 to 2024
$3.6M
Using the senolytic fisetin to suppress mortality in aged mice acutely exposed to murine beta-coronavirusR01AG063543 · NIA · UNIVERSITY OF MINNESOTA · PI NIEDERNHOFER, LAURA JANE · 2019 to 2023
$3.4M
NIA NIH HHS K23 AG051148NIA NIH HHS P01 AG031782NIA NIH HHS P01 AG043376NIA NIH HHS P01 AG055369NIA NIH HHS P30 AG038072NIA NIH HHS P30 AG044271NIA NIH HHS P30 AG068345NIA NIH HHS R01 AG021904NIA NIH HHS R01 AG061155NIA NIH HHS R01 AG061165NIA NIH HHS R01 AG063543NIA NIH HHS R01 AG068405NIA NIH HHS R01 AG069698NIA NIH HHS R37 AG021904NIA NIH HHS RF1 AG061834NIA NIH HHS U19 AG056278
6 · The paper itself

Abstract

For many years, it was believed that the aging process was inevitable and that age-related diseases could not be prevented or reversed. The geroscience hypothesis, however, posits that aging is, in fact, malleable and, by targeting the hallmarks of biological aging, it is indeed possible to alleviate age-related diseases and dysfunction and extend longevity. This field of geroscience thus aims to prevent the development of multiple disorders with age, thereby extending healthspan, with the reduction of morbidity toward the end of life. Experts in the field have made remarkable advancements in understanding the mechanisms underlying biological aging and identified ways to target aging pathways using both novel agents and repurposed therapies. While geroscience researchers currently face significant barriers in bringing therapies through clinical development, proof-of-concept studies, as well as early-stage clinical trials, are underway to assess the feasibility of drug evaluation and lay a regulatory foundation for future FDA approvals in the future.

Indexed as

AgingGeroscienceLongevityResearch ReportAutophagyCardiovascular DiseasesHumansMetabolomicsNervous System DiseasesStem Cell Transplantationbiological aginggerosciencehallmarks of aginghealthspanlongevity

Identifiers

PMID34498278
PMCPMC10231756

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Registered trials

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 OpenQuestion graph.