Evidence map›Paper›PMID 22499766›Full record

ReviewThe journals of gerontology. Series A, Biological sciences and medical sciences2012

The search for longevity and healthy aging genes: insights from epidemiological studies and samples of long-lived individuals.

Joanne M Murabito, Rong Yuan, Kathryn L Lunetta

Abstract readReview
In one paragraph

Review in The journals of gerontology. Series A, Biological sciences and medical sciences, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 101 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
101citing papers in PubMed, 3 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

101 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. GWAS of longevity in CHARGE consortium confirms APOE and FOXO3 candidacy.The journals of gerontology. Series A, Biological sciences and medical sciences · 2015
    Pooled it
  4. Trial
  5. Review
  6. Article
  7. Article
  8. Article
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  11. Machine vision based frailty assessment for genetically diverse mice.bioRxiv : the preprint server for biology · 2024
    Article
  12. Article
  13. Review
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  16. Article
  17. Futurization of Aging: Subjective Beliefs and Effects.Behavioral sciences (Basel, Switzerland) · 2022
    Article
  18. Article
  19. Article
  20. Article

41 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

3 authors.

Joanne M MurabitoFramingham Heart Study, National Heart, Lung, and Blood Institute, Framingham, MA 01702, USA. murabito@bu.edu
Rong Yuan
Kathryn L Lunetta

Funding

Translational CoreP30AG038070 · NIA · JACKSON LABORATORY · PI John Matthew Mahoney · 2010 to 2026
$19.3M
Exceptional Aging Across the Life Span: Framingham StudyR01AG029451 · NIA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI MURABITO, JOANNE M · 2008 to 2011
$1.3M
Genetic Regulation of Circulating IGF1R21AG034349 · NIA · JACKSON LABORATORY · PI YUAN, RONG · 2010 to 2011
$397k
NIA NIH HHS AG034349NIA NIH HHS P30 AG038070NIA NIH HHS R01 AG029451NIA NIH HHS R01AG29451NIA NIH HHS R21 AG034349
6 · The paper itself

Abstract

Genetic factors clearly contribute to exceptional longevity and healthy aging in humans, yet the identification of the underlying genes remains a challenge. Longevity is a complex phenotype with modest heritability. Age-related phenotypes with higher heritability may have greater success in gene discovery. Candidate gene and genome-wide association studies (GWAS) for longevity have had only limited success to date. The Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium conducted a meta-analysis of GWAS data for longevity, defined as survival to age 90 years or older, that identified several interesting associations but none achieved genome-wide significance. A recent GWAS of longevity conducted in the Leiden Longevity Study identified the ApoE E4 isoform as deleterious to longevity that was confirmed in an independent GWAS of long-lived individuals of German descent. Notably, no other genetic loci for longevity have been identified in these GWAS. To examine the conserved genetic mechanisms between the mouse and humans for life span, we mapped the top Cohorts for Heart and Aging Research in Genomic Epidemiology GWAS associations for longevity to the mouse chromosomal map and noted that eight of the ten top human associations were located within a previously reported mouse life-span quantitative trait loci. This work suggests that the mouse and human may share mechanisms leading to aging and that the mouse model may help speed the understanding of how genes identified in humans affect the biology of aging. We expect these ongoing collaborations and the translational work with basic scientists to accelerate the identification of genes that delay aging and promote a healthy life span.

Indexed as

Aged, 80 and overAgingAnimalsDiseaseFemaleGenetic Association StudiesGenetic Predisposition to DiseaseGenome, HumanGenome-Wide Association StudyHumansLongevityMalePhenotypeRisk AssessmentRisk Factors

Identifiers

PMID22499766
PMCPMC3326242

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.