Evidence map›Paper›PMID 20926537›Full record

ReviewThe Journal of clinical endocrinology and metabolism2010

Genetic studies reveal the role of the endocrine and metabolic systems in aging.

Nir Barzilai, Ilan Gabriely, Gil Atzmon, Yousin Suh, Devorah Rothenberg, Aviv Bergman

Erratum issuedAbstract readReview
In one paragraph

Review in The Journal of clinical endocrinology and metabolism, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 37 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 1 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

37 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Review
  13. Aging, inflammation and the environment.Experimental gerontology · 2018
    Review
  14. Article
  15. Informing Prevention and Intervention Policy Using Genetic Studies of Resistance.Prevention science : the official journal of the Society for Prevention Research · 2018
    Article
  16. Activation-Induced Autophagy Is Preserved in CD4+ T-Cells in Familial Longevity.The journals of gerontology. Series A, Biological sciences and medical sciences · 2017
    Article
  17. Review
  18. Article
  19. Genetic mutations you want.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  20. Relationship between Oxidative Stress, Circadian Rhythms, and AMD.Oxidative medicine and cellular longevity · 2016
    Review
4 · The record

Corrections and comments

  • Erratum issued
    Atzmon, Gil [added]; Suh, Yousin [added]; Rothenberg, Devorah [added]; Bergman, Aviv [added]
5 · Who and what money

Authors and funding

6 authors.

Nir BarzilaiDepartment of Medicine, Albert Einstein College of Medicine, Bronx, New York 10461, USA.
Ilan Gabriely
Gil Atzmon
Yousin Suh
Devorah Rothenberg
Aviv Bergman

Funding

Stable Isotope and Metabolomics CoreP60DK020541 · NIDDK · YESHIVA UNIVERSITY · PI FLEISCHER, NORMAN S. · 1986 to 2014
$29.8M
Translational Research CoreP30DK020541 · NIDDK · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI STREAMSON C CHUA · 2015 to 2026
$27.7M
WEIGHT MGT &NUTRITION FOR PRE-/PERIMENOPAUSAL BREAST CANCER SURVIVORSM01RR012248 · NCRR · YESHIVA UNIVERSITY · PI CRANDALL, JILL P · 1997 to 2008
$18.4M
STATISTICS AND DATA MANAGEMENT COREP01AG027734 · NIA · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI BARZILAI, NIR J · 2007 to 2012
$9.3M
Longevity Genes in Founder PopulationsR01AG018728 · NIA · UNIVERSITY OF MARYLAND BALTIMORE · PI SHULDINER, ALAN R. · 2001 to 2005
$3.8M
MECHANISMS OF CELLULAR IMMORTALIZATIONR01AG007992 · NIA · UT SOUTHWESTERN MEDICAL CENTER · PI WRIGHT, WOODRING ERIK · 1989 to 2010
$3.3M
A Systems Methodology for the Biology of AgingR01AG028872 · NIA · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI BERGMAN, AVIV · 2007 to 2011
$1.8M
Association Analysis- SNPs in Longevity Assurance GenesR01AG024391 · NIA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI SUH, YOUSIN · 2004 to 2008
$1.6M
NCRR NIH HHS M01 RR012248NCRR NIH HHS M01-RR12248NIA NIH HHS P01 AG027734NIA NIH HHS R01 AG007992NIA NIH HHS R01 AG018728NIA NIH HHS R01 AG024391NIA NIH HHS R01-AG028872NIA NIH HHS R01 AG-18728-01A1NIA NIH HHS R01 AG7992NIDDK NIH HHS DK 20541NIDDK NIH HHS P30 DK020541NIDDK NIH HHS P60 DK020541
6 · The paper itself

Abstract

Aging is a natural process that involves a general decline in many physiological functions, resulting in loss of function and eventually death. Extensive research is being performed in order to elucidate the biology of aging, especially with the advent of newer molecular and genetic methodologies. The endocrine system plays a major role in orchestrating cellular interactions, metabolism, growth, and senescence. Thus, researchers traditionally used hormones as tools to induce and examine specific biological effects that are associated with aging. Furthermore, because our recent knowledge on hormonal action expanded significantly, downstream pathways and genetic determinants currently prevail in aging research. In this review, we will summarize the effects of several hormones on human aging and longevity and present recent data from the Longevity Genes Study performed at Albert Einstein College of Medicine, looking at the phenotype and genotype of centenarians and their offspring. We will demonstrate that genetic factors that are associated with human longevity are heritable and may contribute not only to quantitative longevity but also to protection from age-dependent disease and exceptional good health.

Indexed as

AgingEndocrine SystemGenetic Association StudiesGenetics, PopulationGenotypeHumansLongevityMetabolismPhenotype

Identifiers

PMID20926537
PMCPMC3050096

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.