Evidence map›Paper›PMID 17677003›Full record

ReviewPLoS genetics2007

Genetic determinants of human health span and life span: progress and new opportunities.

George M Martin, Aviv Bergman, Nir Barzilai

Abstract readReview
In one paragraph

Review in PLoS genetics, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing 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.

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

60 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Measuring biological age using omics data.Nature reviews. Genetics · 2022
    Review
  5. Review
  6. Protective Effects of Familial Longevity Decrease With Age and Become Negligible for Centenarians.The journals of gerontology. Series A, Biological sciences and medical sciences · 2022
    Article
  7. Article
  8. Review
  9. Article
  10. Biogerontology: research status, challenges and opportunities.Acta bio-medica : Atenei Parmensis · 2018
    Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. The Economic Promise of Delayed Aging.Cold Spring Harbor perspectives in medicine · 2015
    Review
  17. Article
  18. Article
  19. Article
  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

3 authors.

George M MartinDepartment of Pathology, University of Washington, Seattle, Washington, United States of America. gmmartin@u.washington.edu
Aviv Bergman
Nir Barzilai

Funding

THERAPEUTIC EFFECTS OF INTRA-NASAL INSULIN DETEMIRP50AG005136 · NIA · UNIVERSITY OF WASHINGTON · PI WIJSMAN, ELLEN M · 1985 to 2019
$57.2M
SPECIFICITY OF OXYGEN DNA DAMAGE AND MUTAGENESISP01AG001751 · NIA · UNIVERSITY OF WASHINGTON · PI RABINOVITCH, PETER S · 1985 to 2021
$29.6M
Functional and Health Changes of the ElderlyU01AG007198 · NIA · DUKE UNIVERSITY · PI MANTON, KENNETH G. · 2003 to 2006
$12.7M
ROLE OF NUTRIENTS IN AGE-RELATED INSULIN RESISTANCEP01AG021654 · NIA · YESHIVA UNIVERSITY · PI HAWKINS, MEREDITH A · 2003 to 2007
$10.6M
DYSREGULATION OF GLUCOSE HOMEOSTASIS IN AGINGR01AG018381 · NIA · YESHIVA UNIVERSITY · PI BARZILAI, NIR J · 2000 to 2009
$3.2M
INTERNATIONAL REGISTRY OF WERNER SYNDROME/CELL BANKR24CA078088 · NCI · UNIVERSITY OF WASHINGTON · PI MARTIN, GEORGE M. · 1997 to 2011
$2.1M
dementias of the Alzheimer's TypeR01AG019711 · NIA · UNIVERSITY OF WASHINGTON · PI MARTIN, GEORGE M. · 2001 to 2005
$1.6M
NCI NIH HHS R24 CA078088NCI NIH HHS R24CA078088NIA NIH HHS P01 AG001751NIA NIH HHS P01 AG01751NIA NIH HHS P01 AG021654NIA NIH HHS P01AG021654NIA NIH HHS P30 AG01751NIA NIH HHS P50 AG005136NIA NIH HHS P50 AG05136-17NIA NIH HHS R01 AG018381NIA NIH HHS R01AG018381NIA NIH HHS R01 AG019711NIA NIH HHS R01AG019711NIA NIH HHS U01 AG007198NIA NIH HHS U01 AG 07198
6 · The paper itself

Abstract

We review three approaches to the genetic analysis of the biology and pathobiology of human aging. The first and so far the best-developed is the search for the biochemical genetic basis of varying susceptibilities to major geriatric disorders. These include a range of progeroid syndromes. Collectively, they tell us much about the genetics of health span. Given that the major risk factor for virtually all geriatric disorders is biological aging, they may also serve as markers for the study of intrinsic biological aging. The second approach seeks to identify allelic contributions to exceptionally long life spans. While linkage to a locus on Chromosome 4 has not been confirmed, association studies have revealed a number of significant polymorphisms that impact upon late-life diseases and life span. The third approach remains theoretical. It would require longitudinal studies of large numbers of middle-aged sib-pairs who are extremely discordant or concordant for their rates of decline in various physiological functions. We can conclude that there are great opportunities for research on the genetics of human aging, particularly given the huge fund of information on human biology and pathobiology, and the rapidly developing knowledge of the human genome.

Indexed as

AgingHealth StatusLife ExpectancyAllelesChromosome MappingGenetic LinkageGenome, HumanHealthHumansLongevityModels, GeneticPolymorphism, GeneticProgeriaRisk FactorsSyndrome

Identifiers

PMID17677003
PMCPMC1934400

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.