Evidence map›Paper›PMID 26297941›Full record

ArticleThe journals of gerontology. Series A, Biological sciences and medical sciences2016

Measures of Healthspan as Indices of Aging in Mice-A Recommendation.

Arlan Richardson, Kathleen E Fischer, John R Speakman, Rafael de Cabo, Sarah J Mitchell, Charlotte A Peterson, Peter Rabinovitch, Ying A Chiao, George Taffet, Richard A Miller and 7 more

Open access · bronzeAbstract read
In one paragraph

Article in The journals of gerontology. Series A, Biological sciences and medical sciences, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed, 3 pooled it
4.8field-weighted citation impact, top 4% of its field
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

53 citing papers in PubMed, 3 syntheses or guidelines pooled it, 84 citations in OpenAlex.

  1. Interventions that prolong multidimensional healthspan in humans: a systematic review of randomized controlled trials.The journals of gerontology. Series A, Biological sciences and medical sciences · 2026
    Pooled it
  2. Pooled it
  3. Pooled it
  4. Trial
  5. Article
  6. Review
  7. Physiological Systems in Promoting Frailty.Comprehensive Physiology · 2022
    Review
  8. Article
  9. Article
  10. New Directions in Research on Aging.Stem cell reviews and reports · 2022
    Article
  11. Sex Differences in the Relation Between Frailty and Endothelial Dysfunction in Old Mice.The journals of gerontology. Series A, Biological sciences and medical sciences · 2022
    Article
  12. Article
  13. Article
  14. Article
  15. The Second Annual Symposium of the Midwest Aging Consortium: The Future of Aging Research in the Midwestern United States.The journals of gerontology. Series A, Biological sciences and medical sciences · 2021
    Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 8 institutions in 1 country.

Arlan RichardsonDepartment of Geriatric Medicine, University of Oklahoma Health Science Center. Oklahoma City VA Medical Center. arlan-richardson@ouhsc.edu.
Kathleen E FischerDepartment of Biology, University of Alabama at Birmingham.
John R SpeakmanUniversity of Aberdeen, UK. State Key Laboratory of Molecular Developmental Biology, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, China.
Rafael de CaboTranslational Gerontology Branch, National Institute on Aging, Baltimore, Maryland.
Sarah J MitchellTranslational Gerontology Branch, National Institute on Aging, Baltimore, Maryland.
Charlotte A PetersonCollege of Health Sciences, University of Kentucky, Lexington.
Peter RabinovitchDepartment of Pathology, University of Washington, Seattle.
Ying A ChiaoDepartment of Pathology, University of Washington, Seattle.
George TaffetSection of Cardiovascular Research, Department of Medicine, Baylor College of Medicine, Houston, Texas.
Richard A MillerDepartment of Pathology and Geriatrics Center, University of Michigan, Ann Arbor.
René C RenteríaDepartment of Ophthalmology, Department of Health Restoration, and Care Systems Management and Center for Biomedical Neuroscience, University of Texas Health Science Center at San Antonio.
James BowerDepartment of Computer Science, University of California Santa Cruz.
Donald K IngramNutritional Neuroscience and Aging Laboratory, Pennington Biomedical Research Center, Louisiana State University, Baton Rouge.
Warren C LadigesDepartment of Comparative Medicine, University of Washington, Seattle.
Yuji IkenoDepartment of Pathology, University of Texas Health Science Center at San Antonio.
Felipe SierraBiology of Aging Program, National Institute on Aging, Bethesda, Maryland.
Steven N AustadDepartment of Biology, University of Alabama at Birmingham.
National Institute on Aging · USUniversity of Washington · USUniversity of Alabama at Birmingham · USBaylor College of Medicine · USThe University of Texas Health Science Center at San Antonio · USUniversity of California, Santa Cruz · USUniversity of Kentucky · USUniversity of Michigan–Ann Arbor · US

Funding

Systems BiologyU19AG023122 · NIA · TRANSLATIONAL GENOMICS RESEARCH INST · PI FRED H GAGE · 2004 to 2026
$102.6M
TRANSGENIC COREP30AG013319 · NIA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI JAMES FLOYD NELSON · 1995 to 2026
$30.6M
SPECIFICITY OF OXYGEN DNA DAMAGE AND MUTAGENESISP01AG001751 · NIA · UNIVERSITY OF WASHINGTON · PI PRUSKY, GLEN THOMAS · 1985 to 2021
$29.6M
Research Education CoreP30AG024824 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Neil Alexander · 2004 to 2026
$29.2M
Center for Testing Potential Anti-Aging InterventionsU01AG022307 · NIA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI RANDY STRONG, Adam Salmon · 2004 to 2026
$26.3M
Laboratory for Anti-Geric Testing, Evaluation and ResearchU01AG022303 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI RICHARD A MILLER · 2003 to 2026
$25.4M
GENETIC APPROACHES TO AGING RESEARCHT32AG000057 · NIA · UNIVERSITY OF WASHINGTON · PI RABINOVITCH, PETER S · 1985 to 2019
$14.2M
Aging Intervention ProgramZIAAG000363 · NIA · NATIONAL INSTITUTE ON AGING · PI DE CABO, RAFAEL · 2009 to 2025
$9.0M
Longevity genes and calorie restriction: early post-natal effectsR01AG019899 · NIA · SOUTHERN ILLINOIS UNIVERSITY SCH OF MED · PI BARTKE, ANDRZEJ · 2001 to 2016
$6.1M
Study of Longitudinal Aging in MiceZIAAG000335 · NIA · NATIONAL INSTITUTE ON AGING · PI DE CABO, RAFAEL · 2017 to 2025
$5.0M
Dysfunction of retinal neurons and circuits early in diabetic retinopathyR01EY023290 · NEI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI SOHN, JEONG-HYEON · 2014 to 2018
$1.8M
Pathology of Aging Research NetworkR24AG047115 · NIA · UNIVERSITY OF WASHINGTON · PI LADIGES, WARREN C · 2014 to 2016
$1.1M
NEI NIH HHS R01 EY023290NIA NIH HHS P01 AG001751NIA NIH HHS P30 AG013319NIA NIH HHS P30 AG024824NIA NIH HHS R01 AG019899NIA NIH HHS R24 AG047115NIA NIH HHS T32 AG000057NIA NIH HHS U01 AG022303NIA NIH HHS U01 AG022307NIA NIH HHS U19 AG023122
6 · The paper itself

Abstract

Over the past decade, a large number of discoveries have shown that interventions (genetic, pharmacological, and nutritional) increase the lifespan of invertebrates and laboratory rodents. Therefore, the possibility of developing antiaging interventions for humans has gone from a dream to a reality. However, it has also become apparent that we need more information than just lifespan to evaluate the translational potential of any proposed antiaging intervention to humans. Information is needed on how an intervention alters the "healthspan" of an animal, that is, how the physiological functions that change with age are altered. In this report, we describe the utility and the limitations of assays in mice currently available for measuring a wide range of physiological functions that potentially impact quality of life. We encourage investigators and reviewers alike to expect at minimum an overall assessment of health in several domains across several ages before an intervention is labeled as "increasing healthspan." In addition, it is important that investigators indicate any tests in which the treated group did worse or did not differ statistically from controls because overall health is a complex phenotype, and no intervention discovered to date improves every aspect of health. Finally, we strongly recommend that functional measurements be performed in both males and females so that sex differences in the rate of functional decline in different domains are taken into consideration.

Indexed as

AgingAnimalsFemaleHumansLongevityMaleMiceModels, AnimalQuality of LifeSex FactorsTranslational Research, BiomedicalAge.HealthspanLifespanPhysiological function

Identifiers

PMID26297941
PMCPMC4834833
OpenAlexW1960796618

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.