Evidence map›Paper›PMID 34713968›Full record

ArticleAging cell2021

Reevaluation of the effect of dietary restriction on different recombinant inbred lines of male and female mice.

Archana Unnikrishnan, Stephanie Matyi, Karla Garrett, Michelle Ranjo-Bishop, David B Allison, Keisuke Ejima, Xiwei Chen, Stephanie Dickinson, Arlan Richardson

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Aging cell, 2021. 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 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 17% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Integrative Omics Reveal Female-Specific Benefits of p16Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  6. Genetic regulation of fasting-induced longevity effects.bioRxiv : the preprint server for biology · 2025
    Article
  7. Article
  8. Article
  9. Article
  10. Quantifying the Impact of Co-Housing on Murine Aging Studies.bioRxiv : the preprint server for biology · 2024
    Article
  11. Quantification of healthspan in aging mice: Introducing FAMY and GRAIL.bioRxiv : the preprint server for biology · 2024
    Article
  12. Review
  13. Article
  14. Estimating Genetic Variance in Life-Span Response to Diet: Insights From Statistical Simulation.The journals of gerontology. Series A, Biological sciences and medical sciences · 2023
    Article
  15. Review
  16. Amino Acid Availability Is Not Essential for Life-Span Extension by Dietary Restriction in the Fly.The journals of gerontology. Series A, Biological sciences and medical sciences · 2022
    Article
  17. Article
  18. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 1 country.

Archana UnnikrishnanDepartment of Biochemistry & Molecular Biology, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma, USA.ORCID 0000-0001-6466-9916
Stephanie MatyiDepartment of Biochemistry & Molecular Biology, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma, USA.
Karla GarrettDepartment of Biochemistry & Molecular Biology, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma, USA.
Michelle Ranjo-BishopDepartment of Biochemistry & Molecular Biology, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma, USA.
David B AllisonDepartment of Epidemiology & Biostatistics, School of Public Health-Bloomington, Indiana University, Bloomington, Indiana, USA.
Keisuke EjimaDepartment of Epidemiology & Biostatistics, School of Public Health-Bloomington, Indiana University, Bloomington, Indiana, USA.
Xiwei ChenDepartment of Epidemiology & Biostatistics, School of Public Health-Bloomington, Indiana University, Bloomington, Indiana, USA.
Stephanie DickinsonDepartment of Epidemiology & Biostatistics, School of Public Health-Bloomington, Indiana University, Bloomington, Indiana, USA.
Arlan RichardsonDepartment of Biochemistry & Molecular Biology, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma, USA.ORCID 0000-0001-9622-7311
Indiana University Bloomington · USUniversity of Oklahoma Health Sciences Center · USOklahoma City VA Medical Center · US

Funding

Targeted DNA Methylation and Mitochondrial Heteroplasmy CoreP30AG050911 · NIA · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI HOLLY VAN REMMEN · 2015 to 2026
$13.9M
Sex hormones and arthritis in a long lived animal modelP30AG050886 · NIA · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI DAVID B ALLISON · 2015 to 2026
$11.3M
Nathan Shock Centers Coordinating CenterU24AG056053 · NIA · AMERICAN FEDERATION FOR AGING RESEARCH · PI STEVEN N. AUSTAD, Stephanie Lederman · 2017 to 2026
$6.1M
Interaction of Genotype and Level of Dietary Restriction on Lifespan and AgingR01AG045693 · NIA · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI RICHARDSON, ARLAN G. · 2014 to 2018
$3.7M
Role of DNA Methylation in Dietary Restriction mediated insulin sensitivityK01AG056655 · NIA · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI UNNIKRISHNAN, ARCHANA · 2018 to 2022
$653k
BLR&D Research Career Scientist Award ApplicationIK6BX005238 · VA · OKLAHOMA CITY VA MEDICAL CENTER · PI ARLAN G. RICHARDSON · 2020 to 2026
–
BLRD VA IK6 BX005238National Institute of Health K01AG056655-01A1National Institute of Health P30AG050886National Institute of Health P30AG050911National Institute of Health R01AG045693National Institute of Health U24AG056053NIA NIH HHS K01 AG056655NIA NIH HHS P30 AG050886NIA NIH HHS P30 AG050911NIA NIH HHS R01 AG045693NIA NIH HHS U24 AG056053
6 · The paper itself

Abstract

Dietary restriction (DR) was reported to either have no effect or reduce the lifespan of the majority of the 41-recombinant inbred (RI) lines studied by Liao et al. (Aging Cell, 2010, 9, 92). In an appropriately power longevity study (n > 30 mice/group), we measured the lifespan of the four RI lines (115-RI, 97-RI, 98-RI, and 107-RI) that were reported to have the greatest decrease in lifespan when fed 40% DR. DR increased the median lifespan of female RI-115, 97-RI, and 107-RI mice and male 115-RI mice. DR had little effect (<4%) on the median lifespan of female and male 98-RI mice and male 97-RI mice and reduced the lifespan of male 107-RI mice over 20%. While our study was unable to replicate the effect of DR on the lifespan of the RI mice (except male 107-RI mice) reported by Liao et al. (Aging Cell, 2010, 9, 92), we found that the genotype of a mouse had a major impact on the effect of DR on lifespan, with the effect of DR ranging from a 50% increase to a 22% decrease in median lifespan. No correlation was observed between the changes in either body composition or glucose tolerance induced by DR and the changes observed in lifespan of the four RI lines of male and female mice. These four RI lines of mice give the research community a unique resource where investigators for the first time can study the anti-aging mechanism of DR by comparing mice in which DR increases lifespan to mice where DR has either no effect or reduces lifespan.

Indexed as

GenotypeRecombination, GeneticAgingAnimalsBody CompositionDiet TherapyFemaleGlucose Tolerance TestKaplan-Meier EstimateLongevityMaleMiceMice, Inbred Strainsadipositydietary restrictionglucose tolerancelifespanrecombinant inbred lines

Identifiers

PMID34713968
PMCPMC8590105
OpenAlexW3210300318

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.