Evidence map›Paper›PMID 31111669›Full record

ArticleAging cell2019

Late-life time-restricted feeding and exercise differentially alter healthspan in obesity.

Marissa J Schafer, Daniel L Mazula, Ashley K Brown, Thomas A White, Elizabeth Atkinson, Vesselina M Pearsall, Zaira Aversa, Grace C Verzosa, Leslie A Smith, Aleksey Matveyenko and 2 more

Abstract read
In one paragraph

Article in Aging cell, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

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

  1. Pooled it
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  10. Obesity, Senescence, and Senolytics.Handbook of experimental pharmacology · 2022
    Article
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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

12 authors.

Marissa J SchaferRobert and Arlene Kogod Center on Aging, Mayo Clinic, Rochester, Minnesota.
Daniel L MazulaRobert and Arlene Kogod Center on Aging, Mayo Clinic, Rochester, Minnesota.
Ashley K BrownRobert and Arlene Kogod Center on Aging, Mayo Clinic, Rochester, Minnesota.
Thomas A WhiteRobert and Arlene Kogod Center on Aging, Mayo Clinic, Rochester, Minnesota.
Elizabeth AtkinsonDivision of Biomedical Statistics and Informatics, Department of Health Sciences Research, Mayo Clinic, Rochester, Minnesota.
Vesselina M PearsallRobert and Arlene Kogod Center on Aging, Mayo Clinic, Rochester, Minnesota.
Zaira AversaRobert and Arlene Kogod Center on Aging, Mayo Clinic, Rochester, Minnesota.
Grace C VerzosaDepartment of Surgery, Mayo Clinic, Rochester, Minnesota.
Leslie A SmithDepartment of Surgery, Mayo Clinic, Rochester, Minnesota.
Aleksey MatveyenkoDepartment of Physiology and Biomedical Engineering, Mayo Clinic, Rochester, Minnesota.
Jordan D MillerRobert and Arlene Kogod Center on Aging, Mayo Clinic, Rochester, Minnesota.
Nathan K LeBrasseurRobert and Arlene Kogod Center on Aging, Mayo Clinic, Rochester, Minnesota.

Funding

Aging and Resiliency in Mice: Optimizing Assessment Protocols and Testing InterventionsR01AG053832 · NIA · MAYO CLINIC ROCHESTER · PI LEBRASSEUR, NATHAN K, MILLER, JORDAN D · 2016 to 2020
$2.0M
Role of senescent cells in the pathogenesis of Marfan-associated cardiovascular diseaseR01HL141819 · NHLBI · MAYO CLINIC ROCHESTER · PI MILLER, JORDAN D · 2018 to 2021
$1.6M
Glenn Foundation for Medical ResearchNHLBI NIH HHS R01 HL141819NIA NIH HHS R01 AG053832Robert and Arlene Kogod
6 · The paper itself

Abstract

Aging and obesity increase multimorbidity and disability risk, and determining interventions for reversing healthspan decline is a critical public health priority. Exercise and time-restricted feeding (TRF) benefit multiple health parameters when initiated in early life, but their efficacy and safety when initiated at older ages are uncertain. Here, we tested the effects of exercise versus TRF in diet-induced obese, aged mice from 20 to 24 months of age. We characterized healthspan across key domains: body composition, physical, metabolic, and cardiovascular function, activity of daily living (ADL) behavior, and pathology. We demonstrate that both exercise and TRF improved aspects of body composition. Exercise uniquely benefited physical function, and TRF uniquely benefited metabolism, ADL behavior, and circulating indicators of liver pathology. No adverse outcomes were observed in exercised mice, but in contrast, lean mass and cardiovascular maladaptations were observed following TRF. Through a composite index of benefits and risks, we conclude the net healthspan benefits afforded by exercise are more favorable than those of TRF. Extrapolating to obese older adults, exercise is a safe and effective option for healthspan improvement, but additional comprehensive studies are warranted before recommending TRF.

Indexed as

AgingAnimal FeedFastingPhysical Conditioning, AnimalAnimalsMaleMiceMice, Inbred C57BLObesityagingexercisehealthspanobesityphysical activitytime-restricted feeding

Identifiers

PMID31111669
PMCPMC6612646

What OpenQuestion holds

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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.