Evidence map›Paper›PMID 39447036›Full record

ArticleThe journals of gerontology. Series A, Biological sciences and medical sciences2025

The Influence of Body Mass Index on Biomarkers of Cellular Senescence in Older Adults.

Allyson K Palmer, Jennifer St Sauver, Roger A Fielding, Elizabeth Atkinson, Thomas A White, Michaela McGree, Susan Weston, Nathan K LeBrasseur

Abstract read
In one paragraph

Article in The journals of gerontology. Series A, Biological sciences and medical sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Human Adipose Tissue Metabolism in Obesity.Journal of obesity & metabolic syndrome · 2025
    Review
  5. 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

8 authors.

Allyson K PalmerRobert and Arlene Kogod Center on Aging, Mayo Clinic, College of Medicine, Rochester, Minnesota, USA.
Jennifer St SauverDepartment of Quantitative Health Sciences, Mayo Clinic, Rochester, Minnesota, USA.
Roger A FieldingNutrition, Exercise Physiology and Sarcopenia Laboratory, Jean Mayer USDA Human Nutrition Research Center on Aging, Tufts University, Boston, Massachusetts, USA.
Elizabeth AtkinsonDepartment of Quantitative Health Sciences, Mayo Clinic, Rochester, Minnesota, USA.ORCID 0000-0002-1191-3775
Thomas A WhiteRobert and Arlene Kogod Center on Aging, Mayo Clinic, College of Medicine, Rochester, Minnesota, USA.
Michaela McGreeDepartment of Quantitative Health Sciences, Mayo Clinic, Rochester, Minnesota, USA.
Susan WestonDepartment of Quantitative Health Sciences, Mayo Clinic, Rochester, Minnesota, USA.
Nathan K LeBrasseurRobert and Arlene Kogod Center on Aging, Mayo Clinic, College of Medicine, Rochester, Minnesota, USA.

Funding

TUFTS--FIELDINGP30AG031679 · NIA · BRIGHAM AND WOMEN'S HOSPITAL · PI LEWIS LIPSITZ · 2008 to 2026
$23.9M
Senescence and Growth Differentiation Factors as Modifiers of AgingR01AG055529 · NIA · MAYO CLINIC ROCHESTER · PI LEBRASSEUR, NATHAN K · 2018 to 2022
$3.1M
Interdisciplinary Infrastructure for Aging Research: Rochester Epidemiology ProjectR33AG058738 · NIA · MAYO CLINIC ROCHESTER · PI LEBRASSEUR, NATHAN K, OLSON, JANET E · 2020 to 2022
$2.4M
Phenotypes of Aging & SenescenceR56AG060907 · NIA · CALIFORNIA PACIFIC MED CTR RES INSTITUTE · PI CUMMINGS, STEVEN RON, LEBRASSEUR, NATHAN K · 2018 to 2018
$684k
American Federation for Aging ResearchGlenn Foundation for Medical ResearchMayo Clinic Research CommitteeNIA NIH HHS P30 AG031679NIA NIH HHS R01 AG055529NIA NIH HHS R33 AG058738NIA NIH HHS R56 AG060907NIH Boston Claude D. Pepper Center 1P30AG031679Robert and Arlene Kogod Center on Aging Kogod Scholar Awardthe US Department of Agriculture 58-8050-9-004
6 · The paper itself

Abstract

Obesity accelerates the onset and progression of age-related conditions. In preclinical models, obesity drives cellular senescence, a cell fate that compromises tissue health and function, in part through a robust and diverse secretome. In humans, components of the secretome have been used as senescence biomarkers that are predictive of age-related disease, disability, and mortality. Here, using biospecimens and clinical data from two large and independent cohorts of older adults, we tested the hypothesis that the circulating concentrations of senescence biomarkers are influenced by body mass index. After adjusting for age, sex, and race, we observed significant increases in activin A, Fas, MDC, PAI1, PARC, TNFR1, and VEGFA, and a significant decrease in RAGE, from normal weight, to overweight, to obesity body mass index categories by linear regression in both cohorts (all p < .05). These results highlight the influence of body mass index on circulating concentrations of senescence biomarkers.

Indexed as

AgingBiomarkersBody Mass IndexCellular SenescenceObesityAgedAged, 80 and overFemaleHumansMaleMiddle AgedBiomarkersBody mass indexCellular senescenceObesitySenescence-associated secretory phenotype

Identifiers

PMID39447036
PMCPMC11949428

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.