Evidence mapPaperPMID 41560403Full record

ArticleJournal of cachexia, sarcopenia and muscle2026

Associations Between Growth Differentiating Factor-15 and Frailty in Older Adults From the MAPT Study.

Juan Luis Sánchez-Sánchez, Yves Rolland, Alexandre Lucas, Sophie Guyonnet, Bruno Vellas, Philipe de Souto Barreto, MAPT/DSA Group

Abstract read
In one paragraph

Article in Journal of cachexia, sarcopenia and muscle, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

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

  1. Pooled it
  2. 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

7 authors.

Juan Luis Sánchez-SánchezIHU HealthAge, Toulouse, France.ORCID https://orcid.org/0000-0002-2507-6015
Yves RollandIHU HealthAge, Toulouse, France.
Alexandre LucasInstitut National de la Santé et de la Recherche Médicale (INSERM), UMR 1297, Institute of Metabolic and Cardiovascular Diseases, Toulouse, France.
Sophie GuyonnetIHU HealthAge, Toulouse, France.
Bruno VellasIHU HealthAge, Toulouse, France.
Philipe de Souto BarretoIHU HealthAge, Toulouse, France.
MAPT/DSA Group

Funding

Agence Nationale de la Recherche ANR-23-IAHU-0011Alzheimer Prevention in Occitania and Catalonia (APOC Chair of Excellence-Inspire Program)Association Monegasque pour la Recherche sur la maladie d'AlzheimerAvid Radiopharmaceuticals Inc.European Regional Development Fund MP0022856ExonHit Therapeutics SAFrench Ministry of Health PHRC 2008French Ministry of Health PHRC 2009Gérontopôle of ToulouseINSERM-University of Toulouse III UMR 1295 UnitPierre Fabre Research InstituteRegion Occitanie/Pyrénées-Méditerranée 1901175
6 · The paper itself

Abstract

backgroundFrailty is a prevalent syndrome in older adults and is associated with increased vulnerability to adverse health outcomes. Growth differentiation factor 15 (GDF-15), a cytokine involved in mitochondrial dysfunction and inflammation, has been proposed as a potential biomarker for age-related conditions. Evidence on the association between GDF-15 and frailty in older adults is limited. This study explores the relationship between plasma GDF-15 levels and frailty onset in community-dwelling older adults.

methodsA secondary analysis was performed on 1096 participants (mean age = 75.2 ± 4.5 years; 64.5% women) from the Multidomain Alzheimer Prevention Trial (MAPT). Plasma GDF-15 levels were measured at year 1. Frailty was assessed using the Fried phenotype. Logistic regression was used to examine cross-sectional associations between GDF-15 and frailty, while mixed effects logistic regression or Cox proportional hazards models assessed longitudinal associations over a 4-year follow-up.

resultsHigher plasma GDF-15 levels (both as continuous and categorical) were cross-sectionally associated with frailty (high vs. low GDF-15: OR = 3.56, 95% CI = 1.58-8.03). Longitudinally, very high GDF-15 levels predicted an increased risk of incident frailty (HR = 1.69, 95% CI = 1.03-2.78).

conclusionsElevated plasma GDF-15 levels were associated with frailty in older adults, suggesting its potential as a biomarker for increased vulnerability and an indicator of increased risk over time. Our results support a pleiotropic role of GDF-15, with low physiological levels not contributing to frailty development.

Indexed as

FrailtyGrowth Differentiation Factor 15AgedAged, 80 and overBiomarkersCross-Sectional StudiesFemaleFrail ElderlyHumansMaleBiomarkersGDF15 protein, humanGrowth Differentiation Factor 15ageingbiomarkersfrailtygrowth differentiation factor 15

Identifiers

PMID41560403
PMCPMC12820345

What Socratic holds

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Registered trials

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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.