Evidence map›Paper›PMID 41351715›Full record

ArticleGeroScience2026

The frailty mortality link in people with chronic diseases pertaining to 13 body organ systems: findings from the UK Biobank study.

Justine Dastouet, Aurore Fayosse, Louis Jacob, Archana Singh-Manoux, Séverine Sabia, Benjamin Landré

Abstract read
In one paragraph

Article in GeroScience, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Justine DastouetEpidemiology of Ageing and Neurodegenerative Diseases, Université Paris Cité, INSERM U1153, CRESS, 10 Avenue de Verdun, Paris, 75010, France.
Aurore FayosseEpidemiology of Ageing and Neurodegenerative Diseases, Université Paris Cité, INSERM U1153, CRESS, 10 Avenue de Verdun, Paris, 75010, France.
Louis JacobEpidemiology of Ageing and Neurodegenerative Diseases, Université Paris Cité, INSERM U1153, CRESS, 10 Avenue de Verdun, Paris, 75010, France.
Archana Singh-ManouxEpidemiology of Ageing and Neurodegenerative Diseases, Université Paris Cité, INSERM U1153, CRESS, 10 Avenue de Verdun, Paris, 75010, France.
Séverine SabiaEpidemiology of Ageing and Neurodegenerative Diseases, Université Paris Cité, INSERM U1153, CRESS, 10 Avenue de Verdun, Paris, 75010, France.
Benjamin LandréEpidemiology of Ageing and Neurodegenerative Diseases, Université Paris Cité, INSERM U1153, CRESS, 10 Avenue de Verdun, Paris, 75010, France. benjamin.landre@u-paris.fr.ORCID http://orcid.org/0000-0002-3893-4197

Funding

Agence Nationale de la Recherche France 2030 ANR-23-PAVH-0006
6 · The paper itself

Abstract

Frailty in older adults, particularly those with chronic diseases, has a robust association with risk of mortality, but whether this is the case in middle-aged adults is unclear. We examined the frailty-mortality association in middle-aged adults with chronic diseases and multimorbidity. Data on Fried's frailty phenotype (robust, prefrail, frail) and 47 chronic diseases, mapped to 13 body organ systems, was available on 230,960 participants of the UK Biobank study (mean age 57.8, range 38.0-72.0). The mortality follow-up was 13.3 (± 2.1) years, and associations with mortality were examined using Cox regression, adjusted for socio-demographic factors and health behaviours. Compared to the robust group, frailty (HR, 2.32 (95% confidence intervals, 2.21; 2.43)) and prefrailty (1.35 (1.31; 1.39)) in those with diseases in any body organ system had a higher risk of mortality. Frailty was associated with a higher mortality risk for all 13 groups (all p < 0.01); estimates ranged from 2.25 (2.12; 2.39) for circulatory system diseases to 2.97 (2.60; 3.39) for the eye system. The same was the case for prefrailty; estimates ranged from 1.33 (1.23; 1.43) to 1.61 (1.03; 2.51). Between 19 and 34% of the mortality risk in the 13 disease groups could potentially be explained by frailty/prefrailty. Frailty (p < 0.01) and prefrailty (p < 0.01) had stronger associations with mortality in those with diseases affecting multiple organ systems. These findings highlight the importance of frailty in middle-aged adults with chronic diseases, suggesting that a third of the excess risk of mortality could potentially be addressed by improving frailty status.

Indexed as

FrailtyAdultAgedChronic DiseaseFemaleHumansMaleMiddle AgedMultimorbidityRisk FactorsUK BiobankUnited KingdomAgeingChronic diseaseFrailtyMortalityMultimorbidityUK Biobank

Identifiers

PMID41351715
PMCPMC13601399

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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 OpenQuestion graph.