OSCR

Effects of Sarcopenia and Frailty on Cognitive Function, Brain Volume, and Dementia Risk: A Prospective Cohort Study Based on UK Biobank.

A correction to this paper has been published: the notice, 42564477, from Europe PMC.

Overview

  1. Division of Biostatistics, Department of Biomedical Systems Informatics, Yonsei University College of Medicine, Seoul, Korea
  2. Department of Neurology, Yonsei University College of Medicine, Seoul, Korea
  3. Department of Neurology, Yongin Severance Hospital, Yonsei University Health System, Yongin, Korea
  4. Yonsei Beyond Lab, Yongin, Korea
Institutions: Yonsei University (South Korea); Yonsei University Health System (South Korea); Yongin Severance Hospital (South Korea)
Journal: Dementia and neurocognitive disorders, volume 25, issue 2, pages 115-129
Dates: received 15 March 2026; accepted 9 April 2026; published online 15 April 2026; in print April 2026
Type: Research article · Language: English
License: CC BY-NC
Identifiers: DOI 10.12779/dnd.2026.25.2.115 · PMID 42088088 · PMCID PMC13136627 · OpenAlex W7159617876
Open access: diamond, a free copy (OpenAlex)
Status: data only
Categories: structural MRI / diffusion (modality), human (organism), Alzheimer's / dementia (population), cognitive (subfield)
Methods: Statistics
Keywords: Sarcopenia, Frailty, Cognitive Function, Brain Atrophy, Dementia
Topic: Nutrition and Health in Aging (Physiology, Medicine), according to OpenAlex
Funding: Yonsei University College of Medicine (6-2023-0145); Yongin Severance Hospital, Yonsei University College of Medicine (Z-2023-0004)
Citations: not cited yet (Europe PMC); 47 references in the paper
Notices: A correction to this paper has been published (42564477, from Europe PMC)

Abstract

Background and Purpose: Despite the rising prevalence of sarcopenia, frailty, and dementia, their interrelationships remain unclear. This study investigated the associations of sarcopenia and frailty with cognitive function, brain structure, incident dementia, and their longitudinal changes.

Methods: This study included 390,903 participants aged 40–70 years from the UK Biobank. Sarcopenia was assessed using hand grip strength, muscle mass index, and gait speed; frailty was measured based on weight loss, exhaustion, physical activity, gait speed, and grip strength. Outcomes included cognitive test scores, magnetic resonance imaging-derived brain volumes, and incident dementia. Linear regression, Cox proportional hazards models, and linear mixed effects models were used.

Results: Frailty was associated with poorer performance across cognitive domains (all p<0.05), while sarcopenia was associated with slower reaction time (p<0.001). Frailty, but not sarcopenia, was associated with reduced cortical volume. Both conditions increased all-cause dementia risk: frailty with a dose-response gradient (hazard ratio [HR], 2.11; 95% confidence interval [CI], 1.87 to 2.38) and particularly strong associations with vascular dementia (VaD, HR, 2.39; 95% CI, 1.85 to 3.07); sarcopenia with a moderate increase (HR, 1.53; 95% CI, 1.09 to 2.12). Longitudinally, sarcopenia—but not frailty—was associated with accelerated cognitive decline.

Conclusions: Sarcopenia and frailty show overlapping but non-identical patterns of association with neurocognitive outcomes: sarcopenia was linked to longitudinal cognitive decline, whereas frailty was associated with cortical volume reduction and VaD. Early identification of these conditions is crucial for mitigating neurodegenerative decline and reducing dementia risk.

Reproduced under the paper's license (CC BY-NC), from the paper cited above.

Code

The paper links to its data, not to its authors' code: see the Data section.

Tracing map

A tracing map links a paper to the code its authors published: this paper has none, so it has no map.

Data

Datasets cited

Versions

The history of this record: each version stored by the harvester or made by a correction of its authors or of the maintainers of its code, and what changed in its facts. The texts of the paper (its abstract, its availability statements) are not part of it; versions that changed only those are not listed.

Version 1, 29 September 2026: the first record

Recorded: type, language, journal, volume, issue, pages, dates, 2 authors, 5 keywords, 2 funders, 43 references, 1 integrity notice.

Cite

This paper

Heo, S.-J., & Chun, M. Y. (2026). Effects of Sarcopenia and Frailty on Cognitive Function, Brain Volume, and Dementia Risk: A Prospective Cohort Study Based on UK Biobank. Dementia and neurocognitive disorders, 25(2), 115-129. https://doi.org/10.12779/dnd.2026.25.2.115

BibTeX

@article{heo2026effects,
author = {Heo, Seok-Jae and Chun, Min Young},
title = {{Effects of Sarcopenia and Frailty on Cognitive Function, Brain Volume, and Dementia Risk: A Prospective Cohort Study Based on UK Biobank}},
journal = {Dementia and neurocognitive disorders},
year = {2026},
month = apr,
volume = {25},
number = {2},
pages = {115--129},
publisher = {Korean Dementia Association},
issn = {1738-1495},
doi = {10.12779/dnd.2026.25.2.115},
url = {https://doi.org/10.12779/dnd.2026.25.2.115},
pmid = {42088088},
pmcid = {PMC13136627}
}

RIS

TY - JOUR
AU - Heo, Seok-Jae
AU - Chun, Min Young
TI - Effects of Sarcopenia and Frailty on Cognitive Function, Brain Volume, and Dementia Risk: A Prospective Cohort Study Based on UK Biobank
T2 - Dementia and neurocognitive disorders
J2 - Dement Neurocogn Disord
PY - 2026
DA - 2026/04/15
VL - 25
IS - 2
SP - 115
EP - 129
SN - 1738-1495
PB - Korean Dementia Association
DO - 10.12779/dnd.2026.25.2.115
UR - https://doi.org/10.12779/dnd.2026.25.2.115
LA - en
ER -

CSL-JSON

{
"id": "10.12779/dnd.2026.25.2.115",
"type": "article-journal",
"title": "Effects of Sarcopenia and Frailty on Cognitive Function, Brain Volume, and Dementia Risk: A Prospective Cohort Study Based on UK Biobank",
"container-title": "Dementia and neurocognitive disorders",
"author": [
{
"family": "Heo",
"given": "Seok-Jae"
},
{
"family": "Chun",
"given": "Min Young"
}
],
"container-title-short": "Dement Neurocogn Disord",
"volume": "25",
"issue": "2",
"page": "115-129",
"DOI": "10.12779/dnd.2026.25.2.115",
"PMID": "42088088",
"PMCID": "PMC13136627",
"ISSN": "1738-1495",
"publisher": "Korean Dementia Association",
"URL": "https://doi.org/10.12779/dnd.2026.25.2.115",
"language": "en",
"issued": {
"date-parts": [
[
2026,
4,
15
]
]
}
}

Similar papers

The papers with a page that share the most with this one: the tools found in their code, their categories, datasets, cited references and authors, the rarest counting most.

[1] doi:10.1093/brain/awaf307
Brain signatures of nociplastic pain: Fibromyalgia Index and descending modulation at population level.
Journal: Brain : a journal of neurology
In common: ukbiobank.ac.uk/enable-your-research/apply-for-access, structural MRI / diffusion, 3 references
[2] doi:10.7554/elife.108109 [code]
Multimodal MRI marker of cognition explains the association between cognition and mental health in the UK Biobank.
Journal: eLife
In common: ukbiobank.ac.uk/enable-your-research/apply-for-access, structural MRI / diffusion, cognitive, 2 references
[3] doi:10.1186/s40708-026-00316-y [code]
Generalizable and explainable deep learning for brain MRI: a multi-cohort evaluation of 3D architectures for age and sex prediction.
Journal: Brain informatics
In common: ukbiobank.ac.uk/enable-your-research/apply-for-access, structural MRI / diffusion, 2 references
[4] doi:10.1038/s44220-026-00680-y [code]
The neuroimaging correlates of depression established across six large-scale population datasets.
Journal: Nature. Mental health
In common: ukbiobank.ac.uk/enable-your-research/apply-for-access, 2 references
[5] doi:10.1093/cercor/bhag105 [code]
The tangential growth of the human visual cortex and maternal smoking during pregnancy.
Journal: Cerebral cortex (New York, N.Y. : 1991)
In common: ukbiobank.ac.uk/enable-your-research/apply-for-access, 2 references
[6] doi:10.1038/s41467-026-75661-x [code]
A neural signature of sleep deprivation in the human brain.
Journal: Nature communications
In common: ukbiobank.ac.uk/enable-your-research/apply-for-access, cognitive, 1 reference
[7] doi:10.1038/s41467-026-73262-2 [code]
Robust but independent sex differences in human brain function, structure, and behavior.
Journal: Nature communications
In common: ukbiobank.ac.uk/enable-your-research/apply-for-access, structural MRI / diffusion, 1 reference
[8] doi:10.1038/s41467-026-71738-9 [code]
Genetic landscape of adult executive function reveals a cell-type-specific developmental origin.
Journal: Nature communications
In common: ukbiobank.ac.uk/enable-your-research/apply-for-access, cognitive, 1 reference
[9] doi:10.1038/s41467-026-76676-0 [code]
Determinants of functional burden pleiotropy and gene dosage responses across human traits.
Journal: Nature communications
In common: ukbiobank.ac.uk/enable-your-research/apply-for-access, 1 reference
[10] doi:10.1126/sciadv.adu9309 [code]
Variations of global brain asymmetry are associated with aging and related diseases.
Journal: Science advances
In common: Alzheimer's / dementia, cognitive, 3 references

Contribute

The authors of this paper can claim it, correct its record and validate its tracing map, and the maintainers of its code (its owner, or a public member of its organization) correct what it says of their repository; anyone signed in can ask for its removal. Every request goes to OSCR's own machine, which answers it; your account page follows them.

Sign in with ORCID to claim this paper as one of its authors, correct its record or validate its tracing map: when the paper's metadata lists your ORCID iD, you are recognized at once. Maintainers of its code: sign in with GitHub, then claim the repository on your account page.

Request its removal

To ask OSCR to remove this record, the copies of its authors' scripts or its tracing map, use the removal request page: signed in, you say who you are, what to remove and why, then review and confirm the request. Published rules decide every request (how).

Discussion, reproductions, activity

Discussion: questions and error reports about this paper and its code, from signed-in readers and its authors. It opens with sign-in.

Reproductions: reports from readers who ran the authors' code: what they reproduced, with which environment, commit and data. It opens with sign-in.

Activity: what happens around this paper: new versions of its record, its map's validation, discussions and reproductions. It opens with sign-in.