Evidence map›Paper›PMID 39353910›Full record

ArticleTranslational psychiatry2024

Association between probable sarcopenia and dementia risk: a prospective cohort study with mediation analysis.

Yitong Ling, Shiqi Yuan, Xiaxuan Huang, Shanyuan Tan, Hongtao Cheng, Li Li, Shuna Li, Liying Huang, Anding Xu, Jun Lyu

Abstract read
In one paragraph

Article in Translational psychiatry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

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

  1. Pooled it
  2. The crossroads between osteosarcopenia and intrinsic capacity-a narrative review.The journals of gerontology. Series A, Biological sciences and medical sciences · 2026
    Review
  3. Article
  4. 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

10 authors.

Yitong Ling *Department of Neurology, Jinan University First Affiliated Hospital, Guangzhou, Guangdong, China.
Shiqi Yuan *Department of Neurology, Jinan University First Affiliated Hospital, Guangzhou, Guangdong, China.ORCID 0000-0002-2794-2546
Xiaxuan Huang *Department of Neurology, Jinan University First Affiliated Hospital, Guangzhou, Guangdong, China.
Shanyuan TanDepartment of Neurology, Jinan University First Affiliated Hospital, Guangzhou, Guangdong, China.
Hongtao ChengSchool of Nursing, Jinan University, Guangzhou, Guangdong, China.
Li LiDepartment of Clinical Research, Jinan University First Affiliated Hospital, Guangzhou, Guangdong, China.
Shuna LiDepartment of Clinical Research, Jinan University First Affiliated Hospital, Guangzhou, Guangdong, China.
Liying HuangDepartment of Clinical Research, Jinan University First Affiliated Hospital, Guangzhou, Guangdong, China.
Anding XuDepartment of Neurology, Jinan University First Affiliated Hospital, Guangzhou, Guangdong, China. tlil@jnu.edu.cn.
Jun LyuDepartment of Clinical Research, Jinan University First Affiliated Hospital, Guangzhou, Guangdong, China. lyujun2020@jnu.edu.cn.ORCID 0000-0002-2237-8771

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The role of alcohol consumption as a mediator in the risk between sarcopenia and dementia remains inadequately studied. There is currently limited research on whether the association between sarcopenia and the risk of Alzheimer's disease (AD) is influenced by genetic susceptibility. Our study incorporated a total of 483,637 baseline non-dementia participants, who were classified into groups of individuals with no sarcopenia and those with probable sarcopenia based on the definition. We employed Cox proportional hazards models to evaluate the association between probable sarcopenia and the risk of all cause dementia (ACD), AD, and vascular dementia (VD). We conducted mediation analysis to explore the role of alcohol consumption in the association between probable sarcopenia and the risk of ACD, AD, and VD. During the median follow-up period of 13.6 years, we documented 9000 new cases of ACD (including 4061 AD and 2025 VD). Fully adjusted multivariate model revealed a significant correlation between probable sarcopenia and elevated risk for ACD (HR = 1.54, 95% CI: 1.46-1.62, p < 0.001), AD (HR = 1.32, 95% CI: 1.21-1.43, p < 0.001), and VD (HR = 1.69, 95% CI: 1.52-1.89, p < 0.001). Mediation analysis elucidates that alcohol consumption explained 12.8%, 15.2%, and 11.1% of the associations of probable sarcopenia with the risk of ACD, AD, and VD, respectively. An interactive relationship prevails between probable sarcopenia and genetic factors (p for interaction <0.001), and regardless of the degree of genetic risk, probable sarcopenia correlates with an elevated AD risk. Our study reveals a significant association between probable sarcopenia and an increased risk of dementia, with alcohol consumption playing a mediating role in this association. There is an interaction between probable sarcopenia and genetic susceptibility related to the risk of AD.

Indexed as

Alcohol DrinkingDementiaMediation AnalysisSarcopeniaAgedAged, 80 and overAlzheimer DiseaseDementia, VascularFemaleGenetic Predisposition to DiseaseHumansMaleMiddle AgedProportional Hazards ModelsProspective StudiesRisk Factors

Identifiers

PMID39353910
PMCPMC11445531

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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.