Evidence map›Paper›PMID 41174599›Full record

Observational studyBMC oral health2025

Oral-Sarcopenia nexus in health disparities: chewing and blood mediated pathways in a Chinese aging cohort.

Yong Xiang, Guosong Wang, Yiting Cheng, Yuhan Zhang, Jialiang Zhao, Birong Dong, He Cai, Li Cheng, Tao Hu

Abstract readObservational Study
In one paragraph

Observational study in BMC oral health, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

9 authors.

Yong Xiang *State Key Laboratory of Oral Diseases & National Center for Stomatology & National Clinical Research Center for Oral Diseases & Frontier Innovation Center for Dental Medicine Plus, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
Guosong Wang *State Key Laboratory of Oral Diseases & National Center for Stomatology & National Clinical Research Center for Oral Diseases & Frontier Innovation Center for Dental Medicine Plus, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
Yiting ChengState Key Laboratory of Oral Diseases & National Center for Stomatology & National Clinical Research Center for Oral Diseases & Frontier Innovation Center for Dental Medicine Plus, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
Yuhan ZhangState Key Laboratory of Oral Diseases & National Center for Stomatology & National Clinical Research Center for Oral Diseases & Frontier Innovation Center for Dental Medicine Plus, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
Jialiang ZhaoState Key Laboratory of Oral Diseases & National Center for Stomatology & National Clinical Research Center for Oral Diseases & Frontier Innovation Center for Dental Medicine Plus, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
Birong DongWest China Hospital, National Clinical Research Center for Geriatrics, Sichuan University, Chengdu, China.
He CaiState Key Laboratory of Oral Diseases & National Center for Stomatology & National Clinical Research Center for Oral Diseases & Frontier Innovation Center for Dental Medicine Plus, West China Hospital of Stomatology, Sichuan University, Chengdu, China. caihe.dr@scu.edu.cn.
Li ChengState Key Laboratory of Oral Diseases & National Center for Stomatology & National Clinical Research Center for Oral Diseases & Frontier Innovation Center for Dental Medicine Plus, West China Hospital of Stomatology, Sichuan University, Chengdu, China. dentistcl@scu.edu.cn.
Tao HuState Key Laboratory of Oral Diseases & National Center for Stomatology & National Clinical Research Center for Oral Diseases & Frontier Innovation Center for Dental Medicine Plus, West China Hospital of Stomatology, Sichuan University, Chengdu, China. hutao@scu.edu.cn.

Funding

National Key Research and Development Program of China 2023YFC3605600National Natural Science Foundation of China 72104162Research and Development Program, West China Hospital of Stomatology Sichuan University LCYJ-ZD-202301
6 · The paper itself

Abstract

backgroundAging affects oral health and skeletal muscle, but the associations between oral diseases and possible sarcopenia remain understudied, especially in low-income regions. Thus, the study aimed to explore this relationship and potential mediating pathways.

methodsData were from the 2021-2022 follow-up of the West China Health and Aging Trend study. Assessments included questionnaires, oral examinations, muscle strength tests, physical performance tests, and routine blood tests. Logistic regression analyses, subgroup analyses, and mediation analyses were conducted.

resultsA total of 532 participants aged ≥ 60 years were included, with a possible sarcopenia prevalence of 50.4%. After adjusting for confounders, those with decayed and filled roots (DFRoot) had a 46% higher risk of possible sarcopenia than those without DFRoot, while those with a number of remaining natural teeth (NRT) ≥ 20 had a 53% lower risk. Participants with number of functional tooth loss (NFTL) > 16 had an 83% higher risk of possible sarcopenia than those with ≤ 16. Mediation analyses indicated that impaired chewing ability, systemic inflammation, and impaired liver function partially explain the oral-sarcopenia nexus. Subgroup analyses showed significant associations between NRT ≥ 20 (OR 0.49, 95% CI 0.27 to 0.89), NFTL > 16 (1.90, 1.05 to 3.43), and possible sarcopenia in adults aged ≥ 70 years.

conclusionsOral health emerged as a modifiable risk factor for sarcopenia in vulnerable older adults, with chewing impairment, systemic inflammation, and liver dysfunction partly explaining this association. These findings support integrating oral healthcare into sarcopenia prevention strategies, particularly in resource-limited settings. However, given the cross-sectional design, causal interpretations remain limited, and the identified mediation analyses should be viewed as associative rather than causal. Further longitudinal investigations are warranted to confirm these mechanisms and to evaluate whether oral health interventions can effectively reduce sarcopenia risk.

trial registrationChiCTR1800018895.

Indexed as

AgingHealth Status DisparitiesMasticationMouth DiseasesOral HealthSarcopeniaAgedChinaCohort StudiesEast Asian PeopleFemaleHumansMaleMiddle AgedMuscle StrengthPrevalenceAgingMediating effectOral diseasesPublic healthSarcopenia

Identifiers

PMID41174599
PMCPMC12577094

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.