Edentulism as an Independent Risk Factor for Sarcopenia: Evidence from Cross-sectional and Longitudinal Analyses Based on the CHARLS Cohort

Abstract Background Edentulism and sarcopenia are two highly prevalent, age-related conditions that share common nutritional, inflammatory, and functional pathways. Whether tooth loss independently contributes to the development of sarcopenia—and in which population strata this effect is strongest—remains uncertain, especially in Asian cohorts. Methods We analysed 17,099 participants (baseline 2011) from the China Health and Retirement Longitudinal Study (CHARLS). Sarcopenia was defined by Asian Working Group for Sarcopenia 2019 criteria. Multivariable logistic models (wave 1 cross-sectional) and Cox models (waves 1–3 longitudinal, seven-year follow-up) were fitted sequentially: Model 1 (crude), Model 2 (plus demographic covariates), Model 3 (plus metabolic/ inflammatory factors). Propensity-score matching (PSM) was applied to minimise selection bias. Subgroup analyses covered sex, residence, marital status, education, smoking, drinking, and region. Sensitivity analyses tested robustness. Results Edentulism prevalence was 8.8%; sarcopenia prevalence, 15.0%. Cross-sectionally, edentulism increased sarcopenia risk in Model 1 (β = 1.359, P  < 0.001) and remained significant after full adjustment (β = 0.271, P  = 0.023). In the PSM set, the effect strengthened (Model 3 β = 0.453, P  = 0.004). Longitudinally, edentulism predicted incident sarcopenia (Model 1 β = 1.109, P  < 0.001); significance attenuated after full adjustment (β = 0.070, P  = 0.221) but re-emerged in PSM analyses (β = 0.193, P  = 0.008). Subgroup analyses showed consistently higher risks in males, rural residents, low-education groups, non-smokers, non-drinkers, and western regions. Conclusions Edentulism is a robust, independent marker of elevated sarcopenia risk in Chinese adults, with particularly strong effects in socio-economically vulnerable subgroups. Routine oral-health screening should be integrated into geriatric assessments to identify patients at high risk for sarcopenia.