{"title":"Association of body composition with all-cause mortality among U.S. adults with osteoporosis or osteopenia: a population-based study.","authors":"Keju Wang, Xuefei Li, Hao Wan, Peng Tian, Chang Lu, Xiaotong Zhang, Xiaolin Ding","doi":"10.1007/s42000-026-00825-9","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Adults with osteopenia or osteoporosis have increased risks of adverse outcomes; however, mortality risk varies substantially and may be influenced by body composition. Evidence for the joint impact of low muscle mass and percentage-based adiposity in this population remains limited.</p><p><strong>Objectives: </strong>To examine the independent and combined associations of low muscle mass and obesity with all-cause mortality among U.S. adults with osteopenia or osteoporosis and to characterize the dose-response relationship between total fat mass and mortality.</p><p><strong>Methods: </strong>We performed a retrospective cohort analysis of NHANES cycles with concurrent whole-body DXA (appendicular lean mass and total fat mass) and site-specific BMD assessments (1999-2006, 2013-2014, and 2017-2018). Eligible participants with osteopenia or osteoporosis and mortality linkage were included (unweighted n = 3,918). Low muscle mass (LMM) was defined by DXA-derived appendicular lean mass index (ALMI; men < 7.0 kg/m², women < 5.5 kg/m²), while obesity was operationally defined by DXA body fat percentage (FM%; men > 30%, women > 42%) instead of body mass index (BMI). Survey-weighted Cox models and restricted cubic splines were utilized.</p><p><strong>Results: </strong>Over a median follow-up of 14.8 years, 1,095 deaths occurred. In fully adjusted models, low muscle mass was associated with higher mortality (HR = 1.59, 95% CI: 1.30-1.95). Jointly, both low muscle mass alone (HR = 1.70, 95% CI: 1.30-2.23) and low muscle mass with obesity (HR = 1.45, 95% CI: 1.13-1.87) were associated with higher mortality compared with the normal phenotype, whereas obesity alone was not; notably, the isolated low muscle mass phenotype exhibited a higher point estimate than the combined phenotype. For total fat mass, with Q1 as reference, intermediate quartiles exhibited significantly lower risk (Q2: HR = 0.71, 95% CI: 0.57-0.88; Q3: HR = 0.68, 95% CI: 0.54-0.87), while Q4 showed a similar but non-significant downward trend (HR = 0.64, 95% CI: 0.50-1.03).</p><p><strong>Conclusions: </strong>Among U.S. adults with osteopenia or osteoporosis, low muscle mass was a robust predictor of all-cause mortality. Adiposity defined by body fat percentage was not independently associated with mortality, and fat mass demonstrated a nonlinear pattern with the lowest risk at intermediate levels. These findings support incorporating muscle assessment and refined adiposity measures into risk stratification beyond BMD alone.</p><p><strong>Clinical trial registration: </strong>Not applicable.</p>","PeriodicalId":520640,"journal":{"name":"Hormones (Athens, Greece)","volume":" ","pages":""},"PeriodicalIF":2.5000,"publicationDate":"2026-09-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Hormones (Athens, Greece)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1007/s42000-026-00825-9","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Adults with osteopenia or osteoporosis have increased risks of adverse outcomes; however, mortality risk varies substantially and may be influenced by body composition. Evidence for the joint impact of low muscle mass and percentage-based adiposity in this population remains limited.
Objectives: To examine the independent and combined associations of low muscle mass and obesity with all-cause mortality among U.S. adults with osteopenia or osteoporosis and to characterize the dose-response relationship between total fat mass and mortality.
Methods: We performed a retrospective cohort analysis of NHANES cycles with concurrent whole-body DXA (appendicular lean mass and total fat mass) and site-specific BMD assessments (1999-2006, 2013-2014, and 2017-2018). Eligible participants with osteopenia or osteoporosis and mortality linkage were included (unweighted n = 3,918). Low muscle mass (LMM) was defined by DXA-derived appendicular lean mass index (ALMI; men < 7.0 kg/m², women < 5.5 kg/m²), while obesity was operationally defined by DXA body fat percentage (FM%; men > 30%, women > 42%) instead of body mass index (BMI). Survey-weighted Cox models and restricted cubic splines were utilized.
Results: Over a median follow-up of 14.8 years, 1,095 deaths occurred. In fully adjusted models, low muscle mass was associated with higher mortality (HR = 1.59, 95% CI: 1.30-1.95). Jointly, both low muscle mass alone (HR = 1.70, 95% CI: 1.30-2.23) and low muscle mass with obesity (HR = 1.45, 95% CI: 1.13-1.87) were associated with higher mortality compared with the normal phenotype, whereas obesity alone was not; notably, the isolated low muscle mass phenotype exhibited a higher point estimate than the combined phenotype. For total fat mass, with Q1 as reference, intermediate quartiles exhibited significantly lower risk (Q2: HR = 0.71, 95% CI: 0.57-0.88; Q3: HR = 0.68, 95% CI: 0.54-0.87), while Q4 showed a similar but non-significant downward trend (HR = 0.64, 95% CI: 0.50-1.03).
Conclusions: Among U.S. adults with osteopenia or osteoporosis, low muscle mass was a robust predictor of all-cause mortality. Adiposity defined by body fat percentage was not independently associated with mortality, and fat mass demonstrated a nonlinear pattern with the lowest risk at intermediate levels. These findings support incorporating muscle assessment and refined adiposity measures into risk stratification beyond BMD alone.