Álvarez-Bustos Alejandro, Carnicero Jose A, Sepúlveda-Loyola Walter, Molina-Baena Begoña, Garcia-Garcia Francisco J, Rodríguez-Mañas Leocadio
Centro de Investigación Biomédica en Red sobre Fragilidad y Envejecimiento Saludable (CIBERFES), Instituto de Salud Carlos III, Madrid, Spain.
Instituto de Investigación IdiPaz, Madrid, Spain.
Innov Aging. 2025 Mar 28;9(5):igaf021. doi: 10.1093/geroni/igaf021. eCollection 2025.
Sarcopenic obesity (SO), obesity, and sarcopenia have been related to adverse events in older adults, raising the question about the role of each component in the risk associated with SO. The objective of this manuscript is to evaluate the role of sarcopenia, obesity, and its interaction in the risks (frailty, disability, mortality) associated with sarcopenic obesity.
Data from the Toledo Study of Healthy Aging (TSHA) were used. This is a cohort-based study composed of community-dwelling adults ≥65 years. Obesity (Body Mass Index-BMI ≥30) and sarcopenia (the Foundation for the National Institutes of Health-FNIH criteria, standardized to our population) were assessed at baseline. Frailty, through the Frailty Phenotype (FP) and the Frailty Trait scale-5 (FTS5), and disability (Katz Index) were evaluated at baseline. Mortality, frailty, and disability were assessed at follow-up. Logistic (odds ratio, OR) and Cox (hazard ratio, HR) regression models were computed to assess the associations.
A total of 1 538 (74.73 years, 45.51% men) individuals were included. Cross-sectionally, SO, sarcopenia, and obesity were significantly associated with the risk of frailty and disability. Longitudinally, Sarcopenia was associated with all the adverse events (ORs/HRs ranged from 1.41 to 4.14, -value < .05); whereas SO [FP, OR (95% confidence interval-CI): 4.27 (2.05, 8.93); FTS5, OR (95% CI): 6.14 (3.58, 10.51), -value < .001] and obesity [FP, OR (95% CI): 3.10 (1.95, 4.94), -value < 0.001; FTS5, OR (95% CI): 2.26 (1.17, 4.35), -value 0.015] was only associated with incident frailty. Sarcopenia added risk to obesity for frailty (FP and FTS5) whereas obesity only did for frailty (FTS5) in sarcopenic individuals. The interaction between sarcopenia and obesity was not associated with any outcome.
Sarcopenia and obesity provide each other an additive risk for frailty, but not a multiplicative (ie, interaction) one, in sarcopenic obesity. Sarcopenia is the mean factor accounting for the associated risk.
肌少症性肥胖(SO)、肥胖症和肌少症与老年人的不良事件相关,这引发了关于每个组成部分在与SO相关风险中所起作用的疑问。本论文的目的是评估肌少症、肥胖症及其相互作用在与肌少症性肥胖相关的风险(衰弱、残疾、死亡率)中的作用。
使用了来自托莱多健康老龄化研究(TSHA)的数据。这是一项基于队列的研究,由年龄≥65岁的社区居住成年人组成。在基线时评估肥胖症(体重指数 - BMI≥30)和肌少症(美国国立卫生研究院基金会 - FNIH标准,根据我们的人群进行标准化)。在基线时通过衰弱表型(FP)和衰弱特质量表 - 5(FTS5)评估衰弱情况,并通过Katz指数评估残疾情况。在随访时评估死亡率、衰弱情况和残疾情况。计算逻辑(优势比,OR)和Cox(风险比,HR)回归模型以评估关联。
共纳入1538名个体(74.73岁,45.51%为男性)。横断面分析显示,SO、肌少症和肥胖症与衰弱和残疾风险显著相关。纵向分析表明,肌少症与所有不良事件相关(ORs/HRs范围为1.41至4.14,P值<0.05);而SO [FP,OR(95%置信区间 - CI):4.27(2.05,8.93);FTS5,OR(95%CI):6.14(3.58,10.51),P值<0.001]和肥胖症[FP,OR(95%CI):3.10(1.95,4.94),P值<0.001;FTS5,OR(95%CI):2.26(1.17,4.35),P值0.015]仅与新发衰弱相关。在肌少症个体中,肌少症增加了肥胖症导致衰弱的风险(FP和FTS5),而肥胖症仅在肌少症个体中增加了导致衰弱(FTS5)的风险。肌少症和肥胖症之间的相互作用与任何结局均无关联。
在肌少症性肥胖中,肌少症和肥胖症相互增加了衰弱的风险,但不是相乘(即相互作用)的风险。肌少症是导致相关风险的主要因素。