Department of Endocrinology and Diabetes, the First Affiliated Hospital of Xiamen University, School of Medicine, Xiamen University, Xiamen, China.
National Institute for Data Science in Health and Medicine, Xiamen University, Xiamen, China.
Int J Obes (Lond). 2024 Jun;48(6):891-899. doi: 10.1038/s41366-024-01493-8. Epub 2024 Feb 21.
This study aims to estimate the prevalence of early-onset sarcopenia and sarcopenic obesity in the United States and its relative risk due to obstructive sleep apnea (OSA).
Data in this cross-sectional study were extracted from the National Health and Nutritional Examination Survey (NHANES) 2015-2018. Weighted multistage stratified probability sampling design was considered to estimate the prevalence of early-onset sarcopenia and sarcopenic obesity. Weighted multivariable logistic regression analyses and weighted multivariable mediation models were performed to evaluate the association between OSA and early-onset sarcopenia.
The prevalence of early-onset sarcopenia and early-onset sarcopenic obesity was estimated to be 5.5% and 4.6%, respectively. A higher prevalence of sarcopenia (12% V.S. 5.5%, P < 0.01) and sarcopenic obesity (10.3% V.S. 4.0%, P < 0.01) was observed among participants with OSA than those without OSA. Multivariable logistic regression models suggested that participants with OSA had higher odds ratios of suffering from early-onset sarcopenia [Odds Ratio (OR): 1.5, 95% confidence interval (CI):1.1-2.7] and early-onset sarcopenic obesity [OR: 1.8, 95% CI: 1.1-3.1] after adjusting for potential confounding variables. Mediation analyses suggested serum chronic reaction protein (CRP) mediated 23.7% (P < 0.01) & 26.2% (P < 0.01), homeostasis model assessment insulin resistance index (HOMA-IR) mediated 24.8% (P < 0.01) & 20.7% (P < 0.05), body mass index (BMI) mediated 46.4% (P < 0.05) & 49.9% (P < 0.01), HEI-2015 mediated 23.3% (P < 0.01) & 25.6% (P < 0.01), and Vitamin D mediated 7.5% (P < 0.01) & 8.5% (P < 0.01) of the potential effects of OSA on early-onset sarcopenia and sarcopenic obesity, respectively.
Early-onset sarcopenia and sarcopenic obesity were prevalent among young adults in the US. OSA is a significant independent risk factor and may induce muscle loss by unhealthy diet habits, higher BMI, chronic inflammation, insulin resistance, and Vitamin D. It was essential for clinicians to arrange appropriate screening and interventions for patients with OSA to prevent muscle loss as early as possible.
本研究旨在估计美国早期发生的肌少症和肌少症性肥胖的流行率及其与阻塞性睡眠呼吸暂停(OSA)的相对风险。
本横断面研究的数据来自 2015-2018 年全国健康和营养检查调查(NHANES)。采用加权多阶段分层概率抽样设计来估计早期发生的肌少症和肌少症性肥胖的流行率。采用加权多变量逻辑回归分析和加权多变量中介模型来评估 OSA 与早期发生的肌少症之间的关系。
估计早期发生的肌少症和早期发生的肌少症性肥胖的流行率分别为 5.5%和 4.6%。与无 OSA 的参与者相比,有 OSA 的参与者的肌少症(12%比 5.5%,P<0.01)和肌少症性肥胖(10.3%比 4.0%,P<0.01)患病率更高。多变量逻辑回归模型表明,在调整了潜在混杂变量后,有 OSA 的参与者发生早期发生的肌少症的比值比(OR)为 1.5(95%置信区间(CI):1.1-2.7)和早期发生的肌少症性肥胖的比值比(OR)为 1.8(95%CI:1.1-3.1)。中介分析表明,血清慢性反应蛋白(CRP)介导了 23.7%(P<0.01)和 26.2%(P<0.01),稳态模型评估胰岛素抵抗指数(HOMA-IR)介导了 24.8%(P<0.01)和 20.7%(P<0.05),身体质量指数(BMI)介导了 46.4%(P<0.05)和 49.9%(P<0.01),HEI-2015 介导了 23.3%(P<0.01)和 25.6%(P<0.01),维生素 D 介导了 OSA 对早期发生的肌少症和肌少症性肥胖的潜在影响的 7.5%(P<0.01)和 8.5%(P<0.01)。
肌少症和肌少症性肥胖在年轻的美国成年人中较为普遍。OSA 是一个显著的独立危险因素,可能通过不健康的饮食习惯、较高的 BMI、慢性炎症、胰岛素抵抗和维生素 D 导致肌肉损失。临床医生有必要为 OSA 患者安排适当的筛查和干预措施,以尽早预防肌肉损失。