Liu Jia, Zhang Fuchun
Department of Geriatrics, Peking University Third Hospital, Beijing, China.
Front Med (Lausanne). 2025 Jul 10;12:1515839. doi: 10.3389/fmed.2025.1515839. eCollection 2025.
Sarcopenia is linked to increased mortality, but the specific role of inflammation in sarcopenia-related mortality remains poorly understood. This study aims to integrate various inflammatory biomarkers to develop an inflammation prognostic score (IPS) within the large, representative NHANES cohort. It also explores the association between sarcopenia, inflammatory markers, and mortality, and investigates whether inflammation mediates this relationship.
This study analyzed data from NHANES (1999-2006) on 3,544 participants aged 65 and older, with mortality follow-up through December 31, 2019, using death records from the National Death Index (NDI). Statistical analyses accounted for complex survey design and multiple imputation for missing data. Sarcopenia was defined using appendicular skeletal mass (ASM) adjusted for body mass index (BMI). Cox regression assessed the association between sarcopenia, inflammatory markers, and all-cause mortality. The IPS was developed using LASSO regression, and mediation analysis was conducted to assess whether inflammatory markers mediate the relationship between sarcopenia and mortality.
Among 3,544 elderly participants, sarcopenia was present in 25.4%, with a 66.6% overall mortality rate during the follow-up period. Multivariate Cox regression confirmed that sarcopenia is an independent risk factor for mortality [Hazard ratio (HR) = 1.235-1.281, < 0.001]. Inflammatory markers were significantly associated with all-cause mortality. The IPS showed a clear trend of increasing mortality risk across quartiles, with HR reaching 2.044 in Q4 ( < 0.001). Mediation analysis showed that IPS mediated 20.8% of the relationship between sarcopenia and mortality, with the mediating effect remaining significant after adjusting for confounders.
This study confirms the association between sarcopenia and increased mortality risk, with inflammation as a key mediating factor, highlighting its role in sarcopenia-related mortality.
肌肉减少症与死亡率增加相关,但炎症在肌肉减少症相关死亡率中的具体作用仍知之甚少。本研究旨在整合各种炎症生物标志物,在具有代表性的大型美国国家健康与营养检查调查(NHANES)队列中开发一种炎症预后评分(IPS)。本研究还探讨了肌肉减少症、炎症标志物与死亡率之间的关联,并研究炎症是否介导了这种关系。
本研究分析了NHANES(1999 - 2006年)中3544名65岁及以上参与者的数据,并通过国家死亡指数(NDI)的死亡记录对其进行了至2019年12月31日的死亡率随访。统计分析考虑了复杂的调查设计和对缺失数据的多重填补。肌肉减少症采用根据体重指数(BMI)调整后的四肢骨骼肌质量(ASM)来定义。Cox回归评估了肌肉减少症、炎症标志物与全因死亡率之间的关联。使用LASSO回归开发IPS,并进行中介分析以评估炎症标志物是否介导了肌肉减少症与死亡率之间的关系。
在3544名老年参与者中,25.4%存在肌肉减少症,随访期间总死亡率为66.6%。多变量Cox回归证实,肌肉减少症是死亡率的独立危险因素[风险比(HR) = 1.235 - 1.281,< 0.001]。炎症标志物与全因死亡率显著相关。IPS显示出死亡率风险在四分位数间呈明显上升趋势,在第四四分位数中HR达到2.044(< 0.001)。中介分析表明,IPS介导了肌肉减少症与死亡率之间20.8%的关系,在调整混杂因素后中介效应仍然显著。
本研究证实了肌肉减少症与死亡率增加风险之间的关联,炎症是关键的中介因素,突出了其在肌肉减少症相关死亡率中的作用。