Wu Tianxing, Wang Xiaoshuai, Cai Zhuojian, Cao Peihua, Dang Qin, Zhou Weijie, Xie Jiawei, Chen Jie, Wang Taiwei, Tao Gaochenzi, Han Weiyu, Zhu Zhaohua, Wang Jian, Hunter David J, Barazzoni Rocco, Ding Changhai, Li Jia
Division of Orthopaedic Surgery, Department of Orthopedics, Nanfang Hospital, Southern Medical University and Clinical Research Centre and The Second School of Clinical Medicine, Zhujiang Hospital, Southern Medical University, Guangzhou, China.
Clinical Research Centre, Zhujiang Hospital, Southern Medical University, Guangzhou, China.
Arthritis Rheumatol. 2025 Oct;77(10):1362-1372. doi: 10.1002/art.43213. Epub 2025 Jun 19.
Sarcopenia and knee osteoarthritis (KOA) are common conditions in older adults, but their relationship is controversial. We aimed to examine the potential role of sarcopenia in KOA progression and subsequent knee replacement (KR).
Using data from the Osteoarthritis Initiative, baseline sarcopenia was first screened according to the EWGSOP2 algorithm using the SARC-F (Strength, Assistance with walking, Rise from a chair, Climb stairs, and Falls) questionnaire (screened sarcopenia [Scre-S]), then further assessed combined with the five times chair-stand-test (probable sarcopenia [Prob-S]). Radiographic KOA progression was evaluated by changes in Kellgren-Lawrence Grade and Osteoarthritis Research Society International atlas scores from baseline to the 24- and 48-month follow-ups. Symptomatic progression was evaluated similarly using the Western Ontario McMaster Osteoarthritis Index. The associations of sarcopenia with radiographic or symptomatic progression and subsequent KR were analyzed before and after adjusting for potential confounders and propensity score (PS) matching.
A total of 4,316 participants were included; 27.2% were Scre-S and 16.8% were Prob-S. Baseline Scre-S and Prob-S were positively associated with both radiographic and symptomatic progression in KOA over 24 and 48 months. Both Scre-S and Prob-S were associated with a higher risk of subsequent KR (Scre-S: hazard ratio [HR] 3.84, 95% confidence interval [CI] 3.18 to 4.62; Prob-S: HR 2.29, 95% CI 1.87 to 2.81). These results remained significant in the PS-matched cohort.
Scre-S and Prob-S were significantly and longitudinally associated with both radiographic and symptomatic progression in KOA and subsequent KR. Our findings indicated a potential causal role of sarcopenia in KOA progression and highlighted its potentially therapeutic effect in KOA management.
肌肉减少症和膝关节骨关节炎(KOA)是老年人的常见病症,但它们之间的关系存在争议。我们旨在研究肌肉减少症在KOA进展及随后膝关节置换(KR)中的潜在作用。
利用骨关节炎倡议组织的数据,首先根据EWGSOP2算法,使用SARC-F(力量、行走辅助、从椅子上起身、爬楼梯和跌倒)问卷筛查基线肌肉减少症(筛查出的肌肉减少症[Scre-S]),然后结合五次椅子站立测试进行进一步评估(可能的肌肉减少症[Prob-S])。通过从基线到24个月和48个月随访时Kellgren-Lawrence分级和国际骨关节炎研究学会图谱评分的变化来评估影像学KOA进展。使用西安大略和麦克马斯特大学骨关节炎指数以类似方式评估症状进展。在调整潜在混杂因素和倾向评分(PS)匹配前后,分析肌肉减少症与影像学或症状进展以及随后KR之间的关联。
共纳入4316名参与者;27.2%为Scre-S,16.8%为Prob-S。基线Scre-S和Prob-S与24个月和48个月期间KOA的影像学和症状进展均呈正相关。Scre-S和Prob-S均与随后KR的较高风险相关(Scre-S:风险比[HR] 3.84,95%置信区间[CI] 3.18至4.62;Prob-S:HR 2.29,95% CI 1.87至2.81)。这些结果在PS匹配队列中仍然显著。
Scre-S和Prob-S与KOA的影像学和症状进展以及随后的KR均存在显著的纵向关联。我们的研究结果表明肌肉减少症在KOA进展中具有潜在因果作用,并突出了其在KOA管理中的潜在治疗效果。