Huang Shih-Tsung, Otsuka Rei, Nishita Yukiko, Meng Lin-Chieh, Hsiao Fei-Yuan, Shimokata Hiroshi, Chen Liang-Kung, Arai Hidenori
Department of Pharmacy, National Yang Ming Chiao Tung University, Taipei, Taiwan.
Center for Healthy Longevity and Aging Sciences, National Yang Ming University, Taipei, Taiwan.
J Cachexia Sarcopenia Muscle. 2025 Feb;16(1):e13660. doi: 10.1002/jcsm.13660. Epub 2024 Dec 16.
Inconsistent results have been reported concerning the association between statin administration and muscle health, specifically its potential to increase the risk of sarcopenia. Given the widespread long-term use of statins among the elderly population, the exploration of this association remains a crucial yet insufficiently examined matter. This study aimed to assess the association between the prolonged administration of statins and the risk of sarcopenia, diminished muscle strength, reduced skeletal muscle mass and impaired physical performance.
This population-based cohort study was conducted in Japan utilizing data derived from the National Institute for Longevity Sciences-Longitudinal Study of Aging (NILS-LSA). The study participants, enlisted from the 2nd to the 6th waves (spanning from April 2000 to July 2010) of NILS-LSA, were those who aged 40 years or older and had initiated statin therapy (n = 348, age: 64.1 years, female: 63.5%). Individuals who were not administered statins (n = 2559, age: 55.5 years, female: 48.4%) were arbitrarily chosen using a combined approach of propensity score (PS) matching and risk set sampling to form the control group (with a 1:4 matching ratio). The primary outcome of this study was the occurrence of sarcopenia, as defined by the 2019 consensus of the Asian Working Group for Sarcopenia (AWGS). The secondary outcomes included low muscle mass (< 7.0 kg/m for men and below 5.4 kg/m for women by DXA), reduced skeletal muscle strength (handgrip strength < 28 kg in men and < 18 kg in women) and subpar physical performance (6-min walking speed < 1.0 m/s). The relationship between the use of statins and the outcomes was estimated using a Cox proportional hazard model with time-varying covariates, which included the status of statin use and other variables (two-tailed p < 0.05 was considered statistically significant). Stratification based on age and sex, along with five sensitivity analyses-including propensity score overlap weighting and a negative control-was conducted.
After applying PS matching, we identified 342 statin initiators and 1294 non-statin users, with well-balanced baseline characteristics between the groups. The use of statins was not associated with an increased risk of incident sarcopenia (adjusted hazard ratio [aHR], 1.43 [95% CI, 0.86, 2.36]), diminished muscle strength (aHR, 1.11 [95% CI, 0.80, 1.54]), reduced muscle mass (aHR, 1.09 [95% CI, 0.66, 1.82]) or impaired physical performance (aHR, 0.73 [95% CI, 0.46, 1.17]). These findings were consistent across age and sex stratifications, as well as all sensitivity analyses.
Statin use was not associated with an elevated risk of sarcopenia or impaired muscle health among community-dwelling middle-aged and older adults in Japan.
关于他汀类药物使用与肌肉健康之间的关联,尤其是其增加肌少症风险的可能性,已有不一致的研究结果报道。鉴于他汀类药物在老年人群中广泛长期使用,对这种关联的探索仍然是一个关键但尚未得到充分研究的问题。本研究旨在评估长期使用他汀类药物与肌少症风险、肌肉力量减弱、骨骼肌质量减少和身体机能受损之间的关联。
本基于人群的队列研究在日本进行,利用了国立长寿医疗研究中心老龄化纵向研究(NILS-LSA)的数据。研究参与者来自NILS-LSA的第2至第6波(从2000年4月至2010年7月),年龄在40岁及以上且已开始他汀类药物治疗(n = 348,年龄:64.1岁,女性:63.5%)。未使用他汀类药物的个体(n = 2559,年龄:55.5岁,女性:48.4%)采用倾向评分(PS)匹配和风险集抽样相结合的方法随机选取,以形成对照组(匹配比例为1:4)。本研究的主要结局是根据亚洲肌少症工作组(AWGS)2019年共识定义的肌少症的发生情况。次要结局包括低肌肉量(男性双能X线吸收法测定< 7.0 kg/m,女性< 5.4 kg/m)、骨骼肌力量减弱(男性握力< 28 kg,女性< 18 kg)和身体机能不佳(6分钟步行速度< 1.0 m/s)。使用Cox比例风险模型对他汀类药物使用与结局之间的关系进行估计,该模型包含随时间变化的协变量,包括他汀类药物使用状态和其他变量(双侧p < 0.05被认为具有统计学意义)。进行了基于年龄和性别的分层,以及五项敏感性分析,包括倾向评分重叠加权和阴性对照。
应用PS匹配后,我们确定了342名开始使用他汀类药物者和1294名未使用他汀类药物者,两组之间的基线特征均衡。使用他汀类药物与新发肌少症风险增加(调整后风险比[aHR],1.43 [95%置信区间,0.86, 2.36])、肌肉力量减弱(aHR,1.11 [95%置信区间,0.80, 1.54])、肌肉量减少(aHR,1.09 [95%置信区间,0.66, 1.82])或身体机能受损(aHR,0.73 [95%置信区间,0.46, 1.17])均无关联。这些发现无论在年龄和性别分层中,还是在所有敏感性分析中均一致。
在日本社区居住的中老年成年人中,使用他汀类药物与肌少症风险升高或肌肉健康受损无关。