Tokyo Metropolitan Institute of Gerontology, Tokyo, Japan.
National Institute for Longevity Sciences, Aichi, Japan.
J Am Med Dir Assoc. 2015 Jan;16(1):85.e1-8. doi: 10.1016/j.jamda.2014.10.006. Epub 2014 Nov 17.
Several studies have explored the prevalence and risk factors of sarcopenia, but they have been based on cross-sectional data. The objective of this study was to determine the incidence and predictors of the onset of sarcopenia over 4 years in community-dwelling elderly women.
Four-year longitudinal follow-up study.
Urban community in Tokyo, Japan.
A total of 538 nonsarcopenic women older than 75 years.
Body composition was determined by bioelectrical impedance analysis. Functional fitness measurements, including grip strength, usual walking speed, timed up and go (TUG), and interview surveys were conducted at baseline and 4-year follow-up. Blood samples were obtained to analyze serum albumin and hemoglobin A1c, and kidney function was analyzed using serum creatinine and cystatin C. Sarcopenia was defined based on the criteria suggested by the European Working Group on Sarcopenia in Older People, and the development of all stages, that is, presarcopenia, sarcopenia, and severe sarcopenia as well as the components of sarcopenia skeletal muscle index (SMI), grip strength, and walking speed, were analyzed.
The incidence of total sarcopenia was 39.6% (presarcopenia 23.8%, sarcopenia 11.2%, severe sarcopenia 4.6%). Older age was significantly predictive of the development of presarcopenia and severe sarcopenia. Body mass index (BMI) lower than 21.0 kg/m(2) was significantly predictive of the development of all stages of sarcopenia, as well as declines in SMI, grip strength, and walking speed. Slow TUG was a predictor of the development of presarcopenia and severe sarcopenia. Increased calf circumference showed protective effects from the development of all stages of sarcopenia. Greater albumin levels also showed lower risk of declines in SMI, walking speed, and development of presarcopenia. Cystatin C was positively associated with the development of severe sarcopenia (odds ratio 1.83, 95% confidence interval 1.08-3.12). Heart disease and hyperlipidemia history were associated with presarcopenia and sarcopenia, respectively.
Age, BMI, calf circumference, and TUG were consistent predictors of the various stages and components of sarcopenia. The data also suggest that cystatin C was associated with higher odds of incident severe sarcopenia, and further study into kidney function and onset of sarcopenia in large populations is needed.
已有多项研究探讨了肌少症的流行率和风险因素,但这些研究都是基于横断面数据。本研究旨在确定社区居住的老年女性在 4 年内发生肌少症的发生率和预测因素。
四年纵向随访研究。
日本东京的城市社区。
共纳入 538 名年龄大于 75 岁且无肌少症的女性。
通过生物电阻抗分析确定身体成分。功能适应性测试,包括握力、常规步行速度、计时起立行走测试(TUG)和访谈调查,在基线和 4 年随访时进行。采集血样以分析血清白蛋白和糖化血红蛋白,使用血清肌酐和胱抑素 C 分析肾功能。肌少症根据欧洲老年人肌少症工作组的标准定义,分析所有阶段(即预肌少症、肌少症和严重肌少症)以及肌少症的组成部分(骨骼肌指数(SMI)、握力和步行速度)的发展情况。
总肌少症的发生率为 39.6%(预肌少症 23.8%,肌少症 11.2%,严重肌少症 4.6%)。年龄较大与预肌少症和严重肌少症的发生显著相关。BMI 低于 21.0kg/m2 与所有阶段肌少症的发生以及 SMI、握力和步行速度的下降显著相关。TUG 较慢是预肌少症和严重肌少症发生的预测因子。增加小腿围度对所有阶段肌少症的发生有保护作用。较高的白蛋白水平也显示出较低的 SMI、步行速度下降和预肌少症发生的风险。胱抑素 C 与严重肌少症的发生呈正相关(比值比 1.83,95%置信区间 1.08-3.12)。心脏病和高脂血症病史分别与预肌少症和肌少症相关。
年龄、BMI、小腿围度和 TUG 是肌少症各阶段和组成部分的一致预测因子。数据还表明,胱抑素 C 与发生严重肌少症的几率较高相关,需要在更大的人群中进一步研究肾功能和肌少症的发病情况。