Moon Seong-Su
Department of Internal Medicine, Dongguk University College of Medicine, Gyeongju, South Korea.
Endocr J. 2014;61(1):61-70. doi: 10.1507/endocrj.ej13-0244. Epub 2013 Oct 1.
Sarcopenia is an emerging risk factor for metabolic disorders. No study of the association of sarcopenia with insulin resistance, diabetes, and metabolic syndrome (MS) according to age group and obesity status in the general population has been reported. We investigated these associations in the Korean population. Participants included 4558 males and 5874 females, who were ≥20 years of age or older from the fourth and fifth Korea National Health and Nutritional Examination Surveys of the Korean population (2009 and 2010). Age was categorized according to three groups (20-39, 40-59, and ≥ 60 years). Obesity was defined according to body mass index. Sarcopenia was defined as the appendicular skeletal muscle mass (ASM) divided by weight (Wt) (%) of > 2SD below the sex-specific mean for young adults. Homeostasis model assessment of insulin resistance (HOMA-IR) was calculated. After adjustment for confounding variables, sarcopenia showed a significant association with HOMA-IR in the non-obese group (P<0.001). Sarcopenia was found to be a risk factor for diabetes in the non-obese group (OR, 2.140; 95% CI, 1.549-2.956; P<0.001). Sarcopenia also showed an association with MS in the non-obese group (OR, 2.209; 95% CI, 1.679-2.906; P<0.001), but not in the obese-group. However, these results were not relevant to young age group. In conclusion, sarcopenia showed an association with insulin resistance, diabetes, and MS, in the non-obese population. Sarcopenia may be an early predictor for diabetes and MS susceptibility in the non-obese population, particularly in elderly people.
肌肉减少症是代谢紊乱的一个新出现的风险因素。目前尚无关于一般人群中按年龄组和肥胖状况划分的肌肉减少症与胰岛素抵抗、糖尿病和代谢综合征(MS)之间关联的研究报道。我们在韩国人群中调查了这些关联。参与者包括来自韩国第四次和第五次国民健康与营养检查调查(2009年和2010年)的4558名男性和5874名女性,年龄在20岁及以上。年龄分为三组(20 - 39岁、40 - 59岁和≥60岁)。肥胖根据体重指数定义。肌肉减少症定义为四肢骨骼肌质量(ASM)除以体重(Wt)(%),低于年轻成年人特定性别平均值2个标准差以上。计算胰岛素抵抗的稳态模型评估(HOMA - IR)。在对混杂变量进行调整后,肌肉减少症在非肥胖组中与HOMA - IR存在显著关联(P<0.001)。在非肥胖组中发现肌肉减少症是糖尿病的一个风险因素(OR,2.140;95%CI,1.549 - 2.956;P<0.001)。肌肉减少症在非肥胖组中也与MS存在关联(OR,2.209;95%CI,1.679 - 2.906;P<0.001),但在肥胖组中无此关联。然而,这些结果与年轻年龄组无关。总之,在非肥胖人群中,肌肉减少症与胰岛素抵抗、糖尿病和MS存在关联。肌肉减少症可能是非肥胖人群,尤其是老年人中糖尿病和MS易感性的早期预测指标。