Han Der-Sheng, Chu-Su Yu, Chiang Chih-Kang, Tseng Fen-Yu, Tseng Ping-Huei, Chen Chi-Ling, Wu Kwan-Dun, Yang Wei-Shiung
Department of Physical Medicine and Rehabilitation, National Taiwan University Hospital BeiHu Branch, Taipei, Taiwan; Department of Physical Medicine and Rehabilitation, National Taiwan University Hospital, Taipei, Taiwan; Graduate Institute of Clinical Medicine, College of Medicine, National Taiwan University, Taipei, Taiwan.
Department of Laboratory Medicine, National Taiwan University Hospital, Taipei, Taiwan; Institute of Biomedical Engineering, National Taiwan University, Taipei, Taiwan.
PLoS One. 2014 Sep 25;9(9):e108230. doi: 10.1371/journal.pone.0108230. eCollection 2014.
Myostatin is a negative regulator of skeletal muscle mass and may also modulate energy metabolism secondarily. We aim to investigate the relationship between serum myostatin and the metabolic variables in diabetic (DM) and non-diabetic subjects.
A cross-sectional study recruiting 246 consecutive DM patients and 82 age- and gender-matched non-diabetic individuals at a medical center was conducted. The variables of anthropometry and blood chemistry were obtained. Serum myostatin level was measured with enzyme immunoassay.
DM group had lower serum myostatin compared with non-diabetics (7.82 versus 9.28 ng/ml, p<0.01). Sixty-two percent of the recruited individuals had metabolic syndrome (MetS). The patients with MetS had significantly lower serum myostatin than those without (7.39 versus 9.49 ng/ml, p<0.001). The serum myostatin level decreased with increasing numbers of the MetS components (p for trend<0.001). The patients with higher body mass index, larger abdominal girth, lower high-density lipoprotein cholesterol (HDL-C), and higher triglycerides had lower serum myostatin than those without. The serum myostatin level was independently negatively related to larger abdominal girth, higher triglycerides, and lower HDL-C after adjustment. The odds ratios for MetS, central obesity, low HDL-C, high triglycerides, and DM were 0.85, 0.88, 0.89, 0.85, and 0.92, respectively, when serum myostatin increased per 1 ng/mL, in the binary logistic regression models.
Lower serum myostatin independently associated with MetS, central obesity, low HDL-C, and high triglycerides after adjustment. Higher serum myostatin is associated with favorable metabolic profiles.
肌肉生长抑制素是骨骼肌质量的负调节因子,也可能继发调节能量代谢。我们旨在研究糖尿病(DM)和非糖尿病受试者血清肌肉生长抑制素与代谢变量之间的关系。
在一家医疗中心进行了一项横断面研究,连续招募了246例DM患者和82例年龄及性别匹配的非糖尿病个体。获取人体测量学和血液化学变量。采用酶免疫测定法测量血清肌肉生长抑制素水平。
DM组血清肌肉生长抑制素水平低于非糖尿病组(7.82对9.28 ng/ml,p<0.01)。62%的招募个体患有代谢综合征(MetS)。患有MetS的患者血清肌肉生长抑制素水平显著低于未患MetS的患者(7.39对9.49 ng/ml,p<0.001)。血清肌肉生长抑制素水平随MetS组分数量增加而降低(趋势p<0.001)。体重指数较高、腹围较大、高密度脂蛋白胆固醇(HDL-C)较低和甘油三酯较高的患者血清肌肉生长抑制素水平低于无这些情况的患者。调整后,血清肌肉生长抑制素水平与较大腹围、较高甘油三酯和较低HDL-C独立呈负相关。在二元逻辑回归模型中,当血清肌肉生长抑制素每增加1 ng/mL时,MetS、中心性肥胖、低HDL-C、高甘油三酯和DM的比值比分别为0.85、0.88、0.89、0.85和0.92。
调整后,较低的血清肌肉生长抑制素与MetS、中心性肥胖、低HDL-C和高甘油三酯独立相关。较高的血清肌肉生长抑制素与良好的代谢特征相关。