Wu Chung-Ze, Lin Jiunn-Diann, Li Jer-Chuan, Hsiao Fone-Ching, Hsieh Chang-Hsun, Kuo Shi-Wen, Hung Yi-Jen, Lu Chieh-Hua, He Chih-Tsueng, Pei Dee
Department of Internal Medicine, Buddhist Tzu Chi General Hospital, Taipei Brach, Taiwan, ROC.
Indian J Med Res. 2008 Apr;127(4):336-43.
BACKGROUND & OBJECTIVE: With the increasing prevalence of type 2 diabetes and cardiovascular disease in Taiwan, the understanding of metabolic syndrome (MetS) becomes more important. The purpose of this study was to investigate the clustering patterns of the risk variables of the MetS with factor analysis (FacAn).
A total of 564 Chinese individuals with normal glucose tolerance (N, n=345), impaired glucose tolerance (IGT, n=164) or diabetes mellitus (DM, n=55) were enrolled. Insulin resistance was measured by insulin suppression test (IST). The components of MetS such as waist hip ratio (WHR), fasting plasma glucose (FPG), systolic blood pressure (SBP), diastolic blood pressure (DBP), triglyceride (TG), high density lipoprotein cholesterol (HDLC) and steady state plasma glucose (SSPG) from IST were put into the model of exploratory FacAn.
In spite of the minor different loading patterns, three dimensions were identified in the three subgroups; a "blood pressure" dimension, loading with mainly SBP and DBP, an "insulin resistance" dimension, loading mainly with SSPG, and an "adiposity/glucose" dimension loading with TG, WHR or FPG.
INTERPRETATION & CONCLUSION: Our results were consistent with different ethnic groups in earlier reports that more than two dimensions were identified and that the MetS is not unified by a single underlying aetiology, i.e., insulin resistance. Longitudinal analysis in this and other populations will be required to validate our findings and to test their generalisability.
随着台湾地区2型糖尿病和心血管疾病患病率的不断上升,对代谢综合征(MetS)的认识变得更加重要。本研究的目的是通过因子分析(FacAn)探讨MetS风险变量的聚类模式。
共纳入564名糖耐量正常(N,n = 345)、糖耐量受损(IGT,n = 164)或糖尿病(DM,n = 55)的中国个体。通过胰岛素抑制试验(IST)测量胰岛素抵抗。将MetS的组成成分,如腰臀比(WHR)、空腹血糖(FPG)、收缩压(SBP)、舒张压(DBP)、甘油三酯(TG)、高密度脂蛋白胆固醇(HDLC)和来自IST的稳态血糖(SSPG)纳入探索性FacAn模型。
尽管各亚组的负荷模式略有不同,但在三个亚组中均识别出三个维度;一个“血压”维度,主要由SBP和DBP负荷,一个“胰岛素抵抗”维度,主要由SSPG负荷,一个“肥胖/血糖”维度由TG、WHR或FPG负荷。
我们的结果与早期报告中不同种族群体的结果一致,即识别出了两个以上的维度,且MetS并非由单一潜在病因(即胰岛素抵抗)统一。需要对本研究人群及其他人群进行纵向分析,以验证我们的发现并检验其普遍性。