Yarnell J W, Patterson C C, Bainton D, Sweetnam P M
Queen's University, Belfast, UK.
Heart. 1998 Mar;79(3):248-52. doi: 10.1136/hrt.79.3.248.
To examine the clinical and epidemiological utility of the concepts of metabolic syndrome and insulin resistance syndrome in two prospective cohort studies of white men.
Men aged 45-63 years were screened for evidence of ischaemic heart disease (IHD) between 1979 and 1982 and followed up at regular intervals thereafter. Non-fatal coronary events were validated from hospital records and fatal coronary events from death certificates.
Analysis of serum insulin concentrations in non-diabetic individuals measured at entry to the study showed no independent contribution to the prediction of subsequent IHD at 10 year follow up. Blood glucose concentrations, however, showed a small independent contribution in the combined cohort in the upper fifth of the distribution. Three different models of metabolic syndrome among non-diabetic individuals were defined based on tertiles, medians, and clusters. The predictive value of each model was assessed using logistic regression before and after adjustment for conventional and metabolic risk factors. After adjustment the odds were non-significant and close to unity.
This study did not detect any complex relation among the five variables defining metabolic syndrome; the excess risk seems to be no greater than can be explained by individual effects of the defining variables in a multiple logistic model.
在两项针对白人男性的前瞻性队列研究中,检验代谢综合征和胰岛素抵抗综合征概念的临床及流行病学效用。
1979年至1982年间,对年龄在45至63岁的男性进行缺血性心脏病(IHD)证据筛查,此后定期随访。非致命性冠状动脉事件通过医院记录核实,致命性冠状动脉事件通过死亡证明核实。
对研究入组时测量的非糖尿病个体血清胰岛素浓度分析显示,在10年随访中,其对后续IHD预测无独立贡献。然而,血糖浓度在分布最高的五分之一联合队列中显示出较小的独立贡献。基于三分位数、中位数和聚类定义了非糖尿病个体中三种不同的代谢综合征模型。在对传统和代谢危险因素进行调整前后,使用逻辑回归评估每个模型的预测价值。调整后,比值无统计学意义且接近1。
本研究未发现定义代谢综合征的五个变量之间存在任何复杂关系;额外风险似乎不超过多变量逻辑模型中定义变量的个体效应所能解释的范围。