Eddy D M, Schlessinger L, Heikes K
Archimedes Inc., San Francisco, CA, USA.
Int J Obes (Lond). 2008 May;32 Suppl 2:S5-10. doi: 10.1038/ijo.2008.28.
The clinical importance of the metabolic syndrome (MeS) is confused by the existence of at least three different definitions proposed by prominent organizations, and by a lack of information about the prognostic value of diagnosing a person as having the syndrome by any of the definitions.
We used the US National Health and Nutrition Evaluation Survey (NHANES) to determine the prevalence in the United States of the variables used to define the MeS and cardiovascular disease (CVD), and to create a simulated population that matched the US population with respect to all the important characteristics, risk factors and treatments for CVD. We then used the Archimedes model to calculate the long-term CVD outcomes for each person in the simulated population.
The definitions implied an increased risk of CVD of 1.5-1.6. The definitions varied considerably in their ability to identify people at risk of myocardial infarctions (MIs); the proportion of people destined to have a future MI captured by the different definitions varied from 57 to 77%. The definitions also varied widely in how well they ruled out future MIs; failure to have MeS by a definition still left a chance of a future MI ranging from 23 to 42%. The definitions differed importantly in which people they identified as having MeS; 34% of those who met the ATP definition did not meet the WHO definition, 30% of those who met the WHO definition did not meet the ATP definition and 28% of those who met the IDF definition did not meet the ATP definition. Of the components of the definitions, the most important single factor for identifying a person at risk of future CVD was high glucose, with hypertension, obesity, high triglycerides and low HDL following in that order. High glucose, by itself, was as good as any definition of the MeS in predicting risk of future MI. Whichever definition was used, individuals who met the definition varied widely in their risk of CVD.
For assessing a particular person's risk of future CVD and for making treatment decisions a diagnosis of MeS by any of the definitions added little if anything to assessing each person's risk factors.
代谢综合征(MeS)的临床重要性因至少三个知名组织提出的不同定义的存在,以及缺乏关于采用任何一种定义诊断一个人患有该综合征的预后价值的信息而变得模糊不清。
我们利用美国国家健康与营养检查调查(NHANES)来确定用于定义MeS和心血管疾病(CVD)的变量在美国的患病率,并创建一个在所有重要特征、风险因素和CVD治疗方面与美国人群相匹配的模拟人群。然后我们使用阿基米德模型来计算模拟人群中每个人的长期CVD结局。
这些定义意味着CVD风险增加1.5 - 1.6倍。这些定义在识别有心肌梗死(MI)风险人群的能力上有很大差异;不同定义所捕捉到的未来会发生MI的人群比例从57%到77%不等。这些定义在排除未来MI的能力方面也有很大差异;根据一种定义未患MeS的人未来发生MI的可能性仍在23%到42%之间。这些定义在确定哪些人患有MeS方面有很大不同;符合ATP定义的人中有34%不符合WHO定义,符合WHO定义的人中有30%不符合ATP定义,符合IDF定义的人中有28%不符合ATP定义。在这些定义的组成部分中,识别未来有CVD风险人群的最重要单一因素是高血糖,其次是高血压、肥胖、高甘油三酯和低高密度脂蛋白。仅高血糖本身在预测未来MI风险方面与MeS的任何定义一样有效。无论使用哪种定义,符合该定义的个体在CVD风险方面差异很大。
对于评估特定个体未来患CVD的风险以及做出治疗决策而言,采用任何一种定义诊断MeS对评估每个人的风险因素几乎没有增加任何价值。