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青少年代谢综合征的验证性因子分析:性别和种族/民族差异的检验。

A confirmatory factor analysis of the metabolic syndrome in adolescents: an examination of sex and racial/ethnic differences.

机构信息

Department of Biostatistics, School of Public Health, West Virginia University, Morgantown, West Virginia, USA.

出版信息

Cardiovasc Diabetol. 2012 Oct 13;11:128. doi: 10.1186/1475-2840-11-128.

Abstract

OBJECTIVE

The metabolic syndrome (MetS) is a cluster of clinical indices that signals increased risk for cardiovascular disease and Type 2 diabetes. The diagnosis of MetS is typically based on cut-off points for various components, e.g. waist circumference and blood pressure. Because current MetS criteria result in racial/ethnic discrepancies, our goal was to use confirmatory factor analysis to delineate differential contributions to MetS by sub-group.

RESEARCH DESIGN AND METHODS

Using 1999-2010 data from the National Health and Nutrition Examination Survey (NHANES), we performed a confirmatory factor analysis of a single MetS factor that allowed differential loadings across sex and race/ethnicity, resulting in a continuous MetS risk score that is sex and race/ethnicity-specific.

RESULTS

Loadings to the MetS score differed by racial/ethnic and gender subgroup with respect to triglycerides and HDL-cholesterol. ROC-curve analysis revealed high area-under-the-curve concordance with MetS by traditional criteria (0.96), and with elevations in MetS-associated risk markers, including high-sensitivity C-reactive protein (0.71), uric acid (0.75) and fasting insulin (0.82). Using a cut off for this score derived from ROC-curve analysis, the MetS risk score exhibited increased sensitivity for predicting elevations in ≥2 of these risk markers as compared with traditional pediatric MetS criteria.

CONCLUSIONS

The equations from this sex- and race/ethnicity-specific analysis provide a clinically-accessible and interpretable continuous measure of MetS that can be used to identify children at higher risk for developing adult diseases related to MetS, who could then be targeted for intervention. These equations also provide a powerful new outcome for use in childhood obesity and MetS research.

摘要

目的

代谢综合征(MetS)是一组临床指标,表明心血管疾病和 2 型糖尿病的风险增加。MetS 的诊断通常基于各种成分的截止点,例如腰围和血压。由于目前的 MetS 标准导致了种族/民族差异,我们的目标是使用验证性因子分析来描绘亚组对 MetS 的不同贡献。

研究设计和方法

使用 1999-2010 年国家健康和营养检查调查(NHANES)的数据,我们对单个 MetS 因子进行了验证性因子分析,允许性别和种族/民族之间的差异加载,从而产生了性别和种族/民族特异性的连续 MetS 风险评分。

结果

MetS 评分的加载值因种族/民族和性别亚组而异,与甘油三酯和高密度脂蛋白胆固醇有关。ROC 曲线分析显示,与传统标准(0.96)相比,与 MetS 相关的风险标志物升高的一致性较高,包括高敏 C 反应蛋白(0.71)、尿酸(0.75)和空腹胰岛素(0.82)。使用 ROC 曲线分析得出的该评分的截止值,MetS 风险评分在预测这些风险标志物中的≥2 个标志物升高方面具有更高的敏感性,而不是传统的儿科 MetS 标准。

结论

这些来自性别和种族/民族特异性分析的方程提供了一种临床可及和可解释的 MetS 连续测量方法,可用于识别患有与 MetS 相关的成人疾病风险较高的儿童,然后可以针对这些儿童进行干预。这些方程还为儿童肥胖和 MetS 研究提供了一种强大的新结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbe6/3489601/057beaaaa5a1/1475-2840-11-128-1.jpg

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