Department of Pediatrics, University of Virginia School of Medicine, Charlottesville, Virginia, USA.
Metab Syndr Relat Disord. 2010 Aug;8(4):343-53. doi: 10.1089/met.2010.0008.
The aim of this study was to compare currently proposed sets of pediatric metabolic syndrome criteria for the ability to predict elevations in "surrogate" factors that are associated with metabolic syndrome and with future cardiovascular disease and type 2 diabetes mellitus. These surrogate factors were fasting insulin, hemoglobin A1c (HbA1c), high-sensitivity C-reactive protein (hsCRP), and uric acid.
Waist circumference (WC), blood pressure, triglycerides, high-density lipoprotein cholesterol (HDL-C), fasting glucose, fasting insulin, HbA1c, hsCRP, and uric acid measurements were obtained from 2,624 adolescent (12-18 years old) participants of the 1999-2006 National Health and Nutrition Examination Surveys. We identified children with metabolic syndrome as defined by six commonly used sets of pediatric metabolic syndrome criteria. We then defined elevations in the surrogate factors as values in the top 5% for the cohort and calculated sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) for each set of metabolic syndrome criteria and for each surrogate factor.
Current pediatric metabolic syndrome criteria exhibited variable sensitivity and specificity for surrogate predictions. Metabolic syndrome criteria had the highest sensitivity for predicting fasting insulin (40-70%), followed by uric acid (31-54%), hsCRP (13-31%), and HbA1c (7-21%). The criteria of de Ferranti (which includes children with WC >75(th) percentile, compared to all other sets including children with WC >90(th) percentile) exhibited the highest sensitivity for predicting each of the surrogates, with only modest decrease in specificity compared to the other sets of criteria. However, the de Ferranti criteria also exhibited the lowest PPV values. Conversely, the pediatric International Diabetes Federation criteria exhibited the lowest sensitivity and the highest specificity.
Pediatric metabolic syndrome criteria exhibit moderate sensitivity for detecting elevations in surrogate factors associated with metabolic syndrome and with risk for future disease. Inclusion of children with more modestly elevated WC improved sensitivity.
本研究旨在比较目前提出的几套儿科代谢综合征标准,以评估其预测与代谢综合征及未来心血管疾病和 2 型糖尿病相关的“替代”因素升高的能力。这些替代因素包括空腹胰岛素、糖化血红蛋白(HbA1c)、高敏 C 反应蛋白(hsCRP)和尿酸。
从 1999-2006 年全国健康和营养调查中 2624 名青少年(12-18 岁)参与者中获取腰围(WC)、血压、甘油三酯、高密度脂蛋白胆固醇(HDL-C)、空腹血糖、空腹胰岛素、HbA1c、hsCRP 和尿酸测量值。我们将符合六种常用儿科代谢综合征标准之一的儿童定义为代谢综合征患者。然后,我们将替代因素的升高定义为队列中前 5%的值,并计算每套代谢综合征标准和每个替代因素的敏感性、特异性、阳性预测值(PPV)和阴性预测值(NPV)。
目前的儿科代谢综合征标准在替代预测方面表现出不同的敏感性和特异性。代谢综合征标准对空腹胰岛素的预测敏感性最高(40-70%),其次是尿酸(31-54%)、hsCRP(13-31%)和 HbA1c(7-21%)。与其他包括 WC>90 百分位的儿童的所有标准相比,包含 WC>75 百分位的儿童的 de Ferranti 标准对每个替代因素的预测敏感性最高,特异性仅略有下降。然而,de Ferranti 标准的 PPV 值也最低。相反,儿科国际糖尿病联盟标准的敏感性最低,特异性最高。
儿科代谢综合征标准对检测与代谢综合征及未来疾病风险相关的替代因素升高具有中等敏感性。纳入 WC 略有升高的儿童可提高敏感性。