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

<p>Abstract</p> <p>Objective</p> <p>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 c...

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Main Authors: Gurka Matthew J, Ice Christa L, Sun Shumei S, DeBoer Mark D
Format: Article
Language:English
Published: BMC 2012-10-01
Series:Cardiovascular Diabetology
Subjects:
Online Access:http://www.cardiab.com/content/11/1/128
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spelling doaj-df0afeee472149458a714931c7de95522020-11-24T21:33:41ZengBMCCardiovascular Diabetology1475-28402012-10-0111112810.1186/1475-2840-11-128A confirmatory factor analysis of the metabolic syndrome in adolescents: an examination of sex and racial/ethnic differencesGurka Matthew JIce Christa LSun Shumei SDeBoer Mark D<p>Abstract</p> <p>Objective</p> <p>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.</p> <p>Research Design and Methods</p> <p>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.</p> <p>Results</p> <p>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.</p> <p>Conclusions</p> <p>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.</p> http://www.cardiab.com/content/11/1/128Metabolic syndromeFactor analysis, StatisticalInsulin resistancePediatricsAdolescentsEpidemiologyClinical studiesObesityRisk factors
collection DOAJ
language English
format Article
sources DOAJ
author Gurka Matthew J
Ice Christa L
Sun Shumei S
DeBoer Mark D
spellingShingle Gurka Matthew J
Ice Christa L
Sun Shumei S
DeBoer Mark D
A confirmatory factor analysis of the metabolic syndrome in adolescents: an examination of sex and racial/ethnic differences
Cardiovascular Diabetology
Metabolic syndrome
Factor analysis, Statistical
Insulin resistance
Pediatrics
Adolescents
Epidemiology
Clinical studies
Obesity
Risk factors
author_facet Gurka Matthew J
Ice Christa L
Sun Shumei S
DeBoer Mark D
author_sort Gurka Matthew J
title A confirmatory factor analysis of the metabolic syndrome in adolescents: an examination of sex and racial/ethnic differences
title_short A confirmatory factor analysis of the metabolic syndrome in adolescents: an examination of sex and racial/ethnic differences
title_full A confirmatory factor analysis of the metabolic syndrome in adolescents: an examination of sex and racial/ethnic differences
title_fullStr A confirmatory factor analysis of the metabolic syndrome in adolescents: an examination of sex and racial/ethnic differences
title_full_unstemmed A confirmatory factor analysis of the metabolic syndrome in adolescents: an examination of sex and racial/ethnic differences
title_sort confirmatory factor analysis of the metabolic syndrome in adolescents: an examination of sex and racial/ethnic differences
publisher BMC
series Cardiovascular Diabetology
issn 1475-2840
publishDate 2012-10-01
description <p>Abstract</p> <p>Objective</p> <p>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.</p> <p>Research Design and Methods</p> <p>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.</p> <p>Results</p> <p>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.</p> <p>Conclusions</p> <p>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.</p>
topic Metabolic syndrome
Factor analysis, Statistical
Insulin resistance
Pediatrics
Adolescents
Epidemiology
Clinical studies
Obesity
Risk factors
url http://www.cardiab.com/content/11/1/128
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