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Coronary Artery Calcification in Obese Youth: What Are the Phenotypic and Metabolic Determinants?

Identifieur interne : 005A11 ( Main/Merge ); précédent : 005A10; suivant : 005A12

Coronary Artery Calcification in Obese Youth: What Are the Phenotypic and Metabolic Determinants?

Auteurs : Fida Bacha [États-Unis] ; Daniel Edmundowicz [États-Unis] ; Kim Sutton-Tyrell [États-Unis] ; SOJUNG LEE [États-Unis] ; Hala Tfayli [Liban] ; Silva A. Arslanian [États-Unis]

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RBID : Pascal:14-0235270

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English descriptors

Abstract

OBJECTIVE Obesity in adolescence has been associated with increased risk for coronary heart disease in adulthood. This study evaluated subclinical atherosclerosis in obese youth and the underlying risk factors. RESEARCH DESIGN AND METHODS Ninety obese adolescents (37 normal glucose tolerant, 27 prediabetes, and 26 type 2 diabetes) underwent evaluation of coronary artery calcifications (CACs) by electron beam computed tomography, aortic pulse wave velocity (PWV), carotid intima-media thickness (IMT), lipids, leptin, inflammatory markers, and body composition (DEXA). A total of 68 underwent evaluation of insulin sensitivity (IS) (hyperinsulinemic-euglycemic clamp) and abdominal adiposity (computed tomography). RESULTS A total of 50% had CACs (CAC+: Agatston CAC score ≥1). CAC+ youth had higher BMI, fat mass, and abdominal fat, with no difference in sex, race, IS per fat-free mass (ISFFM), glucose tolerance, PWV, or IMT compared with the CAC- group. PWV was inversely related to IS. In multiple regression analyses with age, race, sex, HbA1c, BMI (or waist circumference), ISFFM, diastolic blood pressure, non-HDL cholesterol, and leptin as independent variables, BMI (or waist) (R2 = 0.41; P = 0.001) was the significant determinant of CAC; leptin (R2 = 0.37; P = 0.034) for PWV; and HbA1c, race, and age (R2 = 0.34; P = 0.02) for IMT. CONCLUSIONS Early in the course of obesity, there is evidence of CAC independent of glycemia. The different biomarkers of subclinical atherosclerosis appear to be differentially modulated, adiposity being the major determinant of CAC, hyperglycemia, age, and race for IMT, and leptin and IS for arterial stiffness. These findings highlight the increased cardiovascular disease risk in obese youth and the need for early interventions to reverse obesity and atherosclerosis.

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Pascal:14-0235270

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<term>Adolescent</term>
<term>Calcification</term>
<term>Coronary artery</term>
<term>Determinant</term>
<term>Endocrinology</term>
<term>Metabolic diseases</term>
<term>Metabolism</term>
<term>Nutrition</term>
<term>Nutritional status</term>
<term>Obesity</term>
<term>Phenotype</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr">
<term>Obésité</term>
<term>Artère coronaire</term>
<term>Calcification</term>
<term>Adolescent</term>
<term>Phénotype</term>
<term>Métabolisme</term>
<term>Déterminant</term>
<term>Endocrinologie</term>
<term>Maladie métabolique</term>
<term>Nutrition</term>
<term>Etat nutritionnel</term>
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<term>Nutrition</term>
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<front>
<div type="abstract" xml:lang="en">OBJECTIVE Obesity in adolescence has been associated with increased risk for coronary heart disease in adulthood. This study evaluated subclinical atherosclerosis in obese youth and the underlying risk factors. RESEARCH DESIGN AND METHODS Ninety obese adolescents (37 normal glucose tolerant, 27 prediabetes, and 26 type 2 diabetes) underwent evaluation of coronary artery calcifications (CACs) by electron beam computed tomography, aortic pulse wave velocity (PWV), carotid intima-media thickness (IMT), lipids, leptin, inflammatory markers, and body composition (DEXA). A total of 68 underwent evaluation of insulin sensitivity (IS) (hyperinsulinemic-euglycemic clamp) and abdominal adiposity (computed tomography). RESULTS A total of 50% had CACs (CAC+: Agatston CAC score ≥1). CAC+ youth had higher BMI, fat mass, and abdominal fat, with no difference in sex, race, IS per fat-free mass (IS
<sub>FFM</sub>
), glucose tolerance, PWV, or IMT compared with the CAC- group. PWV was inversely related to IS. In multiple regression analyses with age, race, sex, HbA
<sub>1c</sub>
, BMI (or waist circumference), IS
<sub>FFM</sub>
, diastolic blood pressure, non-HDL cholesterol, and leptin as independent variables, BMI (or waist) (R
<sup>2 </sup>
= 0.41; P = 0.001) was the significant determinant of CAC; leptin (R
<sup>2</sup>
= 0.37; P = 0.034) for PWV; and HbA
<sub>1c</sub>
, race, and age (R
<sup>2</sup>
= 0.34; P = 0.02) for IMT. CONCLUSIONS Early in the course of obesity, there is evidence of CAC independent of glycemia. The different biomarkers of subclinical atherosclerosis appear to be differentially modulated, adiposity being the major determinant of CAC, hyperglycemia, age, and race for IMT, and leptin and IS for arterial stiffness. These findings highlight the increased cardiovascular disease risk in obese youth and the need for early interventions to reverse obesity and atherosclerosis.</div>
</front>
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<li>États-Unis</li>
</country>
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<li>Texas</li>
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<li>Pittsburgh</li>
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<country name="États-Unis">
<region name="Texas">
<name sortKey="Bacha, Fida" sort="Bacha, Fida" uniqKey="Bacha F" first="Fida" last="Bacha">Fida Bacha</name>
</region>
<name sortKey="Arslanian, Silva A" sort="Arslanian, Silva A" uniqKey="Arslanian S" first="Silva A." last="Arslanian">Silva A. Arslanian</name>
<name sortKey="Arslanian, Silva A" sort="Arslanian, Silva A" uniqKey="Arslanian S" first="Silva A." last="Arslanian">Silva A. Arslanian</name>
<name sortKey="Edmundowicz, Daniel" sort="Edmundowicz, Daniel" uniqKey="Edmundowicz D" first="Daniel" last="Edmundowicz">Daniel Edmundowicz</name>
<name sortKey="Sojung Lee" sort="Sojung Lee" uniqKey="Sojung Lee" last="Sojung Lee">SOJUNG LEE</name>
<name sortKey="Sutton Tyrell, Kim" sort="Sutton Tyrell, Kim" uniqKey="Sutton Tyrell K" first="Kim" last="Sutton-Tyrell">Kim Sutton-Tyrell</name>
</country>
<country name="Liban">
<noRegion>
<name sortKey="Tfayli, Hala" sort="Tfayli, Hala" uniqKey="Tfayli H" first="Hala" last="Tfayli">Hala Tfayli</name>
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