alexa Prevalence of dyslipidemia in non-obese prepubertal children and its association with family history of diabetes, high blood pressure, and obesity.
Immunology

Immunology

Journal of Clinical & Cellular Immunology

Author(s): GuerreroRomero F, RodrguezMorn M

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Abstract BACKGROUND: Because obesity masks the need for screening, there is no previous description of dyslipidemia in healthy normal-weight children. The aims of this study were a) to determine the prevalence of disorders in lipid profile among non-obese prepubertal children, and b) to establish its association with the family history (FH) of high blood pressure (HBP), type 2 diabetes (T2-DM), and obesity. METHODS: A random sample of 439 healthy normal-weight children, 218 girls and 221 boys, aged 10-13 years and Tanner stage 1-2 were enrolled in a community-based cross-sectional study carried out in Durango, in northern Mexico. For verifying accuracy of FH, a direct detailed medical history including anthropometric and laboratory measurements was directly obtained from both parents. RESULTS: Among parents, prevalence (95\% CI) of T2-DM, HBP, and obesity was 8.3\% (3.5-14.3), 14.2\% (8.6-24.6), and 28.5\% (24-33), and for hypercholesterolemia, low HDL-cholesterol, high LDL-cholesterol, hypertriglyceridemia, and mixed hyperlipidemia 17.9 \% (15-20), 27.8\% (25-30), 14.3\% (12-16), 32.3\% (29-35), and 9.8 \% (8-12), respectively. Among children, prevalence (95\% CI) for high total cholesterol, low HDL-cholesterol, high LDL-cholesterol, isolated hypertriglyceridemia, and mixed hyperlipidemia was 15.9\% (12.6-19.5); 6.2\% (4.0-8.5); 14.6\% (11.4-18.0); 9.3\% (6.7-12.2); and 3.6\% (2.1-5.8), respectively. Sex- and birth weight-adjusted odds ratio (95\% CI) showed that FH of T2-DM, but not of HBP and obesity, was associated with hypercholesterolemia (2.1; 1.2-6.2), low HDL-cholesterol (1.8; 1.1-5.7), and hypertriglyceridemia (2.3; 1.1-6.4). CONCLUSIONS: Non-obese children in this sample display a high prevalence of abnormalities in lipid profile associated with FH of T2-DM. This article was published in Arch Med Res and referenced in Journal of Clinical & Cellular Immunology

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