Recognition and Management of Dyslipidemia in Children and Adolescents

被引:126
|
作者
Kwiterovich, Peter O., Jr. [1 ,2 ]
机构
[1] Johns Hopkins Med Inst, Dept Pediat, Lipid Res Atherosclerosis Div, Baltimore, MD 21205 USA
[2] Johns Hopkins Med Inst, Dept Med, Lipid Res Atherosclerosis Div, Baltimore, MD 21205 USA
来源
关键词
D O I
10.1210/jc.2008-1270
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context: Cardiovascular disease (CVD) remains the number one cause of death in the United States. The origins of atherosclerosis and CVD begin in childhood. Dyslipidemia and obesity are endemic in American youth and require urgent action. Evidence Acquisition: A detailed literature search from 1985-2008 was performed using PubMed and subsequent reference searches of retrieved articles. Selection of included articles was based on rigor of scientific design, adequate sample size, quality of the data, statistical analysis, and hypothesis testing. Evidence Synthesis: CVD risk factors in children predict pathological lesions of atherosclerosis in young adults, and their clinical manifestations, as judged by carotid intima medial thickness, coronary artery calcium, or brachial flow-mediated dilatation. About half the offspring of a parent with premature CVD have a primary dyslipidemia. However, use of family history to identify such youth will miss the majority of children with dyslipidemia. Treatment of dyslipidemia starts with a low-fat diet supplemented with water-soluble fiber, plant stanols, and plant sterols, weight control, and exercise. Drug therapy with inhibitors of hydroxymethylglutaryl coenzyme A reductase, bile acid sequestrants (BAS), and cholesterol absorption inhibitors can be considered in adolescents with a positive family history of premature CVD and a low-density lipoprotein cholesterol of more than 160 mg/dL. Such dietary and drug therapy appears safe and efficacious and is likely to retard atherosclerosis. Conclusions: Early identification and treatment of youth at risk for early atherosclerosis will require an integrated assessment of predisposing CVD risk factors and a comprehensive universal screening and treatment program. (J Clin Endocrinol Metab 93: 4200-4209, 2008)
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页码:4200 / 4209
页数:10
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