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Betteridge, D., Broome, K., Durrington, P., Hawkins, M., Humphries, S., Mann, J., et al. (1999) Mortality in Treated Heterozygous Familial Hypercholesterolaemia: Implications for Clinical Management. Atherosclerosis, 142, 105-112.
https://doi.org/10.1016/S0021-9150(98)00200-7

has been cited by the following article:

• TITLE: A Review of Pediatric Cardiovascular Risk Factors and Current Guidelines

  AUTHORS: Deeksha Sarma, Lawrence M. Benedict, Achintya Moulick, Randy Stevens, Vicki Mahan

  KEYWORDS: Cardiovascular Disease, Familial Hypercholesterolemia, Dyslipidemia, Atherosclerosis

  JOURNAL NAME: World Journal of Cardiovascular Surgery, Vol.8 No.4, April 30, 2018

  ABSTRACT: Dyslipidemia is a highly prevalent condition, and includes a collection of diseases that cause increased levels of plasma triglycerides and/or cholestrol, or decreased levels of HDL-C, with a prototypical disease being familial hypercholesterolemia. Dyslipidemic conditions promote increased atherogenesis through the oxidation of lipids by macrophages, and an increased response to injury by the vascular endothelium. This vascular damage, loss of vascular compliance, and overall hardening of arteries lead to sequellae such as cardiovascular disease, cerebrovascular events, and aneurysm formation. It has been established that certain risk factors predispose individuals to the sequellae of atherosclerosis, including smoking, diabetes, hypertension, and hyperlipidemia. However, studies show that these risk factors can be seen in children as well. This review aims to assess the effect of these risk factors and demonstrate their effects through adolescence into adulthood.