ABCA1
内科学
内膜中层厚度
先证者
胆固醇
丹吉尔病
内分泌学
杂合子优势
医学
等位基因
冠状动脉疾病
生物
颈动脉
运输机
遗传学
基因
突变
作者
Seung Ho Hong,Ward A. Riley,Jeffrey Rhyne,Gina Friel,Michael Miller
出处
期刊:Clinical Chemistry
[American Association for Clinical Chemistry]
日期:2002-11-01
卷期号:48 (11): 2066-2070
被引量:18
标识
DOI:10.1093/clinchem/48.11.2066
摘要
Low HDL-cholesterol (HDL-C) concentrations are inversely correlated with cardiovascular disease, and previous studies have demonstrated that variants in the ATP-binding cassette transporter, ABCA1, are responsible for a proportion of HDL-C deficiency states. We identified a novel variant in ABCA1 in a kindred with decreased HDL-C. This variant was not identified in >200 chromosomes of healthy individuals. The proband, a heterozygote for G2265T, developed premature coronary artery disease. In addition to low HDL-C, six biological family members heterozygous for the ABCA1 variant exhibited low HDL-C concentrations compared with unaffected family members (0.83 +/- 0.32 vs 1.33 +/- 0.36 mmol/L; P = 0.009). Despite the decreased HDL-C, carotid artery B-mode ultrasound studies failed to reveal increased intima-media thickening in affected individuals compared with age- and sex-matched controls. Although these data extend previous observations that a single defective ABCA1 allele may lead to decreased HDL-C, associated evidence of early atherosclerosis was not confirmed.
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