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早年接受冠状动脉造影术患者家庭中血浆载脂蛋白B水平的遗传情况。

Inheritance of plasma apolipoprotein B levels in families of patients undergoing coronary arteriography at an early age.

作者信息

Coresh J, Beaty T H, Kwiterovich P O

机构信息

Welch Center for Prevention, Epidemiology & Clinical Research, Department of Epidemiology, Johns Hopkins Medical Institutions, Baltimore, Maryland 21287-6231.

出版信息

Genet Epidemiol. 1993;10(3):159-76. doi: 10.1002/gepi.1370100303.

DOI:10.1002/gepi.1370100303
PMID:8349099
Abstract

An elevated plasma level of apolipoprotein B (apoB), the major protein of low density lipoproteins, is a risk factor for coronary artery disease. This study tested the hypothesis, suggested by previous studies, that the apoB level is strongly influenced by a major gene. The study population included 832 family members of 116 subjects who had undergone elective coronary arteriography at an early age. The apoB level was adjusted for age, gender, body mass index, alcohol consumption, and cigarette smoking (R2 = 20%). ApoB levels revealed strong familial aggregation with correlations among spouses of 0.23, parent-offspring of 0.16, and siblings of 0.21. Regressive models were used to examine inter-individual variation in adjusted apoB levels. In the total sample, familial aggregation of the apoB level was consistent with two models: (1) a major gene model and (2) a polygenic model with a mixture of non-transmitted "types". Comparison of these two models in each family showed that 57 families supported the first model over the second. Segregation analysis in these 57 families conclusively favored a major gene model with codominant transmission. Genotypic means were 124, 164, and 208 mg/dl with relative frequencies of 45%, 44%, and 11%. Linkage studies in these families can be used to clarify the molecular basis of apoB regulation. However, in the whole population the genetic control of apoB levels may be quite complex.

摘要

载脂蛋白B(apoB)是低密度脂蛋白的主要蛋白质,血浆中apoB水平升高是冠状动脉疾病的一个危险因素。本研究检验了先前研究提出的一个假设,即apoB水平受一个主要基因的强烈影响。研究人群包括116名在早年接受选择性冠状动脉造影的受试者的832名家庭成员。对apoB水平进行了年龄、性别、体重指数、饮酒量和吸烟情况的校正(R2 = 20%)。apoB水平显示出强烈的家族聚集性,配偶间的相关性为0.23,亲子间为0.16,兄弟姐妹间为0.21。使用回归模型来检验校正后apoB水平的个体间差异。在整个样本中,apoB水平的家族聚集性与两种模型一致:(1)一个主要基因模型和(2)一个具有非传递“类型”混合的多基因模型。在每个家庭中对这两种模型进行比较,结果显示57个家庭支持第一种模型而非第二种模型。对这57个家庭进行的分离分析最终支持一个具有共显性传递的主要基因模型。基因型均值分别为124、164和208mg/dl,相对频率分别为45%、44%和11%。对这些家庭进行的连锁研究可用于阐明apoB调控的分子基础。然而,在整个人口中,apoB水平的遗传控制可能相当复杂。

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引用本文的文献

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Genetic epidemiological approaches in the study of risk factors for cardiovascular disease.心血管疾病危险因素研究中的遗传流行病学方法。
Eur J Epidemiol. 2004;19(3):209-17. doi: 10.1023/b:ejep.0000020399.19615.6c.
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A common genetic mechanism determines plasma apolipoprotein B levels and dense LDL subfraction distribution in familial combined hyperlipidemia.
一种常见的遗传机制决定了家族性混合性高脂血症患者的血浆载脂蛋白B水平和致密低密度脂蛋白亚组分分布。
Am J Hum Genet. 1998 Aug;63(2):586-94. doi: 10.1086/301962.
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Inherited susceptibility determines the distribution of dense low-density lipoprotein subfraction profiles in familial combined hyperlipidemia.遗传易感性决定了家族性混合性高脂血症中致密低密度脂蛋白亚组分谱的分布。
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