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载脂蛋白B - 100基因多态性对1948年出生的464名丹麦男性血浆脂质的正常变异有影响。

Polymorphisms in the apolipoprotein B-100 gene contributes to normal variation in plasma lipids in 464 Danish men born in 1948.

作者信息

Hansen P S, Gerdes L U, Klausen I C, Gregersen N, Faergeman O

机构信息

Department of Internal Medicine, Aarhus Amtssygehus University Hospital, Denmark.

出版信息

Hum Genet. 1993 Mar;91(1):45-50. doi: 10.1007/BF00230221.

Abstract

We have studied the possible association of 5 polymorphisms in the apoB gene [a 9-bp insertion/deletion length polymorphism in the signal peptide coding region, XbaI, MspI, and EcoRI restriction fragment length polymorphisms (RFLPs) and a 15-bp variable number of tandem repeats (VNTR) region 3' to the apoB gene] with plasma concentrations of cholesterol, high density lipoprotein cholesterol, triglycerides and apolipoprotein B-100 in 464 randomly selected Danish men born in 1948. The XbaI RFLP and the insertion/deletion length polymorphism were significantly associated with plasma concentration and inter-individual variation of cholesterol and apolipoprotein B-100 (1.77% and 1.37% of sample variance in cholesterol, and 1.4% and 1.39% of sample variance in apoB). The association was particularly strong in men with a body mass index less than 25 kg/m2 (the mean value of the whole cohort) (3.43% and 2.93% of sample variance in cholesterol, and 3.1% and 2.13% of sample variance in apoB). The XbaI RFLP and the insertion/deletion length polymorphism were in strong linkage disequilibrium, explaining why independent associations of these two polymorphisms with cholesterol and apoB could not be established. There were no other associations between apoB gene polymorphisms and lipoprotein components.

摘要

我们研究了载脂蛋白B基因中的5种多态性(信号肽编码区域的9碱基对插入/缺失长度多态性、XbaI、MspI和EcoRI限制性片段长度多态性(RFLP)以及载脂蛋白B基因3'端的15碱基对可变串联重复序列(VNTR)区域)与464名随机选取的1948年出生的丹麦男性血浆中胆固醇、高密度脂蛋白胆固醇、甘油三酯和载脂蛋白B-100浓度之间的可能关联。XbaI RFLP和插入/缺失长度多态性与血浆浓度以及胆固醇和载脂蛋白B-100的个体间差异显著相关(胆固醇样本方差的1.77%和1.37%,载脂蛋白B样本方差的1.4%和1.39%)。在体重指数低于25 kg/m²(整个队列的平均值)的男性中,这种关联尤为强烈(胆固醇样本方差的3.43%和2.93%,载脂蛋白B样本方差的3.1%和2.13%)。XbaI RFLP和插入/缺失长度多态性处于强连锁不平衡状态,这解释了为何无法确定这两种多态性与胆固醇和载脂蛋白B的独立关联。载脂蛋白B基因多态性与脂蛋白成分之间没有其他关联。

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