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胆囊疾病患者载脂蛋白B、载脂蛋白A-I和胆固醇酯转运蛋白基因位点的多态性

Polymorphisms at the apoB, apoA-I, and cholesteryl ester transfer protein gene loci in patients with gallbladder disease.

作者信息

Juvonen T, Savolainen M J, Kairaluoma M I, Lajunen L H, Humphries S E, Kesäniemi Y A

机构信息

Department of Surgery, University of Oulu, Finland.

出版信息

J Lipid Res. 1995 Apr;36(4):804-12.

PMID:7616125
Abstract

Alterations in lipoprotein levels are reported to be related to an increased risk of gallstones. Plasma lipid metabolism is regulated by a number of proteins that are polymorphic in the population. The present research was designed to investigate the association between the polymorphisms of these proteins and the presence of various gallbladder diseases. Restriction fragment length polymorphisms (RFLPs) of apolipoprotein B (XbaI, EcoRI), apolipoprotein A-I (PstI, MspI), and cholesteryl ester transfer protein (CETP) (EcoNI, TaqIA, TaqIB) genes were examined in a series of 210 cholecystectomy patients operated on for symptomatic gallbladder disease and in 92 healthy controls. The patients were categorized into four groups according to the type of gallstones and the presence or absence of cholesterolosis. The distribution of CETP TaqIB polymorphism in the patients with cholesterol gallstones differed significantly from that in the controls, with the B1B1 jects (39.7%) (P = 0.036). The patients with both cholesterol and non-cholesterol stones had lower high density lipoprotein (HDL)-cholesterol levels than the control subjects. However, the most distinct difference was found in the gallstone patients with the B2B2 genotype (P = 0.006). The frequency of the X1X1 genotype of the apolipoprotein B XbaI polymorphism was markedly higher in the patients with acalculous cholesterolosis (48.9%) or cholesterolosis with stones (58.1%) than in the gallstone patients with cholesterol stones (27.2%) or with non-cholesterol stones (34.1%) (P = 0.002). The present data suggest that CETP gene polymorphism may ba associated with cholesterol gallstone disease, probably in combination with some additional factor that reduces the plasma HDL cholesterol concentration, especially in TaqIB B2B2 genotype.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

据报道,脂蛋白水平的改变与胆结石风险增加有关。血浆脂质代谢受多种人群中存在多态性的蛋白质调节。本研究旨在调查这些蛋白质的多态性与各种胆囊疾病之间的关联。在一系列210例因有症状胆囊疾病接受胆囊切除术的患者以及92例健康对照中,检测了载脂蛋白B(XbaI、EcoRI)、载脂蛋白A-I(PstI、MspI)和胆固醇酯转运蛋白(CETP)(EcoNI、TaqIA、TaqIB)基因的限制性片段长度多态性(RFLP)。根据胆结石类型以及是否存在胆固醇沉着症,将患者分为四组。胆固醇结石患者中CETP TaqIB多态性的分布与对照组有显著差异,B1B1基因型患者比例为39.7%(P = 0.036)。有胆固醇结石和非胆固醇结石的患者高密度脂蛋白(HDL)胆固醇水平低于对照受试者。然而,在B2B2基因型的胆结石患者中发现了最明显的差异(P = 0.006)。无结石性胆固醇沉着症(48.9%)或有结石的胆固醇沉着症(58.1%)患者中载脂蛋白B XbaI多态性X1X1基因型的频率明显高于有胆固醇结石(27.2%)或非胆固醇结石(34.1%)的胆结石患者(P = 0.002)。目前的数据表明,CETP基因多态性可能与胆固醇结石病有关,可能与一些降低血浆HDL胆固醇浓度的其他因素共同作用,尤其是在TaqIB B2B2基因型中。(摘要截取自250字)

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