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载脂蛋白B基因3个多态性位点的基因内变异性对多民族亚洲人群血清脂质和脂蛋白的影响。

Effects of intragenic variability at 3 polymorphic sites of the apolipoprotein B gene on serum lipids and lipoproteins in a multiethnic Asian population.

作者信息

Choong M L, Sethi S K, Koay E S

机构信息

Department of Pathology, National University of Singapore, Singapore.

出版信息

Hum Biol. 1999 Jun;71(3):381-97.

PMID:10380374
Abstract

We determined the allelic (X+/X-, M+/M-, and E+/E-) distribution frequencies of the XbaI, MspI, and EcoRI restriction fragment length polymorphisms (RFLPs) in the apolipoprotein B gene in a control group of 374 healthy Chinese, Malays, and Indians and in a hyperlipidemic cohort of 131 Chinese patients. Covariability between the RFLPs and serum lipid, lipoprotein, and apolipoprotein concentrations was also studied. We found a lower frequency (average 0.0829) of the X+ allele and higher frequencies of the E+ (average 0.9452) and M+ (average 0.9772) alleles in our study population compared with frequencies reported in other populations. The 3 polymorphic sites did not contribute to significant variations in lipid levels (p > 0.1 in all cases). Also, there was no significant variation in genotype frequencies between the control subjects and the hyperlipidemic subjects. Despite their relative close proximity within the APOB gene sequence, the 3 polymorphic sites did not show any significant linkage disequilibrium. However, the presence of the X+ cutting site was in linkage disequilibrium with the Del allele of the 5' insertion-deletion polymorphism and the E-allele was in linkage disequilibrium with the 3' VNTR located near the 3' end of the coding region of the APOB gene.

摘要

我们测定了374名健康中国人、马来人和印度人组成的对照组以及131名中国高脂血症患者队列中载脂蛋白B基因XbaI、MspI和EcoRI限制性片段长度多态性(RFLP)的等位基因(X+/X-、M+/M-和E+/E-)分布频率。还研究了RFLP与血清脂质、脂蛋白和载脂蛋白浓度之间的协变性。我们发现,与其他人群报道的频率相比,我们研究人群中X+等位基因的频率较低(平均0.0829),而E+(平均0.9452)和M+(平均0.9772)等位基因的频率较高。这3个多态性位点对脂质水平的显著变化没有贡献(所有情况下p>0.1)。此外,对照组和高脂血症组之间的基因型频率没有显著差异。尽管这3个多态性位点在APOB基因序列中相对接近,但它们之间没有显示出任何显著的连锁不平衡。然而,X+切割位点的存在与5'插入-缺失多态性的Del等位基因存在连锁不平衡,E-等位基因与位于APOB基因编码区3'端附近的3'VNTR存在连锁不平衡。

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