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血液透析患者和健康对照者的载脂蛋白E多态性

Apolipoprotein E polymorphism in hemodialyzed patients and healthy controls.

作者信息

Hubacek Jaroslav A, Bloudickova Silvie, Kubinova Ruzena, Pikhart Hynek, Viklicky Ondrej, Bobak Martin

机构信息

Institute for Clinical and Experimental Medicine, CEM, Laboratory for Molecular Genetics, Videnska 1958/9, Prague 4 14021, Czech Republic.

出版信息

Biochem Genet. 2009 Oct;47(9-10):688-93. doi: 10.1007/s10528-009-9266-y. Epub 2009 Jun 30.

Abstract

A possible association between end-stage renal disease (ESRD) and apolipoprotein E (APOE) polymorphism was found in some but not all studies. We have analyzed the APOE genotypes in 995 hemodialyzed patients (cases) and a sample of 6242 healthy individuals (controls) in the Czech Republic. There was a statistically significant difference in the frequency of APOE alleles between cases and controls, with more carriers of the APOE2 allele in ESRD patients (15.9%) than in controls (12.2%) (P = 0.005). The odds ratio of ESRD for the APOE2 allele, compared with APOE3E3 homozygotes, was 1.37 (95% confidence interval 1.13-1.67). The strength of the association increased with the time spent on hemodialysis: the odds ratio of all-cause ESRD in patients dialyzed for eight or more years was 1.27 (0.94-1.71), for 1-8 years 1.41 (1.09-1.81), and less than 1 year (nonsurvivors) 1.94 (0.88-4.18). This study suggests that the APOE2 allele is a possible genetic risk factor for all-cause ESRD in Caucasians.

摘要

一些研究发现终末期肾病(ESRD)与载脂蛋白E(APOE)多态性之间可能存在关联,但并非所有研究均如此。我们分析了捷克共和国995例血液透析患者(病例组)和6242名健康个体(对照组)的APOE基因型。病例组和对照组之间APOE等位基因频率存在统计学显著差异,ESRD患者中APOE2等位基因携带者(15.9%)多于对照组(12.2%)(P = 0.005)。与APOE3E3纯合子相比,APOE2等位基因导致ESRD的优势比为1.37(95%置信区间1.13 - 1.67)。这种关联的强度随着血液透析时间的延长而增加:透析8年或更长时间的患者全因ESRD的优势比为1.27(0.94 - 1.71),透析1 - 8年的患者为1.41(1.09 - 1.81),透析少于1年(非存活者)为1.94(0.88 - 4.18)。本研究表明,APOE2等位基因可能是白种人全因ESRD的一个遗传风险因素。

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