Hubacek Jaroslav A, Bloudickova Silvie, Kubinova Ruzena, Pikhart Hynek, Viklicky Ondrej, Bobak Martin
Institute for Clinical and Experimental Medicine, CEM, Laboratory for Molecular Genetics, Videnska 1958/9, Prague 4 14021, Czech Republic.
Biochem Genet. 2009 Oct;47(9-10):688-93. doi: 10.1007/s10528-009-9266-y. Epub 2009 Jun 30.
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.
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。