Lu Jiapeng, Sheng Aijuan, Wang Youxin, Zhang Ling, Wu Jingjing, Song Manshu, He Yan, Yu Xinwei, Zhao Feifei, Liu Yezhou, Shao Shuang, Lan Jie, Wu Hao, Wang Wei
School of Public Health and Family Medicine, Capital Medical University, Beijing, China.
Genet Test Mol Biomarkers. 2012 Dec;16(12):1369-75. doi: 10.1089/gtmb.2012.0235. Epub 2012 Oct 11.
The outcome of human immunodeficiency virus (HIV)-1 infection and course to AIDS are variable among individuals. Both chemokine receptor 5 (CCR5) and CCR2 gene polymorphisms play essential roles in the susceptibility of HIV-1 infection. To investigate the main and epistatic effects of the CCR5 promoter and CCR2-V64I polymorphisms on HIV-1 infection in the Northern Han Chinese, subjects of 91 HIV-1-infected patients and 91 health controls were recruited. Single-nucleotide polymorphisms (SNPs) in the CCR5 promoter region and CCR2-V64I variants were genotyped. In the single-locus analysis, CCR5 58755-G and CCR5 59653-T alleles were significantly associated with HIV-1 infection (odds ratio [OR]=0.529, 95% confidence interval [CI]: 0.295-0.948; OR=1.710, 95% CI: 1.039-2.814). After adjustment with age and gender, subjects with the CCR5 59653-CT genotype showed the increased risk of HIV-1 infection compared with those with the wild-type CC genotype (adjusted OR=2.502; 95% CI: 1.332-4.698). No positive association was observed in other SNPs. Haplotype-based association analysis revealed that the haplotype TATGC was associated with the susceptibility to HIV-1 infection (p=0.003). Besides, we found the significant epistatic effects between the CCR5 58755-A/G and CCR5 59029-A/G polymorphisms associated with the lower risk of HIV-1 infection. In addition, we also identified the best three-factor interaction model, including the CCR5 58755-A/G, 59029-A/G, and CCR2-V64I polymorphisms, indicating that there were also strong gene-gene interactions between the CCR5 promoter and CCR2 polymorphisms on the susceptibility of HIV-1 infection. These findings contribute to understanding the genetic mechanism for the susceptibility of HIV-1 infection in Northern Han Chinese.
人类免疫缺陷病毒1型(HIV-1)感染的结果以及发展为艾滋病的病程在个体间存在差异。趋化因子受体5(CCR5)和CCR2基因多态性在HIV-1感染易感性中均起重要作用。为研究CCR5启动子和CCR2-V64I多态性对中国北方汉族人群HIV-1感染的主要及上位效应,招募了91例HIV-1感染患者和91名健康对照者。对CCR5启动子区域的单核苷酸多态性(SNP)和CCR2-V64I变异进行基因分型。在单基因座分析中,CCR5 58755-G和CCR5 59653-T等位基因与HIV-1感染显著相关(优势比[OR]=0.529,95%置信区间[CI]:0.295-0.948;OR=1.710,95%CI:1.039-2.814)。在对年龄和性别进行校正后,CCR5 59653-CT基因型的受试者与野生型CC基因型受试者相比,HIV-1感染风险增加(校正OR=2.502;95%CI:1.332-4.698)。在其他SNP中未观察到正相关。基于单倍型的关联分析显示,单倍型TATGC与HIV-1感染易感性相关(p=0.003)。此外,我们发现CCR5 58755-A/G和CCR5 59029-A/G多态性之间存在显著的上位效应,与较低的HIV-1感染风险相关。此外,我们还确定了最佳三因素相互作用模型,包括CCR5 58755-A/G、59029-A/G和CCR2-V64I多态性,表明CCR5启动子和CCR2多态性在HIV-1感染易感性方面也存在强烈的基因-基因相互作用。这些发现有助于理解中国北方汉族人群HIV-1感染易感性的遗传机制。