Center for Human Genome Variation, School of Medicine, Duke University, Durham, North Carolina 27708, USA.
AIDS. 2011 Feb 20;25(4):513-8. doi: 10.1097/QAD.0b013e328343817b.
To date, CCR5 variants remain the only human genetic factors to be confirmed to impact HIV-1 acquisition. However, protective CCR5 variants are largely absent in African populations, in which sporadic resistance to HIV-1 infection is still unexplained. We investigated whether common genetic variants associate with HIV-1 susceptibility in Africans.
We performed a genome-wide association study (GWAS) in a population of 1532 individuals from Malawi, a country with high prevalence of HIV-1 infection. Using single-nucleotide polymorphisms (SNPs) present on the genome-wide chip, we also investigated previously reported associations with HIV-1 susceptibility or acquisition. Recruitment was coordinated by the Center for HIV/AIDS Vaccine Immunology at two sexually transmitted infection clinics. HIV status was determined by HIV rapid tests and nucleic acid testing.
After quality control, the population consisted of 848 high-risk seronegative and 531 HIV-1 seropositive individuals. Logistic regression testing in an additive genetic model was performed for SNPs that passed quality control. No single SNP yielded a significant P value after correction for multiple testing. The study was sufficiently powered to detect markers with genotype relative risk 2.0 or more and minor allele frequencies 12% or more.
This is the first GWAS of host determinants of HIV-1 susceptibility, performed in an African population. The absence of any significant association can have many possible explanations: rarer genetic variants or common variants with weaker effect could be responsible for the resistance phenotype; alternatively, resistance to HIV-1 infection might be due to nongenetic parameters or to complex interactions between genes, immunity and environment.
迄今为止,趋化因子受体 5(CCR5)变异仍然是唯一被证实可影响人类免疫缺陷病毒 1 (HIV-1)获得性感染的遗传因素。然而,在非洲人群中,保护性 CCR5 变异体大多缺失,而这些人群中 HIV-1 感染的散发性抵抗力仍无法解释。我们研究了常见的遗传变异是否与非洲人的 HIV-1 易感性相关。
我们对来自马拉维的 1532 名个体进行了全基因组关联研究(GWAS),该国家 HIV-1 感染率较高。利用全基因组芯片上存在的单核苷酸多态性(SNP),我们还研究了与 HIV-1 易感性或获得性相关的先前报道的关联。该研究由性传播感染诊所的 HIV 艾滋病疫苗免疫中心协调招募。HIV 状态通过 HIV 快速检测和核酸检测确定。
经过质量控制后,该人群由 848 名高危血清阴性和 531 名 HIV-1 血清阳性个体组成。对通过质量控制的 SNP 进行加性遗传模型的逻辑回归检验。经过多重检验校正后,没有单个 SNP 产生显著的 P 值。该研究具有足够的效力来检测基因型相对风险为 2.0 或更高且次要等位基因频率为 12%或更高的标记。
这是在非洲人群中进行的 HIV-1 易感性宿主决定因素的首次全基因组关联研究。没有任何显著关联可能有多种解释:可能是更罕见的遗传变异或效应较弱的常见变异导致了耐药表型;或者,对 HIV-1 感染的抵抗力可能归因于非遗传参数或基因、免疫和环境之间的复杂相互作用。