Department of Medicine, College of Physicians and Surgeons, Columbia University, New York, New York, United States of America.
PLoS Genet. 2012;8(6):e1002765. doi: 10.1371/journal.pgen.1002765. Epub 2012 Jun 21.
IgA nephropathy (IgAN), major cause of kidney failure worldwide, is common in Asians, moderately prevalent in Europeans, and rare in Africans. It is not known if these differences represent variation in genes, environment, or ascertainment. In a recent GWAS, we localized five IgAN susceptibility loci on Chr.6p21 (HLA-DQB1/DRB1, PSMB9/TAP1, and DPA1/DPB2 loci), Chr.1q32 (CFHR3/R1 locus), and Chr.22q12 (HORMAD2 locus). These IgAN loci are associated with risk of other immune-mediated disorders such as type I diabetes, multiple sclerosis, or inflammatory bowel disease. We tested association of these loci in eight new independent cohorts of Asian, European, and African-American ancestry (N = 4,789), followed by meta-analysis with risk-score modeling in 12 cohorts (N = 10,755) and geospatial analysis in 85 world populations. Four susceptibility loci robustly replicated and all five loci were genome-wide significant in the combined cohort (P = 5×10⁻³²-3×10⁻¹⁰), with heterogeneity detected only at the PSMB9/TAP1 locus (I² = 0.60). Conditional analyses identified two new independent risk alleles within the HLA-DQB1/DRB1 locus, defining multiple risk and protective haplotypes within this interval. We also detected a significant genetic interaction, whereby the odds ratio for the HORMAD2 protective allele was reversed in homozygotes for a CFHR3/R1 deletion (P = 2.5×10⁻⁴). A seven-SNP genetic risk score, which explained 4.7% of overall IgAN risk, increased sharply with Eastward and Northward distance from Africa (r = 0.30, P = 3×10⁻¹²⁸). This model paralleled the known East-West gradient in disease risk. Moreover, the prediction of a South-North axis was confirmed by registry data showing that the prevalence of IgAN-attributable kidney failure is increased in Northern Europe, similar to multiple sclerosis and type I diabetes. Variation at IgAN susceptibility loci correlates with differences in disease prevalence among world populations. These findings inform genetic, biological, and epidemiological investigations of IgAN and permit cross-comparison with other complex traits that share genetic risk loci and geographic patterns with IgAN.
IgA 肾病(IgAN)是全球范围内导致肾衰竭的主要原因,在亚洲人群中较为常见,在欧洲人群中中等流行,在非洲人群中罕见。这些差异是否代表基因、环境或检出率的差异尚不清楚。在最近的一项全基因组关联研究中,我们将 IgAN 易感性位点定位于 6p21(HLA-DQB1/DRB1、PSMB9/TAP1 和 DPA1/DPB2 位点)、1q32(CFHR3/R1 位点)和 22q12(HORMAD2 位点)上。这些 IgAN 位点与其他免疫介导疾病(如 1 型糖尿病、多发性硬化症或炎症性肠病)的风险相关。我们在亚洲、欧洲和非裔美国人的 8 个新独立队列中(N = 4789)进行了这些位点的关联测试,随后在 12 个队列(N = 10755)中进行了风险评分建模的荟萃分析,并在 85 个世界人群中进行了地理空间分析。有 4 个易感位点得到了稳健的复制,在合并队列中所有 5 个位点均达到全基因组显著水平(P = 5×10⁻³²-3×10⁻¹⁰),仅在 PSMB9/TAP1 位点检测到异质性(I² = 0.60)。条件分析在 HLA-DQB1/DRB1 位点内确定了两个新的独立风险等位基因,定义了该区间内多个风险和保护单倍型。我们还检测到一个显著的遗传相互作用,即 HORMAD2 保护等位基因的优势比在 CFHR3/R1 缺失的纯合子中逆转(P = 2.5×10⁻⁴)。一个由 7 个 SNP 组成的遗传风险评分可以解释 4.7%的整体 IgAN 风险,该评分与非洲向东和向北的距离呈显著正相关(r = 0.30,P = 3×10⁻¹²⁸)。该模型与疾病风险的已知东西梯度相吻合。此外,通过登记数据证实了南北轴的预测,该数据表明,北欧 IgAN 相关肾衰竭的患病率增加,类似于多发性硬化症和 1 型糖尿病。IgAN 易感性位点的变异与世界人群中疾病流行率的差异相关。这些发现为 IgAN 的遗传、生物学和流行病学研究提供了信息,并允许与具有 IgAN 遗传风险位点和地理模式的其他复杂特征进行交叉比较。