Brown Lisa A, Sofer Tamar, Stilp Adrienne M, Baier Leslie J, Kramer Holly J, Masindova Ivica, Levy Daniel, Hanson Robert L, Moncrieft Ashley E, Redline Susan, Rosas Sylvia E, Lash James P, Cai Jianwen, Laurie Cathy C, Browning Sharon, Thornton Timothy, Franceschini Nora
Department of Biostatistics, University of Washington School of Public Health, Seattle, Washington.
Epidemiology and Clinical Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Phoenix, Arizona.
J Am Soc Nephrol. 2017 Jul;28(7):2211-2220. doi: 10.1681/ASN.2016091010. Epub 2017 Jan 30.
Increased urine albumin excretion is highly prevalent in Hispanics/Latinos. Previous studies have found an association between urine albumin excretion and Amerindian ancestry in Hispanic/Latino populations. Admixture between racial/ethnic groups creates long-range linkage disequilibrium between variants with different allelic frequencies in the founding populations and it can be used to localize genes. Hispanic/Latino genomes are an admixture of European, African, and Amerindian ancestries. We leveraged this admixture to identify associations between urine albumin excretion (urine albumin-to-creatinine ratio [UACR]) and genomic regions harboring variants with highly differentiated allele frequencies among the ancestral populations. Admixture mapping analysis of 12,212 Hispanic Community Health Study/Study of Latinos participants, using a linear mixed model, identified three novel genome-wide significant signals on chromosomes 2, 11, and 16. The admixture mapping signal identified on chromosome 2, spanning q11.2-14.1 and not previously reported for UACR, is driven by a difference between Amerindian ancestry and the other two ancestries (<5.7 × 10). Within this locus, two common variants located at the proapoptotic gene associated with UACR: rs116907128 (allele frequency =0.14; =1.5 × 10) and rs586283 (C allele frequency =0.35; =4.2 × 10). In a secondary analysis, rs116907128 accounted for most of the admixture mapping signal observed in the region. The rs116907128 variant is common among full-heritage Pima Indians (A allele frequency =0.54) but is monomorphic in the 1000 Genomes European and African populations. In a replication analysis using a sample of full-heritage Pima Indians, rs116907128 significantly associated with UACR (=0.01; =1568). Our findings provide evidence for the presence of Amerindian-specific variants influencing the variation of urine albumin excretion in Hispanics/Latinos.
尿白蛋白排泄增加在西班牙裔/拉丁裔人群中非常普遍。先前的研究发现,西班牙裔/拉丁裔人群中尿白蛋白排泄与美洲印第安人血统之间存在关联。种族/族裔群体之间的混合在创始人群体中具有不同等位基因频率的变异之间产生了长程连锁不平衡,并且可以用于基因定位。西班牙裔/拉丁裔基因组是欧洲、非洲和美洲印第安人血统的混合体。我们利用这种混合来确定尿白蛋白排泄(尿白蛋白与肌酐比值[UACR])与在祖先群体中等位基因频率高度分化的变异所在基因组区域之间的关联。对12212名西班牙裔社区健康研究/拉丁裔研究参与者进行混合映射分析,使用线性混合模型,在2号、11号和16号染色体上确定了三个新的全基因组显著信号。在2号染色体上确定的混合映射信号,跨越q11.2 - 14.1,此前未报道与UACR相关,是由美洲印第安人血统与其他两个血统之间的差异驱动的(<5.7×10)。在这个基因座内,位于促凋亡基因上的两个常见变异与UACR相关:rs116907128(等位基因频率 = 0.14;= 1.5×10)和rs586283(C等位基因频率 = 0.35;= 4.2×10)。在一项二次分析中,rs116907128占该区域观察到的混合映射信号的大部分。rs116907128变异在纯血统皮马印第安人中很常见(A等位基因频率 = 0.54),但在1000基因组计划的欧洲和非洲人群中是单态的。在一项使用纯血统皮马印第安人样本的重复分析中,rs116907128与UACR显著相关(= 0.01;= 1568)。我们的研究结果为存在影响西班牙裔/拉丁裔人群尿白蛋白排泄变异的美洲印第安人特异性变异提供了证据。