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Replication of genetic loci for sarcoidosis in US black women: Data from the Black Women's Health Study

机译:美国黑人妇女结节病的基因位点复制:来自黑人妇女健康研究的数据

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In the United States, incidence and mortality from sarcoidosis, a chronic, granulomatous disease, are increased in black women. In data from the Black Women's Health Study, a follow-up of US black women, we assessed two SNPs (rs2076530 and rs9268480) previously identified in the BTNL2 gene (chromosome 6p21), of which rs4424066 and rs3817963 are perfect proxies, to determine if they represent independent signals of disease risk. We also assessed whether local ancestry in four genomic regions previously identified through admixture mapping was associated with sarcoidosis. Finally, we assessed the relation of global percent African ancestry to risk. We conducted a nested case-control study of 486 sarcoidosis cases and 943 age- and geography-matched controls. Both BTNL2 SNPs were associated with risk of sarcoidosis in separate models, but in a combined analysis the increased risk was due to the A-allele of the rs3817963 SNP; each copy of the A-allele was associated with a 40 % increase in risk of sarcoidosis (p = 0.02) and was confirmed by our haplotypic analysis. Local African ancestry around the rs30533 ancestry informative marker at chromosome 5q31 was associated with a 29 % risk reduction (p = 0.01). Therefore, we adjusted our analysis of global African ancestry for number of copies of African alleles in rs30533. Subjects in the highest quintile of percent African ancestry had a 54 % increased risk of sarcoidosis. The present results from a population of African-American women support the role of the BTNL2 gene and the 5q31 locus in the etiology of sarcoidosis, and also demonstrate that percent African ancestry is associated with disease risk.
机译:在美国,黑人妇女结节病(一种慢性肉芽肿病)的发病率和死亡率增加。在来自美国黑人妇女的黑人妇女健康研究的数据中,我们评估了先前在BTNL2基因(染色体6p21)中鉴定的两个SNP(rs2076530和rs9268480),其中rs4424066和rs3817963是完美的代理,以确定是否它们代表疾病风险的独立信号。我们还评估了以前通过混合映射确定的四个基因组区域中的本地血统是否与结节病相关。最后,我们评估了全球非洲血统百分比与风险之间的关系。我们对486例结节病病例和943例年龄和地理位置匹配的对照组进行了嵌套病例对照研究。在单独的模型中,两种BTNL2 SNP均与结节病风险相关,但在综合分析中,风险增加是由于rs3817963 SNP的A等位基因引起的。 A等位基因的每份拷贝都使结节病的风险增加40%(p = 0.02),并已通过我们的单倍型分析得到证实。 5q31染色体上rs30533祖先信息标记附近的非洲祖先与降低29%的风险有关(p = 0.01)。因此,我们针对rs30533中非洲等位基因的拷贝数调整了对全球非洲血统的分析。在非洲血统百分比最高的五分之一人群中,结节病的风险增加了54%。来自非裔美国人妇女群体的当前结果支持BTNL2基因和5q31基因座在结节病病因中的作用,并且还证明非洲血统百分比与疾病风险相关。

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