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Variant Discovery and Fine Mapping of Genetic Loci Associated with Blood Pressure Traits in Hispanics and African Americans

机译:西班牙裔美国人和非裔美国人与血压特征相关的基因座的变异发现和精细定位

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摘要

Despite the substantial burden of hypertension in US minority populations, few genetic studies of blood pressure have been conducted in Hispanics and African Americans, and it is unclear whether many of the established loci identified in European-descent populations contribute to blood pressure variation in non-European descent populations. Using the Metabochip array, we sought to characterize the genetic architecture of previously identified blood pressure loci, and identify novel cardiometabolic variants related to systolic and diastolic blood pressure in a multi-ethnic US population including Hispanics (n = 19,706) and African Americans (n = 18,744). Several known blood pressure loci replicated in African Americans and Hispanics. Fourteen variants in three loci (KCNK3, FGF5, ATXN2-SH2B3) were significantly associated with blood pressure in Hispanics. The most significant diastolic blood pressure variant identified in our analysis, rs2586886/KCNK3 (P = 5.2 x 10−9), also replicated in independent Hispanic and European-descent samples. African American and trans-ethnic meta-analysis data identified novel variants in the FGF5, ULK4 and HOXA-EVX1 loci, which have not been previously associated with blood pressure traits. Our identification and independent replication of variants in KCNK3, a gene implicated in primary hyperaldosteronism, as well as a variant in HOTTIP (HOXA-EVX1) suggest that further work to clarify the roles of these genes may be warranted. Overall, our findings suggest that loci identified in European descent populations also contribute to blood pressure variation in diverse populations including Hispanics and African Americans—populations that are understudied for hypertension genetic risk factors.
机译:尽管在美国少数民族人群中高血压负担沉重,但在西班牙裔和非裔美国人中进行的血压遗传学研究很少,目前尚不清楚在欧洲血统人群中确定的许多已确定的基因座是否会导致非欧洲人后裔。使用Metabochip阵列,我们试图表征先前确定的血压位点的遗传结构,并鉴定与多族裔美国人口(包括西班牙裔(n = 19,706)和非洲裔美国人(n))有关的收缩压和舒张压的新的心脏代谢变异。 = 18744)。在非裔美国人和西班牙裔中复制了几个已知的血压位点。三个位点(KCNK3,FGF5,ATXN2-SH2B3)中的14个变异与西班牙裔患者的血压显着相关。我们分析中发现的最重要的舒张压变异体rs2586886 / KCNK3(P = 5.2 x 10 −9 )也可以在独立的西班牙裔和欧洲裔样本中复制。非裔美国人和跨种族的荟萃分析数据确定了FGF5,ULK4和HOXA-EVX1基因座中的新变异,这些变异先前并未与血压特征相关联。我们对KCNK3(与原发性醛固酮增多症有关的基因)以及HOTTIP(HOXA-EVX1)的变异体中的变异体的鉴定和独立复制表明,可能有必要开展进一步工作来阐明这些基因的作用。总体而言,我们的发现表明,在欧洲血统人群中鉴定出的基因座也导致包括西班牙裔和非裔美国人在内的各种人群的血压变化,而这些人群的高血压遗传风险因素仍未得到充分研究。

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