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全血细胞性状的 GWAS 分析在白种人和非裔美国儿童中鉴定出新的关联位点和上位性相互作用。

GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children.

机构信息

Center for Applied Genomics, Abramson Research Center and Division of Human Genetics, The Children’s Hospital of Philadelphia, Philadelphia, PA 19104, USA.

出版信息

Hum Mol Genet. 2013 Apr 1;22(7):1457-64. doi: 10.1093/hmg/dds534. Epub 2012 Dec 20.

Abstract

Hematological traits are important clinical indicators, the genetic determinants of which have not been fully investigated. Common measures of hematological traits include red blood cell (RBC) count, hemoglobin concentration (HGB), hematocrit (HCT), mean corpuscular hemoglobin (MCH), MCH concentration (MCHC), mean corpuscular volume (MCV), platelet count (PLT) and white blood cell (WBC) count. We carried out a genome-wide association study of the eight common hematological traits among 7943 African-American children and 6234 Caucasian children. In African Americans, we report five novel associations of HBE1 variants with HCT and MCHC, the alpha-globin gene cluster variants with RBC and MCHC, and a variant at the ARHGEF3 locus with PLT, as well as replication of four previously reported loci at genome-wide significance. In Caucasians, we report a novel association of variants at the COPZ1 locus with PLT as well as replication of four previously reported loci at genome-wide significance. Extended analysis of an association observed between MCH and the alpha-globin gene cluster variants demonstrated independent effects and epistatic interaction at the locus, impacting the risk of iron deficiency anemia in African Americans with specific genotype states. In summary, we extend the understanding of genetic variants underlying hematological traits based on analyses in African-American children.

摘要

血液学特征是重要的临床指标,但其遗传决定因素尚未得到充分研究。常见的血液学特征指标包括红细胞计数(RBC)、血红蛋白浓度(HGB)、血细胞比容(HCT)、平均红细胞血红蛋白量(MCH)、平均红细胞血红蛋白浓度(MCHC)、平均红细胞体积(MCV)、血小板计数(PLT)和白细胞计数(WBC)。我们对 7943 名非裔美国儿童和 6234 名白种人儿童的 8 种常见血液学特征进行了全基因组关联研究。在非裔美国人中,我们报告了 HBE1 变体与 HCT 和 MCHC、α-珠蛋白基因簇变体与 RBC 和 MCHC 以及 ARHGEF3 基因座上的一个变体与 PLT 之间的五个新关联,以及四个以前报道的全基因组显著关联位点的复制。在白种人中,我们报告了 COPZ1 基因座上的变体与 PLT 之间的新关联,以及四个以前报道的全基因组显著关联位点的复制。对 MCH 与α-珠蛋白基因簇变体之间观察到的关联进行的扩展分析表明,该基因座存在独立的影响和上位性相互作用,影响特定基因型状态下非裔美国人缺铁性贫血的风险。总之,我们基于对非裔美国儿童的分析,扩展了对血液学特征遗传变异的理解。

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