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首页> 外文期刊>The American Journal of Human Genetics >Admixture mapping of white cell count: Genetic locus responsible for lower white blood cell count in the health ABC and Jackson Heart Studies
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Admixture mapping of white cell count: Genetic locus responsible for lower white blood cell count in the health ABC and Jackson Heart Studies

机译:白细胞计数的混合图谱:在健康ABC和杰克逊心脏研究中,导致较低白细胞计数的遗传基因座

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摘要

White blood cell count (WBC) is an important clinical marker that varies among different ethnic groups. African Americans are known to have a lower WBC than European Americans. We surveyed the entire genome for loci underlying this difference in WBC by using admixture mapping. We analyzed data from African American participants in the Health, Aging, and Body Composition Study and the Jackson Heart Study. Participants of both studies were genotyped across >= 1322 single nucleotide polymorphisms that were preselected to be informative for African versus European ancestry and span the entire genome. We used these markers to estimate genetic ancestry in each chromosomal region and then tested the association between WBC and genetic ancestry at each locus. We found a locus on chromosome 1q strongly associated with WBC (P < 10(-12)). The strongest association was with a marker known to affect the expression of the Duffy blood group antigen. Participants who had both copies of the common West African allele had a mean WBC of 4.9 (SD 1.3); participants who had both common European alleles had a mean WBC of 7.1 (SD 1.3). This variant explained similar to 20% of population variation in WBC. We used admixture mapping, a novel method for conducting genetic-association studies, to find a region that was significantly associated with WBC on chromosome 1q. Additional studies are needed to determine the biological mechanism for this effect and its clinical implications.
机译:白细胞计数(WBC)是重要的临床标记,在不同种族之间存在差异。非洲裔美国人的WBC低于欧美人。我们通过使用混合作图对整个基因组中WBC差异的潜在位点进行了调查。我们分析了来自非裔美国人参与健康,衰老和身体成分研究以及杰克逊心脏研究的数据。两项研究的参与者均经过了≥= 1322个单核苷酸多态性的基因分型,这些多态性已预先选择为对非洲人和欧洲人有帮助,并涵盖了整个基因组。我们使用这些标记来估计每个染色体区域中的遗传祖先,然后在每个基因座处检验WBC和遗传祖先之间的关联。我们在染色体1q上发现了一个与WBC密切相关的基因座(P <10(-12))。最强的关联是与已知会影响达菲血型抗原表达的标记物相关。拥有西非共同等位基因的两个副本的参与者的平均白细胞数为4.9(标准差1.3);具有欧洲共同等位基因的参与者的平均白细胞为7.1(标准差1.3)。这种变异解释了WBC中人口变异的20%。我们使用混合映射(一种进行遗传关联研究的新方法)来查找与1q号染色体上的WBC显着相关的区域。需要进行其他研究以确定这种作用的生物学机制及其临床意义。

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