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单核苷酸多态性与非裔美国人慢性淋巴细胞白血病的遗传风险。

Single nucleotide polymorphisms and inherited risk of chronic lymphocytic leukemia among African Americans.

机构信息

Department of Medicine, Duke University, Durham, NC, USA.

出版信息

Blood. 2012 Aug 23;120(8):1687-90. doi: 10.1182/blood-2012-02-408799. Epub 2012 Jun 28.

Abstract

The incidence of chronic lymphocytic leukemia (CLL) is significantly lower in African Americans than whites, but overall survival is inferior. The biologic basis for these observations remains unexplored. We hypothesized that germline genetic predispositions differ between African Americans and whites with CLL and yield inferior clinical outcomes among African Americans. We examined a discovery cohort of 42 African American CLL patients ascertained at Duke University and found that the risk allele frequency of most single nucleotide polymorphisms known to confer risk of development for CLL is significantly lower among African Americans than whites. We then confirmed our results in a distinct cohort of 68 African American patients ascertained by the CLL Research Consortium. These results provide the first evidence supporting differential genetic risk for CLL between African Americans compared with whites. A fuller understanding of differential genetic risk may improve prognostication and therapeutic decision making for all CLL patients.

摘要

慢性淋巴细胞白血病 (CLL) 的发病率在美国非裔中明显低于白种人,但总体存活率较低。这些观察结果的生物学基础仍未得到探索。我们假设,CLL 非裔和白种人之间的种系遗传易感性存在差异,并且导致非裔的临床结果较差。我们研究了在杜克大学确定的 42 名非裔美国 CLL 患者的发现队列,发现大多数已知可导致 CLL 发展风险的单核苷酸多态性的风险等位基因频率在非裔美国人中明显低于白种人。然后,我们在由 CLL 研究联合会确定的另一个 68 名非裔美国患者的队列中证实了我们的结果。这些结果首次提供了支持非裔美国人与白种人之间 CLL 遗传风险差异的证据。更全面地了解遗传风险可能会改善所有 CLL 患者的预后和治疗决策。

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