Results from a prostate cancer admixture mapping study in African-American men

被引:0
|
作者
Cathryn Hufford Bock
Ann G. Schwartz
Julie J. Ruterbusch
Albert M. Levin
Christine Neslund-Dudas
Susan J. Land
Angela S. Wenzlaff
David Reich
Paul McKeigue
Wei Chen
Elisabeth I. Heath
Isaac J. Powell
Rick A. Kittles
Benjamin A. Rybicki
机构
[1] Wayne State University School of Medicine,Western General Hospital
[2] Karmanos Cancer Institute,undefined
[3] Henry Ford Health System,undefined
[4] Harvard Medical School,undefined
[5] Broad Institute of Harvard and MIT,undefined
[6] University of Edinburgh,undefined
[7] University of Chicago,undefined
来源
Human Genetics | 2009年 / 126卷
关键词
Prostate Cancer Risk; African Ancestry; Prostate Cancer Case; Aggressive Prostate Cancer; Admixture Mapping;
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学科分类号
摘要
There are considerable racial disparities in prostate cancer risk, with a 60% higher incidence rate among African-American (AA) men compared with European-American (EA) men, and a 2.4-fold higher mortality rate in AA men than in EA men. Recently, studies have implicated several African-ancestry associated prostate cancer susceptibility loci on chromosome 8q24. In the current study, we performed admixture mapping in AA men from two independent case–control studies of prostate cancer to confirm the 8q24 ancestry association and also identify other genomic regions that may harbor prostate cancer susceptibility genes. A total of 482 cases and 261 controls were genotyped for 1,509 ancestry informative markers across the genome. The mean estimated individual admixture proportions were 20% European and 80% African. The most significant observed increase in European ancestry occurred at rs2141360 on chromosome 7q31 in both the case-only (P = 0.0000035) and case–control analyses. The most significant observed increase in African ancestry across the genome occurred at a locus on chromosome 5q35 identified by SNPs rs7729084 (case-only analysis P = 0.002), and rs12474977 (case–control analysis P = 0.004), which are separated by 646 kb and were adjacent to one another on the panel. On chromosome 8, rs4367565 was associated with the greatest excess African ancestry in both the case-only and case–control analyses (case-only and case–control P = 0.02), confirming previously reported African-ancestry associations with chromosome 8q24. In conclusion, we confirmed ancestry associations on 8q24, and identified additional ancestry-associated regions potentially harboring prostate cancer susceptibility loci.
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页码:637 / 642
页数:5
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