Center for Genetic Epidemiology, Department of Preventive Medicine, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
Department of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA; Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Eur Urol. 2020 Sep;78(3):316-320. doi: 10.1016/j.eururo.2020.04.060. Epub 2020 May 12.
Although men of African ancestry have a high risk of prostate cancer (PCa), no genes or mutations have been identified that contribute to familial clustering of PCa in this population. We investigated whether the African ancestry-specific PCa risk variant at 8q24, rs72725854, is enriched in men with a PCa family history in 9052 cases, 143 cases from high-risk families, and 8595 controls of African ancestry. We found the risk allele to be significantly associated with earlier age at diagnosis, more aggressive disease, and enriched in men with a PCa family history (32% of high-risk familial cases carried the variant vs 23% of cases without a family history and 12% of controls). For cases with two or more first-degree relatives with PCa who had at least one family member diagnosed at age <60 yr, the odds ratios for TA heterozygotes and TT homozygotes were 3.92 (95% confidence interval [CI] = 2.13-7.22) and 33.41 (95% CI = 10.86-102.84), respectively. Among men with a PCa family history, the absolute risk by age 60 yr reached 21% (95% CI = 17-25%) for TA heterozygotes and 38% (95% CI = 13-65%) for TT homozygotes. We estimate that in men of African ancestry, rs72725854 accounts for 32% of the total familial risk explained by all known PCa risk variants. PATIENT SUMMARY: We found that rs72725854, an African ancestry-specific risk variant, is more common in men with a family history of prostate cancer and in those diagnosed with prostate cancer at younger ages. Men of African ancestry may benefit from the knowledge of their carrier status for this genetic risk variant to guide decisions about prostate cancer screening.
尽管非裔男性患前列腺癌(PCa)的风险很高,但尚未发现导致该人群中 PCa 家族聚集的基因或突变。我们研究了非洲裔特有的 8q24 上的 PCa 风险变异 rs72725854 是否在 9052 例病例、143 例高危家族病例和 8595 例非洲裔对照中具有 PCa 家族史的男性中富集。我们发现,风险等位基因与更年轻的诊断年龄、更具侵袭性的疾病显著相关,并且在具有 PCa 家族史的男性中富集(32%的高危家族病例携带该变异,而无家族史的病例为 23%,对照组为 12%)。对于有两个或更多一级亲属患有 PCa 且至少有一个家族成员在 60 岁以下被诊断出患有 PCa 的病例,TA 杂合子和 TT 纯合子的比值比分别为 3.92(95%置信区间 [CI] = 2.13-7.22)和 33.41(95% CI = 10.86-102.84)。在具有 PCa 家族史的男性中,到 60 岁时的绝对风险分别为 TA 杂合子的 21%(95% CI = 17-25%)和 TT 纯合子的 38%(95% CI = 13-65%)。我们估计,在非洲裔男性中,rs72725854 占所有已知 PCa 风险变异解释的家族风险的 32%。患者总结:我们发现,rs72725854 是一种非洲裔特有的风险变异,在有前列腺癌家族史的男性和在较年轻被诊断为前列腺癌的男性中更为常见。非洲裔男性可能受益于了解他们携带这种遗传风险变异的情况,以指导前列腺癌筛查的决策。