Department of Urology, Huashan Hospital, Fudan University, Shanghai, PR China.
Prostate. 2012 Apr;72(5):577-83. doi: 10.1002/pros.21462. Epub 2011 Jul 27.
Genome-wide association studies (GWAS) have identified more than 30 single nucleotide polymorphisms (SNPs) that were reproducibly associated with prostate cancer (PCa) risk in populations of European descent. In aggregate, these variants have shown potential to predict risk for PCa in European men. However, their utility for PCa risk prediction in Chinese men is unknown.
We selected 33 PCa risk-related SNPs that were originally identified in populations of European descent. Genetic scores were estimated for subjects in a Chinese case-control study (1,108 cases and 1,525 controls) based on these SNPs. To assess the performance of the genetic score on its ability to predict risk for PCa, we calculated area under the curve (AUC) of the receiver operating characteristic (ROC) in combination with 10-fold cross-validation.
The genetic score was significantly higher for cases than controls (P = 5.91 × 10(-20)), and was significantly associated with risk of PCa in a dose-dependent manner (P for trend: 4.78 × 10(-18)). The AUC of the genetic score was 0.604 for risk prediction of PCa in Chinese men. When ORs derived from this Chinese study population were used to calculate genetic score, the AUCs were 0.631 for all 33 SNPs and 0.617 when using only the 11 significant SNPs.
Our results indicate that genetic variants related to PCa risk may be useful for risk prediction in Chinese men. Prospective studies are warranted to further evaluate these findings.
全基因组关联研究(GWAS)已经确定了 30 多个单核苷酸多态性(SNP),这些 SNP 在欧洲血统的人群中与前列腺癌(PCa)风险具有可重复性关联。总体而言,这些变体显示出了在欧洲男性中预测 PCa 风险的潜力。然而,它们在中国男性中预测 PCa 风险的效用尚不清楚。
我们选择了 33 个最初在欧洲人群中确定的与 PCa 风险相关的 SNP。根据这些 SNP,我们基于中国病例对照研究(1108 例病例和 1525 例对照)中的受试者估计了 PCa 风险相关的遗传评分。为了评估遗传评分预测 PCa 风险的性能,我们计算了接收者操作特征(ROC)曲线下面积(AUC)并结合了 10 倍交叉验证。
病例组的遗传评分明显高于对照组(P = 5.91 × 10(-20)),并且与 PCa 风险呈剂量依赖性相关(趋势检验 P = 4.78 × 10(-18))。遗传评分对中国男性 PCa 风险的预测 AUC 为 0.604。当使用来自中国研究人群的 OR 来计算遗传评分时,33 个 SNP 的 AUC 为 0.631,仅使用 11 个有意义的 SNP 的 AUC 为 0.617。
我们的结果表明,与 PCa 风险相关的遗传变异可能对中国男性的风险预测有用。需要前瞻性研究来进一步评估这些发现。