Department of Urology, First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, China.
Asian J Androl. 2012 Jul;14(4):560-5. doi: 10.1038/aja.2012.4. Epub 2012 Apr 16.
To derive a precise estimation of the associations between the cytochrome P450 1B1 (CYP1B1) 4326C/G variants and prostate cancer (PCa) risk or aggressiveness, a meta-analysis was performed using all eligible published studies. Odds ratios (ORs) with 95% confidence intervals (CIs) were estimated to assess the association in seven literature studies with 2788 cases and 2968 controls. In the overall analysis, no significant association was found between the CYP1B1 4326C/G polymorphism and PCa risk, but ethnicity subgroup analyses and a case-source analysis revealed significant associations. The 4326G allele showed a significant association with increased PCa risk in Asians (OR=1.52, 95% CI: 1.20-1.92), and significant associations were also observed in a heterozygote comparison (OR=1.40, 95% CI: 1.03-1.89), a homozygote comparison (OR=2.38, 95% CI: 1.31-4.33) and in a dominant genetic model (OR=1.52, 95% CI: 1.14-2.01). Moreover, the 4326G allele was also significantly correlated with an increased risk of sporadic PCa (OR=1.13, 95% CI: 1.04-1.24), and significant associations were observed in a heterozygote comparison (OR=1.16, 95% CI: 1.02-1.33), a homozygote comparison (OR=1.24, 95% CI: 1.03-1.49) and a dominant genetic model (OR=1.19, 95% CI: 1.05-1.34). The overall analyses and all subgroup analyses showed no significant association between the 4326C/G polymorphism and PCa aggressiveness. Our meta-analysis showed that CYP1B1 4326G allele is significantly associated with an increased PCa risk in Asians and in sporadic PCa cases.
为了精确评估细胞色素 P450 1B1(CYP1B1)4326C/G 变体与前列腺癌(PCa)风险或侵袭性之间的关联,我们对所有符合条件的已发表研究进行了荟萃分析。使用比值比(OR)和 95%置信区间(CI)来评估 7 项文献研究中 2788 例病例和 2968 例对照的相关性。在总体分析中,CYP1B1 4326C/G 多态性与 PCa 风险之间没有显著关联,但亚组分析和病例来源分析显示存在显著关联。4326G 等位基因与亚洲人群 PCa 风险增加显著相关(OR=1.52,95%CI:1.20-1.92),在杂合子比较(OR=1.40,95%CI:1.03-1.89)、纯合子比较(OR=2.38,95%CI:1.31-4.33)和显性遗传模型(OR=1.52,95%CI:1.14-2.01)中也观察到显著关联。此外,4326G 等位基因还与散发性 PCa 风险增加显著相关(OR=1.13,95%CI:1.04-1.24),在杂合子比较(OR=1.16,95%CI:1.02-1.33)、纯合子比较(OR=1.24,95%CI:1.03-1.49)和显性遗传模型(OR=1.19,95%CI:1.05-1.34)中也观察到显著关联。总体分析和所有亚组分析均显示,CYP1B1 4326C/G 多态性与 PCa 侵袭性之间无显著关联。本荟萃分析表明,CYP1B1 4326G 等位基因与亚洲人群和散发性 PCa 病例的 PCa 风险增加显著相关。