Gao Lei, Zhao Zhifeng, Guo Fengfu, Liu Yan, Guo Jianhua, Zhao Yang, Wang Zhong
Department of Urinary Surgery, Linyi People's Hospital, Linyi 276000, China.
Department of Urinary Surgery, Linyi Cancer Hospital, Linyi 276000, China.
Asian J Androl. 2017 May-Jun;19(3):330-337. doi: 10.4103/1008-682X.163300.
The purpose of our meta-analysis is to examine the associations between three single nucleotide polymorphisms of endothelial nitric oxide synthase (eNOS) gene, G894T, intron 4 and T-786C, and the risk of erectile dysfunction. An electronic database search was performed to identify case-control studies reporting the association between single nucleotide polymorphisms of eNOS gene and erectile dysfunction. Stringent inclusion and exclusion criteria were employed to select high-quality studies for this meta-analysis. Comprehensive Meta-analysis 2.0 software (Biostat Inc., Englewood, New Jersey, USA) was used for statistical analysis of the data extracted from the selected studies. From the initial 203 articles retrieved from database search, this meta-analysis finally selected 12 high-quality case-control studies that conformed to our inclusion criteria. The 12 studies contained a total of 1962 patients with erectile dysfunction and 1752 healthy controls. The results of our meta-analysis showed that G894T correlated with an increased risk erectile dysfunction under both the allele and dominant models (allele: OR = 1.556, 95% CI = 1.064-2.275, P = 0.023; dominant: OR = 1.613, 95% CI = 1.050-2.476, P = 0.029). A similar association was found between T-786C and erectile dysfunction under the allele model (OR = 1.679, 95% CI = 1.341-2.102, P < 0.001), but not under the dominant model (all P > 0.05). Our meta-analysis showed that the two single nucleotide polymorphisms in eNOS gene, G894T and T-786C, are strongly associated with the risk of erectile dysfunction.
我们进行荟萃分析的目的是研究内皮型一氧化氮合酶(eNOS)基因的三个单核苷酸多态性,即G894T、第4内含子和T-786C,与勃起功能障碍风险之间的关联。通过电子数据库检索来识别报告eNOS基因单核苷酸多态性与勃起功能障碍之间关联的病例对照研究。采用严格的纳入和排除标准来选择高质量的研究进行此项荟萃分析。使用综合荟萃分析2.0软件(美国新泽西州恩格尔伍德市的Biostat公司)对从所选研究中提取的数据进行统计分析。从数据库检索最初获得的203篇文章中,本荟萃分析最终选择了12项符合我们纳入标准的高质量病例对照研究。这12项研究共纳入了1962例勃起功能障碍患者和1752例健康对照。我们的荟萃分析结果显示,在等位基因模型和显性模型下,G894T均与勃起功能障碍风险增加相关(等位基因:OR = 1.556,95% CI = 1.064 - 2.275,P = 0.023;显性:OR = 1.613,95% CI = 1.050 - 2.476,P = 0.029)。在等位基因模型下,T-786C与勃起功能障碍之间也发现了类似的关联(OR = 1.679,95% CI = 1.341 - 2.102,P < 0.001),但在显性模型下未发现关联(所有P > 0.05)。我们的荟萃分析表明,eNOS基因中的两个单核苷酸多态性G894T和T-786C与勃起功能障碍风险密切相关。