Andrology, Sexology & STIs Department, Faculty of Medicine, Cairo University, Giza, Egypt.
Department of Dermatology, Andrology & STIs, Faculty of Medicine, Mansoura University, Mansoura, Egypt.
Sex Med Rev. 2020 Oct;8(4):573-585. doi: 10.1016/j.sxmr.2020.05.005. Epub 2020 Jul 4.
Several treatment strategies are nowadays available for erectile dysfunction (ED) patients. Currently, oral phosphodiesterase type 5 inhibitors (PDE5Is) are the first-line therapy for ED. However, they are effective in all treated cases with variable non-responsiveness. Many factors have been listed for this behavior, but the possibility of gene polymorphisms as an underlying cause has not been systematically investigated.
This review aimed to assess the possible involvement of gene polymorphisms affecting the response to PDE5Is in men with ED.
A systematic review was conducted based on a search of all relevant articles in various electronic sites such as PubMed, Medline Medical Subject Headings, Cochrane Library, Science Direct, Scopus, Embase, CINAHL, and Egyptian Knowledge Bank databases. Keywords used for relevant associations were sexual health, genes, variants, erectile dysfunction, polymorphisms, PDE5Is, and cavernous tissues.
Several studies have been carried out to determine the contribution of different encoded genes to ascertain the association between different genotypes and ED men who were non-responders for PDE5Is. 11 studies were selected for this review. In these studies, 6 investigated eNOS genetic polymorphism with variable outcomes. Only 1 study was carried out for each of the following genetic polymorphisms: phosphodiestrase 5A, G-protein β3 subunit, angiotensin converting enzyme, dimethylarginine dimethylaminohydrolase, arginase, and vascular endothelial growth factor with variable results.
Despite the relative shortage of available studies and the varied methodologies used, most of the research articles demonstrated a significant association between genetic polymorphism and the response to PDE5Is, especially for endothelial nitric oxide synthase polymorphism. The limited number of studies that investigated the possible effect of genetic polymorphism and the response to PDE5Is are challenged by many factors, particularly for the definition of responders and non-responders. This should be a motivating factor for researchers to perform further studies with a standardized methodology to address the influence of genetic variations on the response to PDE5Is. Mostafa T, Hassan A, Alghobary MF, et al. Effect of Genetic Polymorphism on the Response to PDE5 Inhibitors in Patients With Erectile Dysfunction: A Systematic Review and a Critical Appraisal. J Sex Med 2020;8:573-585.
目前,针对勃起功能障碍(ED)患者,有多种治疗策略可供选择。目前,口服磷酸二酯酶 5 抑制剂(PDE5Is)是 ED 的一线治疗药物。然而,它们对所有治疗病例的有效性存在差异,存在不同的无应答情况。许多因素都被列为导致这种情况的原因,但基因多态性作为潜在原因的可能性尚未得到系统研究。
本综述旨在评估基因多态性对 ED 患者对 PDE5Is 反应的可能影响。
基于在 PubMed、Medline Medical Subject Headings、Cochrane Library、Science Direct、Scopus、Embase、CINAHL 和埃及知识库等多个电子网站上搜索所有相关文章,进行了系统综述。用于相关关联的关键词包括性健康、基因、变体、勃起功能障碍、多态性、PDE5Is 和海绵体组织。
已经进行了多项研究来确定不同编码基因的贡献,以确定不同基因型与 PDE5Is 无反应的 ED 男性之间的关联。本综述选择了 11 项研究。在这些研究中,有 6 项研究了 eNOS 遗传多态性,结果各不相同。只有 1 项研究分别针对磷酸二酯酶 5A、G 蛋白 β3 亚单位、血管紧张素转换酶、二甲基精氨酸二甲氨基水解酶、精氨酸酶和血管内皮生长因子的遗传多态性进行了研究,结果各不相同。
尽管可用研究相对较少,且使用的方法多种多样,但大多数研究文章都表明基因多态性与 PDE5Is 反应之间存在显著关联,特别是内皮型一氧化氮合酶多态性。由于许多因素的限制,包括对应答者和无应答者的定义,只有少数研究探讨了遗传多态性和 PDE5Is 反应之间的可能影响。这应该是促使研究人员进一步开展研究的一个因素,研究需要采用标准化的方法来解决遗传变异对 PDE5Is 反应的影响。Mostafa T、Hassan A、Alghobary MF 等。遗传多态性对勃起功能障碍患者对 PDE5I 反应的影响:系统评价和批判性评价。J 性医学 2020;8:573-585。