Erkan Erkan, Muslumanoglu Ahmet Yaser, Oktar Tayfun, Sanli Oner, Ozbek Uğur, Kadioglu Ates
Department of Urology, Haseki Teaching and Research Hospital, Istanbul, Turkey.
J Sex Med. 2006 Jan;3(1):69-75; discussion 75-6. doi: 10.1111/j.1743-6109.2005.00165.x.
Endothelial-derived nitric oxide (NO), which is produced by endothelial nitric oxide synthase (eNOS) in response to increased blood flow, maintains the tumescence phase of erection. The eNOS gene is located on the seventh somatic chromosome and the polymorphism of this gene has been reported to cause changes in the structure of enzyme system, resulting in disturbance of its activity.
The aim of this prospective study is to evaluate the relationship between polymorphism of eNOS gene and erectile dysfunction (ED).
Thirty patients with ED (mean age: 58.7 +/- 9.97, range: 39-74 years) and 25 voluntary controls (mean age: 56.44 +/- 7.58, range: 47-72 years) were enrolled to the study. Patients with ED were evaluated with International Index of Erectile Function (IIEF) questionnaire, routine blood tests for systemic vascular risk factors, and color Doppler ultrasonography while potency of the control group were only assessed with IIEF questionnaire. The presence of polymorphism of eNOS gene was determined in both groups by polymerase chain reaction in the fourth intron of the seventh somatic chromosome that encodes eNOS gene.
The incidences of diabetes mellitus and coronary artery disease were statistically higher in the ED group (P = 0.023 and 0.029, respectively) while mean IIEF score was significantly lower (P = 0.001). Evaluation with color Doppler ultrasonography revealed penile arterial insufficiency in six cases, cavernosal insufficiency in 19 cases, and mixed vascular insufficiency in five cases. The distributions of three eNOS genotypes (eNOS4b/b, eNOS4a/b, and eNOS4a/a) among ED patients and controls were similar (P > 0.05). However, eNOS4a/b genotype was statistically higher in diabetics (P = 0.042). Also, 80% of the patients with severe ED and 54.5% of the diabetic patients with ED had eNOS4a/b genotype.
In our study, no correlation was detected between the polymorphism of eNOS gene and ED. However, 80% of the patients with severe ED and 54.5% of the diabetic patients with ED had eNOS4a/b genotype. Based on our data, it seems that diabetic patients with ED tend to have more eNOS4a/b genotype.
内皮衍生的一氧化氮(NO)由内皮型一氧化氮合酶(eNOS)在血流增加时产生,维持勃起的肿胀期。eNOS基因位于第7号常染色体上,据报道该基因的多态性会导致酶系统结构改变,进而导致其活性紊乱。
本前瞻性研究旨在评估eNOS基因多态性与勃起功能障碍(ED)之间的关系。
30例ED患者(平均年龄:58.7±9.97岁,范围:39 - 74岁)和25名自愿对照者(平均年龄:56.44±7.58岁,范围:47 - 72岁)纳入研究。ED患者采用国际勃起功能指数(IIEF)问卷、全身性血管危险因素的常规血液检查以及彩色多普勒超声进行评估,而对照组仅通过IIEF问卷评估性功能。通过聚合酶链反应在编码eNOS基因的第7号常染色体的第4内含子中测定两组中eNOS基因多态性的存在情况。
ED组糖尿病和冠状动脉疾病的发生率在统计学上更高(分别为P = 0.023和0.029),而平均IIEF评分显著更低(P = 0.001)。彩色多普勒超声评估显示6例阴茎动脉供血不足,19例海绵体供血不足,5例混合性血管供血不足。ED患者和对照组中三种eNOS基因型(eNOS4b/b、eNOS4a/b和eNOS4a/a)的分布相似(P > 0.05)。然而,糖尿病患者中eNOS4a/b基因型在统计学上更高(P = 0.042)。此外,80%的重度ED患者和54.5%的糖尿病ED患者具有eNOS4a/b基因型。
在我们的研究中,未检测到eNOS基因多态性与ED之间的相关性。然而,80%的重度ED患者和54.5%的糖尿病ED患者具有eNOS4a/b基因型。根据我们的数据,似乎糖尿病ED患者倾向于具有更多的eNOS4a/b基因型。