Eltonsi T K, Tawfik T M, Rashed L A, GamalEl Din S F, Mahmoud M A
Dermatology and STDS Department, Faculty of Medicine, Al-Azhar University, Darasah Husain, Cairo, Egypt.
Department of Biochemistry, Kasr Al-Ainy Faculty of Medicine, Cairo University, Cairo, Egypt.
Int J Impot Res. 2017 Nov;29(6):235-239. doi: 10.1038/ijir.2017.29. Epub 2017 Sep 14.
We evaluated the role of dopamine (DA) transporter gene polymorphism in lifelong premature ejaculation (LPE) and its role in determining the response to paroxetine and escitalopram. Eighty consecutive patients and controls were recruited. Sixty of them suffered from LPE. They were divided into two equal groups. One group received paroxetine 20 mg daily for 3 months and the other one received ecistalopram 20 mg daily for 3 months. Their wives were instructed to measure the intra-vaginal ejaculation latency time using stopwatch. Five milliliters of blood was withdrawn from patients and controls for PCR analysis. The present study revealed that the mean ages of the patients and controls were 41.42 and 36.4 years, respectively. The majority of the patients were of (10R/10R) genotypes of the DA transporter gene polymorphism, whereas the controls were of (6R/6R) genotypes and this revealed statistically significant result (P-value=0.001). Both paroxitine and escitalopram significantly delayed ejaculation in the responders (P-values=0.001 and 0.001, respectively). The study revealed significant association between such response and DA transporter gene polymorphism (P-values of fold increase and log FI were 0.019 and 0.010, respectively). To the best of our knowledge, this is the first report to demonstrate a highly significant association between such response and DA transporter gene polymorphism in patients with LPE.
我们评估了多巴胺(DA)转运体基因多态性在终身性早泄(LPE)中的作用及其在决定对帕罗西汀和艾司西酞普兰反应中的作用。连续招募了80名患者和对照。其中60人患有LPE。他们被分为两组,每组人数相等。一组患者每天服用20毫克帕罗西汀,持续3个月,另一组患者每天服用20毫克艾司西酞普兰,持续3个月。指导他们的妻子使用秒表测量阴道内射精潜伏期。从患者和对照中抽取5毫升血液用于PCR分析。本研究显示,患者和对照的平均年龄分别为41.42岁和36.4岁。大多数患者为DA转运体基因多态性的(10R/10R)基因型,而对照为(6R/6R)基因型,这一结果具有统计学意义(P值 = 0.001)。帕罗西汀和艾司西酞普兰均显著延迟了有反应者的射精时间(P值分别为0.001和0.001)。研究显示这种反应与DA转运体基因多态性之间存在显著关联(倍数增加的P值和对数FI的P值分别为0.019和0.010)。据我们所知,这是第一份证明LPE患者的这种反应与DA转运体基因多态性之间存在高度显著关联的报告。