Genetic Epidemiology Laboratory, QIMR Berghofer Medical Research Institute Herston, Queensland, Australia ; Department of Behavioral Sciences and Philosophy, University of Turku Turku, Finland.
Department of Pharmacology, Sahlgrenska Academy, University of Gothenburg Gothenburg, Sweden.
Sex Med. 2014 Aug;2(3):107-14. doi: 10.1002/sm2.34.
Recently, testosterone (T) has been shown to be associated with premature ejaculation (PE) symptoms in the literature. Furthermore, studies suggest that the etiology of PE is partly under genetic control.
The aim of this study was to reassess findings suggesting an association between testosterone (T) and a key symptom of PE, ejaculation latency time (ELT), as well as exploratively investigating associations between six androgen-related genetic polymorphisms and ELT.
Statistical analyses were performed on a population-based sample of 1,429 Finnish men aged 18-45 years (M = 26.9, SD = 4.7). Genotype information was available for 1,345-1,429 of these (depending on the polymorphism), and salivary T samples were available from 384 men. Two androgen receptor gene-linked, two 5-alpha-reductase type 2-gene-linked, and two sex hormone-binding globuline gene-linked polymorphisms were genotyped.
Ejaculatory function was assessed using self-reported ELT.
We found no association between salivary T levels and ELT. We found a nominally significant association between a 5-alpha-reductase type 2-gene-linked polymorphism (rs2208532) and ELT, but this association did not remain significant after correction for multiple testing. One single nucleotide polymorphism in the sex hormone-binding globulin gene (rs1799941) moderated (significantly after correction for multiple testing) the association between salivary T and ELT, so that A:A genotype carriers had significantly lower salivary T levels as a function of increasing ELT compared with other genotype groups.
We were unable to find support for the hypothesis suggesting an association between T levels and ELT, possibly because of the low number of phenotypically extreme cases (the sample used in the present study was population based). Our results concerning genetic associations should be interpreted with caution until replication studies have been conducted. Jern P, Westberg L, Ankarberg-Lindgren C, Johansson A, Gunst A, Sandnabba NK, and Santtila P. Associations between salivary testosterone levels, androgen-related genetic polymorphisms, and self-estimated ejaculation latency time. Sex Med 2014;2:107-114.
最近的文献表明,睾丸酮(T)与早泄(PE)症状有关。此外,研究表明,PE 的病因部分受遗传控制。
本研究旨在重新评估睾丸酮(T)与 PE 的一个关键症状——射精潜伏期时间(ELT)之间的关联,并探索六种与雄激素相关的遗传多态性与 ELT 之间的关联。
对 1429 名年龄在 18-45 岁的芬兰男性(M=26.9,SD=4.7)进行了基于人群的样本的统计分析。这些人中,有 1345-1429 人(取决于多态性)可获得基因型信息,384 人可获得唾液 T 样本。对两个与雄激素受体基因相关、两个与 5α-还原酶 2 型基因相关、两个与性激素结合球蛋白基因相关的多态性进行了基因分型。
采用自我报告的 ELT 评估射精功能。
我们未发现唾液 T 水平与 ELT 之间存在关联。我们发现 5α-还原酶 2 型基因相关的多态性(rs2208532)与 ELT 之间存在名义上的显著关联,但在进行多次测试校正后,这种关联不再显著。性激素结合球蛋白基因中的一个单核苷酸多态性(rs1799941)显著调节(经多次测试校正后)了唾液 T 与 ELT 之间的关联,因此与其他基因型组相比,A:A 基因型携带者的唾液 T 水平随着 ELT 的增加而显著降低。
我们未能发现支持睾丸酮水平与 ELT 之间存在关联的假设,这可能是由于表型极端病例的数量较少(本研究中使用的样本是基于人群的)。关于遗传关联的结果应谨慎解释,直到进行复制研究为止。Jern P, Westberg L, Ankarberg-Lindgren C, Johansson A, Gunst A, Sandnabba NK, and Santtila P. 唾液睾丸酮水平、与雄激素相关的遗传多态性与自我估计的射精潜伏期时间之间的关联。性医学 2014;2:107-114.