Associations between salivary testosterone levels, androgen-related genetic polymorphisms, and self-estimated ejaculation latency time

A1 Originalartikel i en vetenskaplig tidskrift (referentgranskad)


Interna författare/redaktörer


Publikationens författare: Patrick Jern, Lars Westberg, Carina Ankarberg-Lindgren, Ada Johansson, Annika Gunst, N. Kenneth Sandnabba, Pekka Santtila
Förläggare: Wiley-Blackwell
Publiceringsår: 2014
Tidskrift: Sexual Medicine
Volym: 2
Nummer: 3
Artikelns första sida, sidnummer: 107
Artikelns sista sida, sidnummer: 114


Abstrakt

Introduction

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.





Aim

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.





Materials and Methods

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.





Main Outcome Measures

Ejaculatory function was assessed using self-reported ELT.





Results

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.




Conclusions
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.

Senast uppdaterad 2019-19-10 vid 04:33