Androgen Receptor Gene CAG Repeat Polymorphism Independently Influences Recovery of Male Sexual Function After Testosterone Replacement Therapy in Postsurgical Hypogonadotropic Hypogonadism. (4th March 2014)

• Record Type: Journal Article
• Authors: Tirabassi, Giacomo; delli, Nicola; Corona, Giovanni; Maggi, Mario; Balercia, Giancarlo
• Is Part Of: Journal of sexual medicine. Volume 11:Number 5(2014:May)
• Page Start: 1302
• Page End: 1308
• Publication Date: 2014-03-04
• Subjects: Sexual disorders -- Periodicals; Sex -- Periodicals; Sexual health -- Periodicals; 616.69005
• DOI: 10.1111/jsm.12493
• Languages: English
• ISSNs: 1743-6095

Abstract

<abstract abstract-type="main"> <title>Abstract</title> <sec id="jsm12493-sec-0001" sec-type="section"> <title>Introduction</title> <p>Few and contradictory studies have evaluated the possible influence of androgen receptor (<italic>AR</italic>) gene CAG repeat polymorphism on male sexual function.</p> </sec> <sec id="jsm12493-sec-0002" sec-type="section"> <title>Aim</title> <p>In this study we evaluated the role of AR gene CAG repeat polymorphism in the recovery of sexual function after testosterone replacement therapy (TRT) in men affected by postsurgical hypogonadotropic hypogonadism, a condition which is often associated with hypopituitarism and in which the sexual benefits of TRT must be distinguished from those of pituitary‐function replacement therapies.</p> </sec> <sec id="jsm12493-sec-0003" sec-type="section"> <title>Methods</title> <p>Fifteen men affected by postsurgical hypogonadotropic hypogonadism were retrospectively assessed before and after TRT.</p> </sec> <sec id="jsm12493-sec-0004" sec-type="section"> <title>Main Outcome Measures</title> <p>Main outcome measures included sexual parameters as assessed by the International Index of Erectile Function questionnaire, levels of pituitary dependent hormones (total testosterone, free T3, free T4, cortisol, insulin‐like growth factor‐1 [IGF‐1], prolactin), and results of genetic analysis (<italic>AR</italic> gene CAG repeat number).</p> </sec> <sec id="jsm12493-sec-0005" sec-type="section"> <title>Results</title> <p>Plasma concentrations of free T3, free T4, cortisol, and prolactin did not vary significantly between the two phases, while testosterone and IGF‐1 increased significantly after TRT. A significant improvement in all sexual parameters studied was found. The number of CAG triplets was negatively and significantly correlated with changes in all the sexual parameters, while opposite correlations were found between changes in sexual parameters and changes in testosterone levels; no correlation of change in IGF1 with change in sexual parameters was reported. On multiple linear regression analysis, after correction for changes in testosterone, nearly all the associations between the number of CAG triplets and changes in sexual parameters were confirmed.</p> </sec> <sec id="jsm12493-sec-0006" sec-type="section"> <title>Conclusions</title> <p>Shorter length <italic>AR</italic> gene CAG repeat number is associated with the recovery of sexual function after TRT in postsurgical male hypogonadotropic hypogonadism, independently of the effects of concomitant pituitary‐replacement therapies. <bold>Tirabassi G, delli Muti N, Corona G, Maggi M, and Balercia G. Androgen receptor gene CAG repeat polymorphism independently influences recovery of male sexual function after testosterone replacement therapy in postsurgical hypogonadotropic hypogonadism. J Sex Med 2014;11:1302–1308.</bold></p> </sec> </abstract>