|Year : 2014 | Volume
| Issue : 4 | Page : 643
Gene mapping of serotoninergic system polymorphisms provides insight on pathology and treatment of men with lifelong premature ejaculation
Theodore R Saitz1, Ege Can Serefoglu2
1 Department of Urology, Oregon Health and Science University, Portland, Oregon, USA
2 Department of Urology, Bagcilar Training and Research Hospital, Istanbul, Turkey
|Date of Web Publication||29-Apr-2014|
Ege Can Serefoglu
Department of Urology, Bagcilar Training and Research Hospital, Istanbul
Source of Support: None, Conflict of Interest: None
|How to cite this article:|
Saitz TR, Serefoglu EC. Gene mapping of serotoninergic system polymorphisms provides insight on pathology and treatment of men with lifelong premature ejaculation. Asian J Androl 2014;16:643
|How to cite this URL:|
Saitz TR, Serefoglu EC. Gene mapping of serotoninergic system polymorphisms provides insight on pathology and treatment of men with lifelong premature ejaculation. Asian J Androl [serial online] 2014 [cited 2021 Jan 25];16:643. Available from: https://www.ajandrology.com/text.asp?2014/16/4/643/126372 - DOI: 10.4103/1008-682X.126372
In spite of its long history and high prevalence, the exact pathophysiology of premature ejaculation (PE) remains to be unknown.  Over a decade ago, Waldinger et al.  initially suggested that hypersensitivity of 5-HT1A receptors and/or hypofunction of 5-HT2C receptors might be responsible for this phenomenon; thus, the daily use of a selective serotonin reuptake inhibitor has now emerged as an effective treatment for delaying ejaculation.
The study of Janssen et al.  provided further evidence regarding the differences in serotonin receptors in patients with lifelong PE (LPE). Using a similar method, associations of the intravaginal ejaculatory latency time with other various polymorphisms of the serotonergic system have also been found. , The study of Janssen et al.  adds to the hypothesis that apart from these previously discussed polymorphisms, the Cys23Ser 5-HT2C receptor gene polymorphism is associated with the intravaginal ejaculatory latency time in men with LPE.  This opens a floodgate opportunity with regards to further gene mapping of the serotonergic system, with a potential to clinically correlate results.
This exciting study sheds light on the pathophysiology of LPE and we hope that it will serve as a springboard to inspire others to investigate other possible genetic polymorphisms that could be contributing to LPE. As multiple serotonin system genetic polymorphisms have been associated with the increased intravaginal ejaculatory latency time of LPE, ,, it is likely that numerous other polymorphisms of the 5-HT2C-receptor gene will have to be investigated, if we wish to gain complete understanding in the role of the serotonergic system in LPE. Of note, the current study involved a population limited to 94% Caucasian Dutch men. As genetic diversity is common between populations, it may be beneficial to confirm results in various populations, as the authors stated. Additionally, it would be beneficial to conduct similar studies in larger cohorts, as the number of subjects currently studied is low for an epidemiologic genetic study. Nevertheless, the simplicity and elegance of the study should be inspiring to all as we work towards gaining a better understanding of the mechanisms behind LPE, which will ultimately lead to targeted treatments and improved quality of life for our patients.
| Competing Interests|| |
All authors declare no competing interests.
| References|| |
|1.||Serefoglu EC, Saitz TR. New insights on premature ejaculation: a review of definition, classification, prevalence and treatment. Asian J Androl 2012; 14: 822−9. |
|2.||Waldinger MD, Berendsen HH, Blok BF, Olivier B, Holstege G. Premature ejaculation and serotonergic antidepressants-induced delayed ejaculation: the involvement of the serotonergic system. Behav Brain Res 1998; 92: 111−8. |
|3.||Janssen PK, Bakker SC, Réthelyi J, Zwinderman AH, Touw DJ, et al. Serotonin transporter promoter region (5-HTTLPR) polymorphism is associated with the intravaginal ejaculation latency time in Dutch men with lifelong premature ejaculation. J Sex Med 2009; 6: 276−84. |
|4.||Janssen PK, van Schaik R, Zwinderman AH, Olivier B, Waldinger MD. The 5-HT1A receptor gene C (1019) G polymorphism influences the intravaginal ejaculation latency time in Dutch Caucasian men with lifelong premature ejaculation. Pharmacol Biochem Behav 2014 Jan 15. [Epub ahead of print]. |
|5.||Luo S, Lu Y, Wang F, Xie Z, Huang X, et al. Association between polymorphisms in the serotonin 2C receptor gene and premature ejaculation in Han Chinese subjects. Urol Int 2010; 85: 204-8. |
|6.||Janssen PKC, van Schaik R, Olivier B, Waldinger MD. The 5-HT2C receptor gene Cys23Ser polymorphism influences the intravaginal ejaculation latency time in Dutch Caucasian men with lifelong premature ejaculation. Asian J Androl. 2014; doi: 10.4103/1008-682X.126371. |