Gene Variants in Premature Ejaculation: Systematic Review and Future Directions
A growing number of genetic association studies have been performed to investigate the association between the genetic susceptibility alleles and the risk of premature ejaculation (PE); however, the results remain inconclusive. This systematic review aimed: (i) to determine whether an association ex...
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description | A growing number of genetic association studies have been performed to investigate the association between the genetic susceptibility alleles and the risk of premature ejaculation (PE); however, the results remain inconclusive.
This systematic review aimed: (i) to determine whether an association exists between gene(s) or allelic variant(s) and PE; (ii) to assess whether the associations are consistent across studies in magnitude and direction, and (iii) to identify any limitation, gap, or shortcoming in the included studies.
The literature search was conducted in PubMed, MEDLINE, Scopus, Cochrane Library, EMBASE, Academic Search Complete, Google Scholar, and CINAHL databases.
Different gene variants associated with PE were assessed. 25 genetic association studies met the inclusion criteria that investigated 11 genes, 2,624 men with PE compared with 9,346 men as controls, twins, and siblings. 19 studies demonstrated a significant association with PE, whereas 4 studies denied such a relationship. SLC6A4 gene polymorphism was investigated in 11 studies (7 studies demonstrated a significant relationship with PE, and 4 studies denied such a relationship). Dopamine transporter gene (DAT1) polymorphism was investigated in 4 studies exhibiting a significant relationship. Androgen receptor gene polymorphisms were investigated in 2 studies, 1 with a significant relationship and the other with a non-significant relationship. Oxytocin gene polymorphisms and tryptophan hydroxylase 2 gene polymorphisms were investigated in 2 studies with a significant relationship.
While this review has highlighted several genes that may be potentially associated with PE such as SLC6A4, limitations such as variance in study methods, lack of robust findings, small sample sizes, lack of reproducibility, quality of reporting, and quality of assessment remain a major concern. Further efforts such as standardizing reporting, exploring complementary designs, and the use of genome-wide association studies technology are warranted to test the reproducibility of these early findings.
Mostafa T, Abdel-Hamid IA, Taymour M, et al. Gene Variants in Premature Ejaculation: Systematic Review and Future Directions. Sex Med Rev 2020;8:586–602. |
doi_str_mv | 10.1016/j.sxmr.2020.07.002 |
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This systematic review aimed: (i) to determine whether an association exists between gene(s) or allelic variant(s) and PE; (ii) to assess whether the associations are consistent across studies in magnitude and direction, and (iii) to identify any limitation, gap, or shortcoming in the included studies.
The literature search was conducted in PubMed, MEDLINE, Scopus, Cochrane Library, EMBASE, Academic Search Complete, Google Scholar, and CINAHL databases.
Different gene variants associated with PE were assessed. 25 genetic association studies met the inclusion criteria that investigated 11 genes, 2,624 men with PE compared with 9,346 men as controls, twins, and siblings. 19 studies demonstrated a significant association with PE, whereas 4 studies denied such a relationship. SLC6A4 gene polymorphism was investigated in 11 studies (7 studies demonstrated a significant relationship with PE, and 4 studies denied such a relationship). Dopamine transporter gene (DAT1) polymorphism was investigated in 4 studies exhibiting a significant relationship. Androgen receptor gene polymorphisms were investigated in 2 studies, 1 with a significant relationship and the other with a non-significant relationship. Oxytocin gene polymorphisms and tryptophan hydroxylase 2 gene polymorphisms were investigated in 2 studies with a significant relationship.
While this review has highlighted several genes that may be potentially associated with PE such as SLC6A4, limitations such as variance in study methods, lack of robust findings, small sample sizes, lack of reproducibility, quality of reporting, and quality of assessment remain a major concern. Further efforts such as standardizing reporting, exploring complementary designs, and the use of genome-wide association studies technology are warranted to test the reproducibility of these early findings.
Mostafa T, Abdel-Hamid IA, Taymour M, et al. Gene Variants in Premature Ejaculation: Systematic Review and Future Directions. Sex Med Rev 2020;8:586–602.</description><identifier>ISSN: 2050-0521</identifier><identifier>EISSN: 2050-0521</identifier><identifier>DOI: 10.1016/j.sxmr.2020.07.002</identifier><identifier>PMID: 32800770</identifier><language>eng</language><publisher>Netherlands: Elsevier Inc</publisher><subject>Ejaculation ; Genes ; Polymorphisms ; Premature Ejaculation</subject><ispartof>Sexual medicine reviews, 2020-10, Vol.8 (4), p.586-602</ispartof><rights>2020 International Society for Sexual Medicine</rights><rights>Copyright © 2020 International Society for Sexual Medicine. Published by Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c356t-ecead023b8b37e9fdf8f8ea441381ce9f732212df525f527b87a321d65a43d893</citedby><cites>FETCH-LOGICAL-c356t-ecead023b8b37e9fdf8f8ea441381ce9f732212df525f527b87a321d65a43d893</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32800770$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mostafa, Taymour</creatorcontrib><creatorcontrib>Abdel-Hamid, Ibrahim A.</creatorcontrib><creatorcontrib>Taymour, Mai</creatorcontrib><creatorcontrib>Ali, Omar I.</creatorcontrib><title>Gene Variants in Premature Ejaculation: Systematic Review and Future Directions</title><title>Sexual medicine reviews</title><addtitle>Sex Med Rev</addtitle><description>A growing number of genetic association studies have been performed to investigate the association between the genetic susceptibility alleles and the risk of premature ejaculation (PE); however, the results remain inconclusive.
This systematic review aimed: (i) to determine whether an association exists between gene(s) or allelic variant(s) and PE; (ii) to assess whether the associations are consistent across studies in magnitude and direction, and (iii) to identify any limitation, gap, or shortcoming in the included studies.
The literature search was conducted in PubMed, MEDLINE, Scopus, Cochrane Library, EMBASE, Academic Search Complete, Google Scholar, and CINAHL databases.
Different gene variants associated with PE were assessed. 25 genetic association studies met the inclusion criteria that investigated 11 genes, 2,624 men with PE compared with 9,346 men as controls, twins, and siblings. 19 studies demonstrated a significant association with PE, whereas 4 studies denied such a relationship. SLC6A4 gene polymorphism was investigated in 11 studies (7 studies demonstrated a significant relationship with PE, and 4 studies denied such a relationship). Dopamine transporter gene (DAT1) polymorphism was investigated in 4 studies exhibiting a significant relationship. Androgen receptor gene polymorphisms were investigated in 2 studies, 1 with a significant relationship and the other with a non-significant relationship. Oxytocin gene polymorphisms and tryptophan hydroxylase 2 gene polymorphisms were investigated in 2 studies with a significant relationship.
While this review has highlighted several genes that may be potentially associated with PE such as SLC6A4, limitations such as variance in study methods, lack of robust findings, small sample sizes, lack of reproducibility, quality of reporting, and quality of assessment remain a major concern. Further efforts such as standardizing reporting, exploring complementary designs, and the use of genome-wide association studies technology are warranted to test the reproducibility of these early findings.
Mostafa T, Abdel-Hamid IA, Taymour M, et al. Gene Variants in Premature Ejaculation: Systematic Review and Future Directions. Sex Med Rev 2020;8:586–602.</description><subject>Ejaculation</subject><subject>Genes</subject><subject>Polymorphisms</subject><subject>Premature Ejaculation</subject><issn>2050-0521</issn><issn>2050-0521</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp9kE1LxDAQhoMoKuv-AQ_So5fWSdJuWvEiun7Awopf15BNppClH2vSqvvvTXdVPBkYMkyeeSEPIccUEgp0crZM_GftEgYMEhAJANshhwwyiCFjdPdPf0DG3i8hnKLgPC32yQFnOYAQcEjmt9hg9KqcVU3nI9tEDw5r1fUOo-lS6b5SnW2b8-hp7bvhweroEd8tfkSqMdFNvyGvrUM9cP6I7JWq8jj-vkfk5Wb6fHUXz-a391eXs1jzbNLFqFEZYHyRL7jAojRlXuao0pTynOowEJwxykyZsSyUWORCcUbNJFMpN3nBR-R0m7ty7VuPvpO19RqrSjXY9l6ylKciy4FPAsq2qHat9w5LuXK2Vm4tKcjBpVzKwaUcXEoQMrgMSyff-f2iRvO78mMuABdbAMMvgw8nvbbYaDQbF9K09r_8LxwYhSo</recordid><startdate>202010</startdate><enddate>202010</enddate><creator>Mostafa, Taymour</creator><creator>Abdel-Hamid, Ibrahim A.</creator><creator>Taymour, Mai</creator><creator>Ali, Omar I.</creator><general>Elsevier Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>202010</creationdate><title>Gene Variants in Premature Ejaculation: Systematic Review and Future Directions</title><author>Mostafa, Taymour ; Abdel-Hamid, Ibrahim A. ; Taymour, Mai ; Ali, Omar I.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c356t-ecead023b8b37e9fdf8f8ea441381ce9f732212df525f527b87a321d65a43d893</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Ejaculation</topic><topic>Genes</topic><topic>Polymorphisms</topic><topic>Premature Ejaculation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mostafa, Taymour</creatorcontrib><creatorcontrib>Abdel-Hamid, Ibrahim A.</creatorcontrib><creatorcontrib>Taymour, Mai</creatorcontrib><creatorcontrib>Ali, Omar I.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Sexual medicine reviews</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mostafa, Taymour</au><au>Abdel-Hamid, Ibrahim A.</au><au>Taymour, Mai</au><au>Ali, Omar I.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Gene Variants in Premature Ejaculation: Systematic Review and Future Directions</atitle><jtitle>Sexual medicine reviews</jtitle><addtitle>Sex Med Rev</addtitle><date>2020-10</date><risdate>2020</risdate><volume>8</volume><issue>4</issue><spage>586</spage><epage>602</epage><pages>586-602</pages><issn>2050-0521</issn><eissn>2050-0521</eissn><abstract>A growing number of genetic association studies have been performed to investigate the association between the genetic susceptibility alleles and the risk of premature ejaculation (PE); however, the results remain inconclusive.
This systematic review aimed: (i) to determine whether an association exists between gene(s) or allelic variant(s) and PE; (ii) to assess whether the associations are consistent across studies in magnitude and direction, and (iii) to identify any limitation, gap, or shortcoming in the included studies.
The literature search was conducted in PubMed, MEDLINE, Scopus, Cochrane Library, EMBASE, Academic Search Complete, Google Scholar, and CINAHL databases.
Different gene variants associated with PE were assessed. 25 genetic association studies met the inclusion criteria that investigated 11 genes, 2,624 men with PE compared with 9,346 men as controls, twins, and siblings. 19 studies demonstrated a significant association with PE, whereas 4 studies denied such a relationship. SLC6A4 gene polymorphism was investigated in 11 studies (7 studies demonstrated a significant relationship with PE, and 4 studies denied such a relationship). Dopamine transporter gene (DAT1) polymorphism was investigated in 4 studies exhibiting a significant relationship. Androgen receptor gene polymorphisms were investigated in 2 studies, 1 with a significant relationship and the other with a non-significant relationship. Oxytocin gene polymorphisms and tryptophan hydroxylase 2 gene polymorphisms were investigated in 2 studies with a significant relationship.
While this review has highlighted several genes that may be potentially associated with PE such as SLC6A4, limitations such as variance in study methods, lack of robust findings, small sample sizes, lack of reproducibility, quality of reporting, and quality of assessment remain a major concern. Further efforts such as standardizing reporting, exploring complementary designs, and the use of genome-wide association studies technology are warranted to test the reproducibility of these early findings.
Mostafa T, Abdel-Hamid IA, Taymour M, et al. Gene Variants in Premature Ejaculation: Systematic Review and Future Directions. Sex Med Rev 2020;8:586–602.</abstract><cop>Netherlands</cop><pub>Elsevier Inc</pub><pmid>32800770</pmid><doi>10.1016/j.sxmr.2020.07.002</doi><tpages>17</tpages></addata></record> |
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subjects | Ejaculation Genes Polymorphisms Premature Ejaculation |
title | Gene Variants in Premature Ejaculation: Systematic Review and Future Directions |
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