{"title":"大学生性激素相关基因重复数多态性与性别表型变异的关系","authors":"Mizuho Igarashi, Yuko Katoh-Fukui, Atsushi Hattori, Kyongsun Pak, Shoko Sasaki, Maki Fukami","doi":"10.1093/sexmed/qfaf060","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Although common repeat number polymorphisms in 3 hormone-related genes (<i>AR</i>, <i>CYP19A1</i>, and <i>ESR2</i>) have been implicated in the variations in several sexually dimorphic phenotypes, their contributions to the variations in gender identity (GI) and sexual orientation (SO) remain to be clarified.</p><p><strong>Aim: </strong>To clarify the possible association between the repeat number polymorphisms and gender phenotype variations in the general population.</p><p><strong>Methods: </strong>We used paper-based questionnaires to select 80 individuals with atypical gender phenotypes (the case group) and 114 control individuals (the control group) from 736 university students. The case group was further divided into two subgroups: one consisted of individuals with low GI scores (the atypical GI subgroup), and the other consisted of individuals with non-heterosexual orientation (the atypical SO subgroup). Repeat numbers of the longer and shorter alleles in each participant (Alleles 1 and 2) were examined through microsatellite analysis. Repeat numbers of <i>AR</i> in females were adjusted for the X chromosome inactivation status.</p><p><strong>Outcomes: </strong>We examined the statistical differences in the repeat numbers between the case and control groups, and between each subgroup and the control group.</p><p><strong>Results: </strong>The overall differences between the case and control groups and between each subgroup and the control group were small. However, the repeat numbers of <i>AR</i> in males of the case group were larger than those of the control group (<i>P</i> = 0.049), and the repeat numbers of <i>ESR2</i> Allele 1 were larger in males of the atypical GI subgroup than in those of the control group (<i>P</i> = 0.046). In addition, females in the atypical SO subgroup had smaller repeat numbers of <i>CYP19A1</i> Allele 2 than control females (<i>P</i> = 0.011).</p><p><strong>Clinical implications: </strong>These results indicate the complex genetic basis of gender phenotype variations.</p><p><strong>Strengths & limitations: </strong>This is the first study that addresses the possible association between common polymorphisms in hormone-related genes and gender phenotypes in the general population. Given the small number of our subjects and the modest differences in the repeat numbers between the case and control groups, our results await further validation.</p><p><strong>Conclusion: </strong>The results indicate that the contribution of repeat number polymorphisms of the 3 genes to gender phenotype variations in the general population is small, although the repeat numbers of <i>AR</i> and <i>ESR2</i> are potentially associated with atypical gender phenotypes in males.</p>","PeriodicalId":21782,"journal":{"name":"Sexual Medicine","volume":"13 4","pages":"qfaf060"},"PeriodicalIF":2.0000,"publicationDate":"2025-08-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12358044/pdf/","citationCount":"0","resultStr":"{\"title\":\"Association between repeat number polymorphisms of sex hormone-related genes and gender phenotype variations in university students.\",\"authors\":\"Mizuho Igarashi, Yuko Katoh-Fukui, Atsushi Hattori, Kyongsun Pak, Shoko Sasaki, Maki Fukami\",\"doi\":\"10.1093/sexmed/qfaf060\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Although common repeat number polymorphisms in 3 hormone-related genes (<i>AR</i>, <i>CYP19A1</i>, and <i>ESR2</i>) have been implicated in the variations in several sexually dimorphic phenotypes, their contributions to the variations in gender identity (GI) and sexual orientation (SO) remain to be clarified.</p><p><strong>Aim: </strong>To clarify the possible association between the repeat number polymorphisms and gender phenotype variations in the general population.</p><p><strong>Methods: </strong>We used paper-based questionnaires to select 80 individuals with atypical gender phenotypes (the case group) and 114 control individuals (the control group) from 736 university students. The case group was further divided into two subgroups: one consisted of individuals with low GI scores (the atypical GI subgroup), and the other consisted of individuals with non-heterosexual orientation (the atypical SO subgroup). Repeat numbers of the longer and shorter alleles in each participant (Alleles 1 and 2) were examined through microsatellite analysis. Repeat numbers of <i>AR</i> in females were adjusted for the X chromosome inactivation status.</p><p><strong>Outcomes: </strong>We examined the statistical differences in the repeat numbers between the case and control groups, and between each subgroup and the control group.</p><p><strong>Results: </strong>The overall differences between the case and control groups and between each subgroup and the control group were small. However, the repeat numbers of <i>AR</i> in males of the case group were larger than those of the control group (<i>P</i> = 0.049), and the repeat numbers of <i>ESR2</i> Allele 1 were larger in males of the atypical GI subgroup than in those of the control group (<i>P</i> = 0.046). In addition, females in the atypical SO subgroup had smaller repeat numbers of <i>CYP19A1</i> Allele 2 than control females (<i>P</i> = 0.011).</p><p><strong>Clinical implications: </strong>These results indicate the complex genetic basis of gender phenotype variations.</p><p><strong>Strengths & limitations: </strong>This is the first study that addresses the possible association between common polymorphisms in hormone-related genes and gender phenotypes in the general population. Given the small number of our subjects and the modest differences in the repeat numbers between the case and control groups, our results await further validation.</p><p><strong>Conclusion: </strong>The results indicate that the contribution of repeat number polymorphisms of the 3 genes to gender phenotype variations in the general population is small, although the repeat numbers of <i>AR</i> and <i>ESR2</i> are potentially associated with atypical gender phenotypes in males.</p>\",\"PeriodicalId\":21782,\"journal\":{\"name\":\"Sexual Medicine\",\"volume\":\"13 4\",\"pages\":\"qfaf060\"},\"PeriodicalIF\":2.0000,\"publicationDate\":\"2025-08-17\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12358044/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Sexual Medicine\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1093/sexmed/qfaf060\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/8/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q1\",\"JCRName\":\"MEDICINE, GENERAL & INTERNAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Sexual Medicine","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1093/sexmed/qfaf060","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/8/1 0:00:00","PubModel":"eCollection","JCR":"Q1","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}
Association between repeat number polymorphisms of sex hormone-related genes and gender phenotype variations in university students.
Background: Although common repeat number polymorphisms in 3 hormone-related genes (AR, CYP19A1, and ESR2) have been implicated in the variations in several sexually dimorphic phenotypes, their contributions to the variations in gender identity (GI) and sexual orientation (SO) remain to be clarified.
Aim: To clarify the possible association between the repeat number polymorphisms and gender phenotype variations in the general population.
Methods: We used paper-based questionnaires to select 80 individuals with atypical gender phenotypes (the case group) and 114 control individuals (the control group) from 736 university students. The case group was further divided into two subgroups: one consisted of individuals with low GI scores (the atypical GI subgroup), and the other consisted of individuals with non-heterosexual orientation (the atypical SO subgroup). Repeat numbers of the longer and shorter alleles in each participant (Alleles 1 and 2) were examined through microsatellite analysis. Repeat numbers of AR in females were adjusted for the X chromosome inactivation status.
Outcomes: We examined the statistical differences in the repeat numbers between the case and control groups, and between each subgroup and the control group.
Results: The overall differences between the case and control groups and between each subgroup and the control group were small. However, the repeat numbers of AR in males of the case group were larger than those of the control group (P = 0.049), and the repeat numbers of ESR2 Allele 1 were larger in males of the atypical GI subgroup than in those of the control group (P = 0.046). In addition, females in the atypical SO subgroup had smaller repeat numbers of CYP19A1 Allele 2 than control females (P = 0.011).
Clinical implications: These results indicate the complex genetic basis of gender phenotype variations.
Strengths & limitations: This is the first study that addresses the possible association between common polymorphisms in hormone-related genes and gender phenotypes in the general population. Given the small number of our subjects and the modest differences in the repeat numbers between the case and control groups, our results await further validation.
Conclusion: The results indicate that the contribution of repeat number polymorphisms of the 3 genes to gender phenotype variations in the general population is small, although the repeat numbers of AR and ESR2 are potentially associated with atypical gender phenotypes in males.
期刊介绍:
Sexual Medicine is an official publication of the International Society for Sexual Medicine, and serves the field as the peer-reviewed, open access journal for rapid dissemination of multidisciplinary clinical and basic research in all areas of global sexual medicine, and particularly acts as a venue for topics of regional or sub-specialty interest. The journal is focused on issues in clinical medicine and epidemiology but also publishes basic science papers with particular relevance to specific populations. Sexual Medicine offers clinicians and researchers a rapid route to publication and the opportunity to publish in a broadly distributed and highly visible global forum. The journal publishes high quality articles from all over the world and actively seeks submissions from countries with expanding sexual medicine communities. Sexual Medicine relies on the same expert panel of editors and reviewers as The Journal of Sexual Medicine and Sexual Medicine Reviews.