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2D:4D Suggests a Role of Prenatal Testosterone in Gender Dysphoria
Gender dysphoria (GD) reflects distress caused by incongruence between one’s experienced gender identity and one’s natal (assigned) gender. Previous studies suggest that high levels of prenatal testosterone (T) in natal females and low levels in natal males might contribute to GD. Here, we investiga...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer US
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7031197/ https://www.ncbi.nlm.nih.gov/pubmed/31975034 http://dx.doi.org/10.1007/s10508-020-01630-0 |
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author | Sadr, Mostafa Khorashad, Behzad S. Talaei, Ali Fazeli, Nasrin Hönekopp, Johannes |
author_facet | Sadr, Mostafa Khorashad, Behzad S. Talaei, Ali Fazeli, Nasrin Hönekopp, Johannes |
author_sort | Sadr, Mostafa |
collection | PubMed |
description | Gender dysphoria (GD) reflects distress caused by incongruence between one’s experienced gender identity and one’s natal (assigned) gender. Previous studies suggest that high levels of prenatal testosterone (T) in natal females and low levels in natal males might contribute to GD. Here, we investigated if the 2D:4D digit ratio, a biomarker of prenatal T effects, is related to GD. We first report results from a large Iranian sample, comparing 2D:4D in 104 transwomen and 89 transmen against controls of the same natal sex. We found significantly lower (less masculine) 2D:4D in transwomen compared to control men. We then conducted random-effects meta-analyses of relevant studies including our own (k = 6, N = 925 for transwomen and k = 6, N = 757 for transmen). In line with the hypothesized prenatal T effects, transwomen showed significantly feminized 2D:4D (d ≈ 0.24). Conversely, transmen showed masculinized 2D:4D (d ≈ − 0.28); however, large unaccounted heterogeneity across studies emerged, which makes this effect less meaningful. These findings support the idea that high levels of prenatal T in natal females and low levels in natal males play a part in the etiology of GD. As we discuss, this adds to the evidence demonstrating the convergent validity of 2D:4D as a marker of prenatal T effects. |
format | Online Article Text |
id | pubmed-7031197 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-70311972020-03-03 2D:4D Suggests a Role of Prenatal Testosterone in Gender Dysphoria Sadr, Mostafa Khorashad, Behzad S. Talaei, Ali Fazeli, Nasrin Hönekopp, Johannes Arch Sex Behav Original Paper Gender dysphoria (GD) reflects distress caused by incongruence between one’s experienced gender identity and one’s natal (assigned) gender. Previous studies suggest that high levels of prenatal testosterone (T) in natal females and low levels in natal males might contribute to GD. Here, we investigated if the 2D:4D digit ratio, a biomarker of prenatal T effects, is related to GD. We first report results from a large Iranian sample, comparing 2D:4D in 104 transwomen and 89 transmen against controls of the same natal sex. We found significantly lower (less masculine) 2D:4D in transwomen compared to control men. We then conducted random-effects meta-analyses of relevant studies including our own (k = 6, N = 925 for transwomen and k = 6, N = 757 for transmen). In line with the hypothesized prenatal T effects, transwomen showed significantly feminized 2D:4D (d ≈ 0.24). Conversely, transmen showed masculinized 2D:4D (d ≈ − 0.28); however, large unaccounted heterogeneity across studies emerged, which makes this effect less meaningful. These findings support the idea that high levels of prenatal T in natal females and low levels in natal males play a part in the etiology of GD. As we discuss, this adds to the evidence demonstrating the convergent validity of 2D:4D as a marker of prenatal T effects. Springer US 2020-01-23 2020 /pmc/articles/PMC7031197/ /pubmed/31975034 http://dx.doi.org/10.1007/s10508-020-01630-0 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Original Paper Sadr, Mostafa Khorashad, Behzad S. Talaei, Ali Fazeli, Nasrin Hönekopp, Johannes 2D:4D Suggests a Role of Prenatal Testosterone in Gender Dysphoria |
title | 2D:4D Suggests a Role of Prenatal Testosterone in Gender Dysphoria |
title_full | 2D:4D Suggests a Role of Prenatal Testosterone in Gender Dysphoria |
title_fullStr | 2D:4D Suggests a Role of Prenatal Testosterone in Gender Dysphoria |
title_full_unstemmed | 2D:4D Suggests a Role of Prenatal Testosterone in Gender Dysphoria |
title_short | 2D:4D Suggests a Role of Prenatal Testosterone in Gender Dysphoria |
title_sort | 2d:4d suggests a role of prenatal testosterone in gender dysphoria |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7031197/ https://www.ncbi.nlm.nih.gov/pubmed/31975034 http://dx.doi.org/10.1007/s10508-020-01630-0 |
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