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Sexual Orientation in Individuals With Congenital Adrenal Hyperplasia: A Systematic Review

Congenital adrenal hyperplasia (CAH) is a genetic condition of the steroidogenic enzymes in the adrenal cortex normally leading to variable degrees of cortisol and aldosterone deficiency as well as androgen excess. Exposure to androgens prenatally might lead to ambiguous genitalia. The fetal brain d...

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Autores principales: Daae, Elisabeth, Feragen, Kristin Billaud, Waehre, Anne, Nermoen, Ingrid, Falhammar, Henrik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7082355/
https://www.ncbi.nlm.nih.gov/pubmed/32231525
http://dx.doi.org/10.3389/fnbeh.2020.00038
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author Daae, Elisabeth
Feragen, Kristin Billaud
Waehre, Anne
Nermoen, Ingrid
Falhammar, Henrik
author_facet Daae, Elisabeth
Feragen, Kristin Billaud
Waehre, Anne
Nermoen, Ingrid
Falhammar, Henrik
author_sort Daae, Elisabeth
collection PubMed
description Congenital adrenal hyperplasia (CAH) is a genetic condition of the steroidogenic enzymes in the adrenal cortex normally leading to variable degrees of cortisol and aldosterone deficiency as well as androgen excess. Exposure to androgens prenatally might lead to ambiguous genitalia. The fetal brain develops in traditional male direction through a direct action of androgens on the developing nerve cells, or in the traditional female direction in the absence of androgens. This may indicate that sexual development, including sexual orientation, are programmed into our brain structures prenatally. The objective of this study was to perform a systematic review of the literature, investigating sexual orientation in individuals with CAH. The study also aimed at identifying which measures are used to define sexual orientation across studies. The review is based on articles identified through a comprehensive search of the OVIDMedline, PsycINFO, CINAHL, and Web of Science databases published up to May 2019. All peer-reviewed articles investigating sexual orientation in people with CAH were included. Quantitative, qualitative, and mixed methods were considered, as well as self-, parent-, and third-party reports, and no age or language restrictions were enforced on publications. The present review included 30 studies investigating sexual orientation in patients with CAH assigned female at birth (46, XX) (n = 927) or assigned male at birth (46, XY and 46, XX) (n = 274). Results indicate that assigned females at birth (46, XX) with CAH had a greater likelihood to not have an exclusively heterosexual orientation than females from the general population, whereas no assigned males at birth (46, XY or 46, XX) with CAH identified themselves as non-heterosexual. There was a wide diversity in measures used and a preference for unvalidated and self-constructed interviews. Hence, the results need to be interpreted with caution. Methodological weaknesses might have led to non-heterosexual orientation being overestimated or underestimated. The methodological challenges identified by this review should be further investigated in future studies.
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spelling pubmed-70823552020-03-30 Sexual Orientation in Individuals With Congenital Adrenal Hyperplasia: A Systematic Review Daae, Elisabeth Feragen, Kristin Billaud Waehre, Anne Nermoen, Ingrid Falhammar, Henrik Front Behav Neurosci Behavioral Neuroscience Congenital adrenal hyperplasia (CAH) is a genetic condition of the steroidogenic enzymes in the adrenal cortex normally leading to variable degrees of cortisol and aldosterone deficiency as well as androgen excess. Exposure to androgens prenatally might lead to ambiguous genitalia. The fetal brain develops in traditional male direction through a direct action of androgens on the developing nerve cells, or in the traditional female direction in the absence of androgens. This may indicate that sexual development, including sexual orientation, are programmed into our brain structures prenatally. The objective of this study was to perform a systematic review of the literature, investigating sexual orientation in individuals with CAH. The study also aimed at identifying which measures are used to define sexual orientation across studies. The review is based on articles identified through a comprehensive search of the OVIDMedline, PsycINFO, CINAHL, and Web of Science databases published up to May 2019. All peer-reviewed articles investigating sexual orientation in people with CAH were included. Quantitative, qualitative, and mixed methods were considered, as well as self-, parent-, and third-party reports, and no age or language restrictions were enforced on publications. The present review included 30 studies investigating sexual orientation in patients with CAH assigned female at birth (46, XX) (n = 927) or assigned male at birth (46, XY and 46, XX) (n = 274). Results indicate that assigned females at birth (46, XX) with CAH had a greater likelihood to not have an exclusively heterosexual orientation than females from the general population, whereas no assigned males at birth (46, XY or 46, XX) with CAH identified themselves as non-heterosexual. There was a wide diversity in measures used and a preference for unvalidated and self-constructed interviews. Hence, the results need to be interpreted with caution. Methodological weaknesses might have led to non-heterosexual orientation being overestimated or underestimated. The methodological challenges identified by this review should be further investigated in future studies. Frontiers Media S.A. 2020-03-13 /pmc/articles/PMC7082355/ /pubmed/32231525 http://dx.doi.org/10.3389/fnbeh.2020.00038 Text en Copyright © 2020 Daae, Feragen, Waehre, Nermoen and Falhammar. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Behavioral Neuroscience
Daae, Elisabeth
Feragen, Kristin Billaud
Waehre, Anne
Nermoen, Ingrid
Falhammar, Henrik
Sexual Orientation in Individuals With Congenital Adrenal Hyperplasia: A Systematic Review
title Sexual Orientation in Individuals With Congenital Adrenal Hyperplasia: A Systematic Review
title_full Sexual Orientation in Individuals With Congenital Adrenal Hyperplasia: A Systematic Review
title_fullStr Sexual Orientation in Individuals With Congenital Adrenal Hyperplasia: A Systematic Review
title_full_unstemmed Sexual Orientation in Individuals With Congenital Adrenal Hyperplasia: A Systematic Review
title_short Sexual Orientation in Individuals With Congenital Adrenal Hyperplasia: A Systematic Review
title_sort sexual orientation in individuals with congenital adrenal hyperplasia: a systematic review
topic Behavioral Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7082355/
https://www.ncbi.nlm.nih.gov/pubmed/32231525
http://dx.doi.org/10.3389/fnbeh.2020.00038
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