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

      systematic-review

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          Abstract

          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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          Most cited references128

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          Organizing action of prenatally administered testosterone propionate on the tissues mediating mating behavior in the female guinea pig.

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            Gender differences in erotic plasticity: the female sex drive as socially flexible and responsive.

            Responding to controversies about the balance between nature and culture in determining human sexuality, the author proposes that the female sex drive is more malleable than the male in response to sociocultural and situational factors. A large assortment of evidence supports 3 predictions based on the hypothesis of female erotic plasticity: (a) Individual women will exhibit more variation across time than men in sexual behavior, (b) female sexuality will exhibit larger effects than male in response to most specific sociocultural variables, and (c) sexual attitude-behavior consistency will be lower for women than men. Several possible explanations for female erotic plasticity are reviewed, including adaptation to superior male political and physical power, the centrality of female change (from no to yes) as a prerequisite for intercourse, and the idea that women have a milder sex drive than men.
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              Reframing sexual differentiation of the brain.

              In the twentieth century, the dominant model of sexual differentiation stated that genetic sex (XX versus XY) causes differentiation of the gonads, which then secrete gonadal hormones that act directly on tissues to induce sex differences in function. This serial model of sexual differentiation was simple, unifying and seductive. Recent evidence, however, indicates that the linear model is incorrect and that sex differences arise in response to diverse sex-specific signals originating from inherent differences in the genome and involve cellular mechanisms that are specific to individual tissues or brain regions. Moreover, sex-specific effects of the environment reciprocally affect biology, sometimes profoundly, and must therefore be integrated into a realistic model of sexual differentiation. A more appropriate model is a parallel-interactive model that encompasses the roles of multiple molecular signals and pathways that differentiate males and females, including synergistic and compensatory interactions among pathways and an important role for the environment.
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                Author and article information

                Contributors
                Journal
                Front Behav Neurosci
                Front Behav Neurosci
                Front. Behav. Neurosci.
                Frontiers in Behavioral Neuroscience
                Frontiers Media S.A.
                1662-5153
                13 March 2020
                2020
                : 14
                : 38
                Affiliations
                [1] 1Oslo University , Oslo, Norway
                [2] 2Akershus University Hospital , Lillestrøm, Norway
                [3] 3Karolinska Institute, Karolinska University Hospital , Stockholm, Sweden
                Author notes

                Edited by: James Cherry, Boston University, United States

                Reviewed by: Berenice Bilharinho Mendonca, University of São Paulo, Brazil; David E. Sandberg, University of Michigan, United States

                *Correspondence: Elisabeth Daae elidaa@ 123456ous-hf.no

                This article was submitted to Behavioral Endocrinology, a section of the journal Frontiers in Behavioral Neuroscience

                Article
                10.3389/fnbeh.2020.00038
                7082355
                8f657e6f-b66b-4a35-8ac6-6d8e2af96d69
                Copyright © 2020 Daae, Feragen, Waehre, Nermoen and Falhammar.

                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.

                History
                : 20 November 2019
                : 21 February 2020
                Page count
                Figures: 1, Tables: 4, Equations: 0, References: 150, Pages: 22, Words: 17397
                Categories
                Behavioral Neuroscience
                Systematic Review

                Neurosciences
                21-hydroxylase deficiency,partnership,homosexuality,bisexuality,androgen effects
                Neurosciences
                21-hydroxylase deficiency, partnership, homosexuality, bisexuality, androgen effects

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