Psychiatry and Behavioral Sciences Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.
Molecular Pathology Unit, Liverpool Clinical Laboratories, Liverpool, UK.
Arch Sex Behav. 2018 Nov;47(8):2287-2298. doi: 10.1007/s10508-018-1281-9. Epub 2018 Aug 20.
Disorders of sex development (DSD) are congenital conditions in which the typical genetic and hormonal profiles are affected and thereby the usual process of sexual differentiation. Most of these studies, however, have been conducted in Western countries. In the present study, preschool sex-typed activities of Iranian individuals with DSD and their age-matched non-affected male and female relatives were assessed using the Pre-School Activities Inventory (PSAI) modified for retrospective self-report. A total of 192 individuals participated in our study, including 33 46,XX individuals with congenital adrenal hyperplasia (CAH; M age = 10.36, SD = 5.52), 15 46,XY individuals with complete androgen insensitivity syndrome (CAIS; M age = 19.8, SD = 7.14), and 16 46,XY individuals with 5-alpha reductase deficiency type-2 (5α-RD-2; M age = 17.31, SD = 7.28), as well as one age-matched non-affected male and female relative for each patient. With regard to PSAI scores, male-identifying participants with 5α-RD-2 and male controls reported similar levels of male-typical childhood play. Female-identifying participants with 5α-RD-2 and CAH showed comparable scores: significantly less masculine and more feminine than male controls, but significantly more masculine and less feminine than females with CAIS and female controls. These findings support the role of androgens in the development of sex-typical childhood play behavior, with those being exposed to higher levels of fetal functional androgens expressing more masculine behavior at preschool ages.
性发育障碍(DSD)是一种先天性疾病,其中典型的遗传和激素特征受到影响,从而影响通常的性分化过程。然而,这些研究大多在西方国家进行。在本研究中,使用为回顾性自我报告而修改的学前活动量表(PSAI)评估了伊朗 DSD 个体及其年龄匹配的未受影响的男性和女性亲属的学前性别定型活动。共有 192 人参加了我们的研究,包括 33 名患有先天性肾上腺增生症(CAH;M 年龄=10.36,SD=5.52)的 46,XX 个体,15 名患有完全雄激素不敏感综合征(CAIS;M 年龄=19.8,SD=7.14)的 46,XY 个体和 16 名患有 5-α 还原酶缺陷 2 型(5α-RD-2;M 年龄=17.31,SD=7.28)的 46,XY 个体,以及每位患者的一位年龄匹配的未受影响的男性和女性亲属。就 PSAI 评分而言,5α-RD-2 的男性认同参与者和男性对照者报告了类似的男性典型儿童游戏水平。5α-RD-2 的女性认同参与者和 CAH 表现出相似的分数:明显比男性对照者少男性化和多女性化,但比 CAIS 女性和女性对照者明显更男性化和少女性化。这些发现支持雄激素在性别典型的儿童游戏行为发展中的作用,那些暴露于更高水平的胎儿功能性雄激素的个体在学前年龄表现出更男性化的行为。