Meyer-Bahlburg Heino F L, Dolezal Curtis, Baker Susan W, New Maria I
New York State Psychiatric Institute & Department of Psychiatry, Columbia University, 1051 Riverside Drive, New York, NY 10032, USA.
Arch Sex Behav. 2008 Feb;37(1):85-99. doi: 10.1007/s10508-007-9265-1.
46,XX individuals with classical congenital adrenal hyperplasia (CAH) due to deficiency of the enzyme, 21-hydroxylase, show variable degrees of masculinization of body and behavior due to excess adrenal androgen production. Increased bisexuality and homosexuality have also been reported. This article provides a review of existing reports of the latter and presents a new study aimed at replicating the previous findings with detailed assessments of sexual orientation on relatively large samples, and at extending the investigation to the mildest form, non-classical (NC) CAH. Also, this is the first study to relate sexual orientation to the specific molecular genotypes of CAH. In the present study, 40 salt-wasters (SW), 21 SV (simple-virilizing), 82 NC, and 24 non-CAH control women (sisters and female cousins of CAH women) were blindly administered the Sexual Behavior Assessment Schedule (SEBAS-A, 1983 ed.; H. F. L. Meyer-Bahlburg & A. A. Ehrhardt, Privately printed). Most women were heterosexual, but the rates of bisexual and homosexual orientation were increased above controls not only in women with classical CAH, but also in NC women, and correlated with the degree of prenatal androgenization. Classifying women by molecular genotypes did not further increase the correlation. Diverse aspects of sexual orientation were highly intercorrelated, and principal components analysis yielded one general factor. Bisexual/homosexual orientation was (modestly) correlated with global measures of masculinization of non-sexual behavior and predicted independently by the degree of both prenatal androgenization and masculinization of childhood behavior. We conclude that the findings support a sexual-differentiation perspective involving prenatal androgens on the development of sexual orientation.
由于21-羟化酶缺乏导致经典型先天性肾上腺皮质增生症(CAH)的46,XX个体,因肾上腺雄激素分泌过多而表现出不同程度的身体和行为男性化。也有报道称双性恋和同性恋发生率增加。本文回顾了关于后者的现有报告,并开展了一项新研究,旨在通过对相对大样本的性取向进行详细评估来重现先前的研究结果,并将调查扩展至最轻微的形式,即非经典型(NC)CAH。此外,这是第一项将性取向与CAH的特定分子基因型相关联的研究。在本研究中,对40名失盐型(SW)、21名单纯男性化型(SV)、82名NC型以及24名非CAH对照女性(CAH女性的姐妹和女性表亲)采用盲法进行了性行为评估量表(SEBAS-A,1983年版;H.F.L.迈耶 - 巴尔堡和A.A.埃尔哈特,内部印刷)评估。大多数女性为异性恋,但不仅经典型CAH女性,NC型女性中双性恋和同性恋取向的比例也高于对照组,且与产前雄激素化程度相关。按分子基因型对女性进行分类并未进一步增强这种相关性。性取向的不同方面高度相互关联,主成分分析得出一个一般因素。双性恋/同性恋取向与非性行为男性化的总体测量值(适度)相关,并由产前雄激素化程度和儿童期行为男性化程度独立预测。我们得出结论,这些发现支持了一种涉及产前雄激素对性取向发展影响的性分化观点。