Meyer-Bahlburg H F
Clin Endocrinol Metab. 1982 Nov;11(3):681-701. doi: 10.1016/s0300-595x(82)80007-8.
During fetal development of subprimate mammals, sexual differentiation of the genitals and of specific sex-dimorphic brain systems depends on androgens; corresponding sex differences are displayed in prepubertal behaviours as well as in behaviours that depend on activation by pubertal hormones. In human beings, fetal hormones play the same role in genital differentiation. Hormone-dependent structural brain changes are also very likely but have not yet been demonstrated. The corresponding effects of fetal hormones on childhood behaviour have been found both in subhuman primates and in man, while the evidence concerning later behaviour, including sexual orientation, is not yet clear. The development of gender identity in humans is a cognitive process that has no counterpart in animal behaviour and is unlikely to be based on a specific hormone-sensitive brain system. It appears that the hormone-dependent variations of sex-dimorphic behaviour in childhood can be accommodated within either gender identity, provided that the child's physical appearance is gender adequate and the parental (or other caregivers') rearing style does not interfere with typical gender role development. In intersex individuals, changes in gender identity seem to occur primarily when genital and/or general physical appearance are in conflict with the assigned gender and/or when rearing has been ambiguous. The available descriptions of such changes do not seem compatible with a primarily neuroendocrine explanation. Thus, decisions on sex assignment and reassignment of intersex patients need to be based on expected social and sexual functioning, and the clinical management of such patients must minimize the risk of ambiguous rearing and of the development of a gender-incongruent physical appearance. The development of a sexual orientation in humans as hetero- or homosexual does not seem to depend on pubertal hormones. The evidence for a role of fetal hormones is suggestive, but the issue is not yet settled. Attempts to implicate the H-Y antigen in the aetiology of transsexuality seem to have failed; psychoendocrine research here parallels that on sexual orientation. Some recent developments in the management of transsexual patients are discussed.
在灵长类以下哺乳动物的胎儿发育过程中,生殖器以及特定性别二态性脑系统的性分化依赖于雄激素;相应的性别差异在青春期前行为以及依赖青春期激素激活的行为中也有表现。在人类中,胎儿激素在生殖器分化中发挥相同作用。激素依赖性脑结构变化也极有可能存在,但尚未得到证实。胎儿激素对儿童行为的相应影响在非人类灵长类动物和人类中均已发现,而关于包括性取向在内的后期行为的证据尚不明确。人类性别认同的发展是一个认知过程,在动物行为中没有对应物,也不太可能基于特定的激素敏感脑系统。似乎童年时期依赖激素的性别二态性行为变化可以在任何一种性别认同中得到适应,只要孩子的外貌符合性别特征,且父母(或其他照顾者)的养育方式不干扰典型的性别角色发展。在两性畸形个体中,性别认同的变化似乎主要发生在生殖器和/或总体外貌与指定性别冲突时,以及/或者养育方式不明确时。对此类变化的现有描述似乎与主要的神经内分泌解释不相符。因此,两性畸形患者的性别指定和重新指定决策需要基于预期的社会和性功能,对此类患者的临床管理必须将模糊养育和性别不一致外貌发展的风险降至最低。人类作为异性恋或同性恋的性取向发展似乎不依赖于青春期激素。胎儿激素起作用的证据具有启发性,但这个问题尚未解决。将H-Y抗原与易性癖病因联系起来的尝试似乎失败了;这里的心理内分泌研究与性取向研究类似。本文讨论了易性癖患者管理方面的一些最新进展。