Department of Obstetrics and Gynecology, Wake Forest University, Winston-Salem, NC, USA.
Gynecol Endocrinol. 2012 Mar;28 Suppl 1:9-13. doi: 10.3109/09513590.2012.651929.
Modern methods of diagnosis have made the distinction between hypothalamic failure and ovarian failure routine. Failure of the orderly progression of hypothalamic gonadotrophin-releasing hormone (GnRH) → pituitary gonadotrophins → ovarian steroids and inhibin → hypothalamus/pituitary results in anovulation/amenorrhea. The hypothalamic connections that regulate the pattern and amplitude of GnRH pulses are plastic and respond to external/psychological conditions and internal/metabolic factors that may affect the hypothalamic substrate on which estrogen levels can act. We trace the neuroendocrine regulation of the ovarian cycle, concentrating on hypothalamic connections that underlie negative and positive feedback control of GnRH and the complementary role of the adenohypophysis. The main hormone regulating this "central axis" and the development of the endometrium is estradiol which is exported from the developing ovarian follicles and thereby closes the feedback loop with follicle development. Progesterone and inhibin are also involved. Neuroendocrine responses to internal and external factors can cause anovulation and amenorrhea. Generally, these are accompanied by abnormal negative feedback between estradiol and the gonadotrophins; coexistence of low estradiol and luteinizing hormone/follicle-stimulating hormone. There are three main causes: (1) genetic diseases that interfere with the migration of GnRH cells into the brain or result in misfolding of GnRH; (2) input from the brain that interrupts normal feedback (e.g. stress and weight loss amenorrhea); and (3) the effect of agents which alter central neurotransmission and hypothalamic function (e.g. elevated prolactin and psychotropic medications). All types of hypothalamic insufficiency result in insufficient stimulation of the ovaries. In addition to amenorrhea, this central alteration also results in other complications (downstream disease) that make hypothalamic amenorrhea of greater consequence than simply reproductive failure. Thus, there may be more at stake in the diagnosis and treatment of hypothalamic failure than brings the patient to her caregiver.
现代诊断方法使区分下丘脑衰竭和卵巢衰竭成为常规。下丘脑促性腺激素释放激素(GnRH)→垂体促性腺激素→卵巢类固醇和抑制素→下丘脑/垂体的有序进展失败导致无排卵/闭经。调节 GnRH 脉冲模式和幅度的下丘脑连接具有可塑性,并对外界/心理条件和内部/代谢因素作出反应,这些因素可能会影响雌激素水平可以作用的下丘脑基质。我们追溯了卵巢周期的神经内分泌调节,重点关注下丘脑连接,这些连接是 GnRH 负反馈和正反馈控制的基础,以及腺垂体的互补作用。调节这个“中枢轴”和子宫内膜发育的主要激素是雌二醇,它从发育中的卵巢卵泡中输出,从而与卵泡发育闭合反馈环。孕激素和抑制素也参与其中。神经内分泌对内部和外部因素的反应会导致无排卵和闭经。通常,这些都会伴随着雌二醇和促性腺激素之间的异常负反馈;低雌二醇和促黄体生成素/卵泡刺激素共存。主要有三个原因:(1)干扰 GnRH 细胞进入大脑的遗传疾病或导致 GnRH 错误折叠;(2)来自大脑的输入中断正常反馈(例如,应激和体重减轻性闭经);(3)改变中枢神经递质传递和下丘脑功能的药物的影响(例如,催乳素升高和精神药物)。所有类型的下丘脑不足都会导致卵巢刺激不足。除了闭经外,这种中枢改变还会导致其他并发症(下游疾病),使下丘脑性闭经的后果不仅仅是生殖功能衰竭。因此,与患者就诊的护理人员相比,诊断和治疗下丘脑衰竭可能涉及更多利害关系。