Department of Endocrinology, University Hospitals of Leicester, Leicester, UK.
Department of Endocrinology, University of Leicester, Leicester, UK.
Clin Endocrinol (Oxf). 2021 Aug;95(2):229-238. doi: 10.1111/cen.14399. Epub 2021 Jan 11.
Functional hypothalamic amenorrhoea (FHA) is a common form of secondary amenorrhoea without an identifiable structural cause. Suppression of gonadotrophin-releasing hormone (GnRH) pulsatility results in reduced luteinizing hormone (LH) levels, with subsequent reduction in oestradiol, anovulation and cessation of menstruation. GnRH pulsatility suppression is a recognized complication of psychological stress, disordered eating, low body weight, excessive exercise or a combination of these factors.
Individuals with FHA demonstrate low energy availability (EA), body fat percentage and energy expenditure. Documented adipocytokine changes notably, raised adiponectin, ghrelin, PYY, and decreased leptin, are associated with GnRH suppression. Other endocrine responses seen in this low EA state include low insulin levels, low total T3, increased basal cortisol levels and a reduced response to corticotrophin-releasing hormone (CRH) administration. FHA is associated with raised growth hormone (GH) and low insulin-like growth factor (IGF-1), suggesting relative GH resistance. Kisspeptins are a group of polypeptides, recently discovered to play a major role in the regulation of the reproductive axis through influencing GnRH release. KNDy (kisspeptin/neurokinin B/dynorphin) act on GnRH neurons and a multitude of factors result in their release.
Management of FHA is imperative to prevent adverse outcomes in bone density, cardiovascular risk profile, psychological well-being and fertility. Outwith modification of nutritional intake and exercise, limited therapeutic strategies are currently available for women with FHA. Advancements in the understanding of the pathophysiological basis of this under-recognized and under-treated clinical entity will aid management and may result in the development of novel therapeutic approaches.
功能性下丘脑性闭经(FHA)是一种常见的继发性闭经形式,没有可识别的结构原因。促性腺激素释放激素(GnRH)脉冲发生器的抑制导致黄体生成素(LH)水平降低,随后雌激素降低,无排卵和月经停止。 GnRH 脉冲发生器抑制是心理压力、饮食失调、低体重、过度运动或这些因素的组合的公认并发症。
FHA 的发病机制: FHA 患者表现出低能量可用性(EA)、体脂肪百分比和能量消耗。记录到的脂肪细胞因子变化显著,升高的脂联素、胃饥饿素、PYY 和降低的瘦素与 GnRH 抑制有关。在这种低 EA 状态下观察到的其他内分泌反应包括胰岛素水平低、总 T3 低、基础皮质醇水平升高和促肾上腺皮质激素释放激素(CRH)给药后的反应降低。FHA 与升高的生长激素(GH)和低胰岛素样生长因子(IGF-1)有关,表明存在相对的 GH 抵抗。 Kisspeptins 是一组多肽,最近发现它们在通过影响 GnRH 释放来调节生殖轴方面发挥主要作用。KNDy(kisspeptin/neurokinin B/dynorphin)作用于 GnRH 神经元,多种因素导致它们的释放。
FHA 的管理对于预防骨密度、心血管风险状况、心理健康和生育能力的不良后果至关重要。除了营养摄入和运动的改变外,目前对于 FHA 患者可用的治疗策略有限。对这种未被充分认识和治疗不足的临床实体的病理生理基础的理解的进展将有助于管理,并可能导致新的治疗方法的开发。