Prolactin disorders

Niamh Martin
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Abstract

Hyperprolactinaemia can be physiological, pathological or drug induced. Elevated serum prolactin concentrations can cause secondary hypogonadism via inhibition of hypothalamic gonadotropin-releasing hormone and pituitary gonadotropins. Therefore, it is important to determine the pathological causes of hyperprolactinaemia, particularly prolactinoma. Female patients can present with galactorrhoea, menstrual irregularity and infertility, whereas male patients can present with symptoms of secondary hypogonadism. Notably, postmenopausal women and men often present with mass effects secondary to a large macroprolactinoma. Macroprolactin, representing <5% of circulating prolactin, is a polymeric form of prolactin with limited bioavailability and bioactivity. Macroprolactinaemia should be suspected in individuals with a raised prolactin concentration who lack typical features of hyperprolactinaemia. After confirming an elevated serum prolactin and excluding other physiological and pathological causes, pituitary magnetic resonance imaging should be performed to investigate the presence of a prolactinoma or non-prolactinoma pituitary tumour. Bromocriptine and cabergoline are the two dopamine agonists most commonly used to correct abnormal serum prolactin concentrations. Both cause tumour shrinkage in prolactinomas and restore gonadal function and fertility, but cabergoline is preferred as it is more effective and better tolerated. Although there are more safety data for bromocriptine than cabergoline, both are considered to be safe in pregnancy.
催乳激素紊乱
高泌乳素血症可由生理性、病理性或药物引起。血清催乳素浓度升高可通过抑制下丘脑促性腺激素释放激素和垂体促性腺激素引起继发性性腺功能减退。因此,确定高泌乳素血症,特别是泌乳素瘤的病理原因是很重要的。女性患者可表现为溢乳、月经不调、不孕症,而男性患者可表现为继发性性腺功能减退。值得注意的是,绝经后的女性和男性经常出现继发于大催乳素瘤的肿块效应。巨催乳素占循环催乳素的5%,是催乳素的聚合形式,生物利用度和生物活性有限。催乳素浓度升高而缺乏高催乳素血症的典型特征的个体应怀疑有大量催乳素血症。在确认血清催乳素升高并排除其他生理和病理原因后,应进行垂体磁共振成像检查是否存在催乳素瘤或非催乳素瘤垂体肿瘤。溴隐亭和卡麦角林是两种多巴胺激动剂,最常用于纠正血清催乳素浓度异常。这两种药物都能导致催乳素瘤的肿瘤缩小,恢复性腺功能和生育能力,但卡麦角林更有效,耐受性更好。尽管溴隐亭的安全性数据比卡麦角林多,但两者都被认为是安全的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
1.10
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