催乳素瘤妇女高雄激素血症的评价

IF 0.2 Q4 ENDOCRINOLOGY & METABOLISM
M. Ünal, Z. Karaca, K. Ünlühızarcı, F. Keleştemur
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Further, adrenocorticotropin stimulation test was performed to analyze cortisol, dehydroepiandrosterone sulfate (DHEAS), androstenedione, 11-deoxycortisol (11-S), and 17-hydroxyprogesterone (17-OHP) responses. Results: A significantly higher level of prolactin compared to the control group was seen in prolactinoma patients, which reverted to normal levels after cabergoline treatment. Estradiol (E2) concentration was lower in patients with prolactinoma than control group and it did not show a significant increase after being treated with cabergoline. Patients with prolactinoma exhibited decreased sex hormone-binding globulin (SHBG) concentration in blood, which also increased significantly after the treatment. The levels of basal androstenedione, DHEAS, 17-OH progesterone, 11-S, and cortisol were found to be similar between the two groups. Basal and stimulated DHEAS and androstenedione levels decreased significantly after cabergoline treatment in prolactinoma patients. 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引用次数: 0

摘要

目的:高催乳素血症对雄激素过多障碍的鉴别诊断。然而,在临床实践中,催乳素水平升高(高催乳素血症)是高雄激素血症的一个非常罕见的原因。本研究旨在探讨卡麦角林治疗前后催乳素瘤女性患者是否存在高雄激素症/高雄激素血症。材料和方法:20名最近被诊断为泌乳素瘤的妇女和15名年龄在18至50岁之间的健康妇女参加了这项研究。在基线和卡麦角林治疗6个月后对患者进行评估。仔细记录患者的任何体征和症状高雄激素血症和雄激素浓度在血液中。进一步,进行促肾上腺皮质激素刺激试验,分析皮质醇、硫酸脱氢表雄酮(DHEAS)、雄烯二酮、11-脱氧皮质醇(11-S)和17-羟基孕酮(17-OHP)的反应。结果:催乳素瘤患者催乳素水平明显高于对照组,经卡麦角林治疗后恢复正常。催乳素瘤患者雌二醇(E2)浓度低于对照组,经卡麦角林治疗后雌二醇(E2)浓度无明显升高。催乳素瘤患者血液中性激素结合球蛋白(SHBG)浓度降低,治疗后也显著升高。基础雄烯二酮、DHEAS、17-OH孕酮、11-S和皮质醇水平在两组之间相似。卡麦角林治疗后催乳素瘤患者的基础和刺激DHEAS和雄烯二酮水平显著降低。痤疮、多毛和雄激素性脱发的存在在两组中相似。9例催乳素瘤患者盆腔超声检查显示多囊卵巢(PCO),发生率明显高于对照组。9例PCO患者中,3例经治疗后卵巢形态恢复正常。结论:高催乳素血症可能不会导致临床上显著的高雄激素血症和多毛症。此外,高泌乳素血症的治疗没有导致多毛症患者评分的显著改善,如果存在的话。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of Hyperandrogenemia in Women with Prolactinoma
Objective: Differential diagnosis of androgen excess disorders revealed the occurrence of hyperprolactinemia. However, an elevated level of prolactin (hyperprolactinemia) is a very infrequent cause of hyperandrogenemia in clinical practice. This study aimed to investigate the presence of hyperandrogenism/hyperandrogenemia in women with prolactinoma before and after treatment with cabergoline. Material and Methods: Twenty women diagnosed with prolactinoma in the recent past and 15 healthy women between the ages of 18 to 50 were enrolled in the study. Patients were evaluated at the baseline and after six months of cabergoline treatment. Patients were carefully noted for any signs and symptoms of hyperandrogenemia and concentration of androgen in blood. Further, adrenocorticotropin stimulation test was performed to analyze cortisol, dehydroepiandrosterone sulfate (DHEAS), androstenedione, 11-deoxycortisol (11-S), and 17-hydroxyprogesterone (17-OHP) responses. Results: A significantly higher level of prolactin compared to the control group was seen in prolactinoma patients, which reverted to normal levels after cabergoline treatment. Estradiol (E2) concentration was lower in patients with prolactinoma than control group and it did not show a significant increase after being treated with cabergoline. Patients with prolactinoma exhibited decreased sex hormone-binding globulin (SHBG) concentration in blood, which also increased significantly after the treatment. The levels of basal androstenedione, DHEAS, 17-OH progesterone, 11-S, and cortisol were found to be similar between the two groups. Basal and stimulated DHEAS and androstenedione levels decreased significantly after cabergoline treatment in prolactinoma patients. The presence of acne, hirsutism, and androgenic alopecia were similar in both groups. Pelvic ultrasonography revealed polycystic ovary (PCO) in nine patients with prolactinoma, which was significantly more frequent than in the control group. Among the 9 PCO patients, normal ovarian morphology was restored in three patients after the treatment. Conclusion: From the data, it may be suggested that hyperprolactinemia may not lead to clinically significant hyperandrogenemia and hirsutism. Moreover, the treatment of hyperprolactinemia does not lead to significant improvement in hirsutism score of the patients, if exists.
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