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纳曲酮治疗可恢复体重减轻相关闭经患者的月经周期。

Naltrexone treatment restores menstrual cycles in patients with weight loss-related amenorrhea.

作者信息

Genazzani A D, Petraglia F, Gastaldi M, Volpogni C, Gamba O, Genazzani A R

机构信息

Department of Obstetrics and Gynecology, University of Modena, Italy.

出版信息

Fertil Steril. 1995 Nov;64(5):951-6. doi: 10.1016/s0015-0282(16)57908-4.

DOI:10.1016/s0015-0282(16)57908-4
PMID:7589640
Abstract

OBJECTIVE

To evaluate whether the efficacy of naltrexone administration in patients with hypothalamic amenorrhea correlates to the response to an acute naloxone test.

DESIGN

Thirty patients with hypothalamic amenorrhea associated with weight loss were studied. After naloxone test (4 mg in bolus IV) patients were divided into two groups: group A, nonresponsive (n = 15) and group B, responsive (n = 15). Group A underwent two cycles of hormonal replacement therapy with E2 patches and medroxyprogesterone acetate. Then all patients were administered naltrexone at the dosage 50 mg/d orally for 6 months. A third group of 10 amenorrheic patients were treated with oral placebo with the same schedule.

RESULTS

Plasma gonadal steroid levels increased in all patients and in 24 of 30 patients the menstrual bleeding occurred within 90 days from the beginning of treatment. After 6 months from naltrexone discontinuation, 18 of 24 patients still showed the occurrence of menstrual cycles. Luteinizing hormone plasma levels and LH pulse amplitude increased after 3 months of treatment and remained unchanged 6 months after naltrexone suspension. Plasma FSH levels did not show any change in any patient. The body mass index increased after 3 months in all patients who menstruated. Patients treated with placebo did not show any significant change in gonadotropins and gonadal steroid plasma levels.

CONCLUSIONS

The present study supports the efficacy of naltrexone therapy for patients with hypothalamic amenorrhea either responsive or nonresponsive to naloxone test.

摘要

目的

评估纳曲酮治疗下丘脑性闭经患者的疗效是否与急性纳洛酮试验的反应相关。

设计

对30例伴有体重减轻的下丘脑性闭经患者进行研究。在纳洛酮试验(静脉推注4mg)后,患者被分为两组:A组,无反应组(n = 15)和B组,有反应组(n = 15)。A组接受两个周期的雌激素贴片和醋酸甲羟孕酮激素替代治疗。然后所有患者口服纳曲酮,剂量为50mg/d,持续6个月。第三组10例闭经患者接受相同疗程的口服安慰剂治疗。

结果

所有患者血浆性腺类固醇水平均升高,30例患者中有24例在治疗开始后90天内出现月经出血。停用纳曲酮6个月后,24例患者中有18例仍有月经周期出现。治疗3个月后促黄体生成素血浆水平和促黄体生成素脉冲幅度升高,停用纳曲酮6个月后保持不变。所有患者的血浆促卵泡生成素水平均未显示任何变化。所有月经来潮的患者在3个月后体重指数增加。接受安慰剂治疗的患者促性腺激素和性腺类固醇血浆水平未显示任何显著变化。

结论

本研究支持纳曲酮治疗对纳洛酮试验有反应或无反应的下丘脑性闭经患者的疗效。

相似文献

1
Naltrexone treatment restores menstrual cycles in patients with weight loss-related amenorrhea.纳曲酮治疗可恢复体重减轻相关闭经患者的月经周期。
Fertil Steril. 1995 Nov;64(5):951-6. doi: 10.1016/s0015-0282(16)57908-4.
2
Naltrexone administration modulates the neuroendocrine control of luteinizing hormone secretion in hypothalamic amenorrhoea.纳曲酮的给药可调节下丘脑性闭经中促黄体生成素分泌的神经内分泌控制。
Hum Reprod. 1995 Nov;10(11):2868-71. doi: 10.1093/oxfordjournals.humrep.a135809.
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Even after priming with ovarian steroids or pulsatile gonadotropin-releasing hormone administration, naltrexone is unable to induce ovulation in women with functional hypothalamic amenorrhea.即使在使用卵巢甾体激素进行预处理或脉冲式给予促性腺激素释放激素后,纳曲酮仍无法诱导功能性下丘脑性闭经女性排卵。
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Pulsatile luteinizing hormone secretion in hypothalamic amenorrhea, anorexia nervosa, and polycystic ovarian disease during naltrexone treatment.纳曲酮治疗期间下丘脑性闭经、神经性厌食症和多囊卵巢疾病中促黄体生成素的脉冲式分泌
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Evidence for increased dopaminergic and opioid activity in patients with hypothalamic hypogonadotropic amenorrhea.下丘脑性低促性腺激素性闭经患者多巴胺能和阿片类活性增加的证据。
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[Ovulation induction by the chronic administration of naltrexone in a patient with secondary hypothalamic amenorrhea].[纳曲酮长期给药诱导继发性下丘脑性闭经患者排卵]
Rev Chil Obstet Ginecol. 1992;57(1):39-43.
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Modulatory role of estrogens and progestins on growth hormone episodic release in women with hypothalamic amenorrhea.雌激素和孕激素对下丘脑性闭经女性生长激素脉冲式释放的调节作用。
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Naltrexone in functional hypothalamic amenorrhea and in the normal luteal phase.纳曲酮用于功能性下丘脑性闭经及正常黄体期。
Obstet Gynecol. 1990 Dec;76(6):1115-20.
10
Naltrexone must not be considered a real therapy in functional hypothalamic amenorrhea. The results of a double blind controlled study.
Panminerva Med. 1993 Dec;35(4):214-7.

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