Beneficial effects of high daily dose bromocriptine treatment in Cushing's disease.

L B Mercado-Asis, K Yasuda, M Murayama, T Mune, H Morita, K Miura
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引用次数: 36

Abstract

Treatment with a high daily dose bromocriptine was evaluated in 6 Cushing's disease patients (4 females and 2 males; aged 23 to 56 years). The highest doses administered were 40 mg to patient 1, 55 mg to patient 2, 35 mg to patient 3, 25 mg to patient 4, 25 mg to patient 5, and 17.5 mg to patient 6. The former 3 cases, 2 (patients 1 and 2) of whom were previously reported and further followed up, showed clinical and biochemical improvement with the regimen. Patient 1 who obtained remission with 40 mg/day has been on remission for further 14 months with a total of 36 months. Patient 2, who had a reduction in pituitary tumor size with 35 mg daily, relapsed thereafter. The therapy, however, resolved the paradoxical responses of plasma ACTH and cortisol to arginine. Readministration of bromocriptine resulted into another clinical and biochemical improvement with 45 to 55 mg/day. Patient 3, a relapsed case after a remission with reserpine plus pituitary irradiation, showed an improvement in the 24-h urinary free cortisol excretion with 35 mg/day. Patient 4 was the only case who had a marked decrease in plasma cortisol (basal; 16.3, nadir; 1.9 micrograms/dl) after a single-dose bromocriptine test among the 5 cases tested. The patient had favorable response with 25 mg/day for 2 months but the dose was not increased after an escape. Patient 5 received the drug in 4 occasions, 7.5 to 25 mg/day, in combination with several agents, which failed to induce clinical remission. The last patient did not respond to a maximum dose of 17.5 mg/day. These observations suggest that, regardless of the result of a single-dose bromocriptine test, treatment with a high daily dose of bromocriptine, 35 mg or more, may be necessary to obtain a favorable clinical response and normal cortisol secretion.

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每日大剂量溴隐亭治疗库欣病的有益效果。
对6例库欣病患者(4女2男;年龄在23至56岁之间)。最高剂量为患者1 40毫克,患者2 55毫克,患者3 35毫克,患者4 25毫克,患者5 25毫克,患者6 17.5毫克。前3例,其中2例(患者1、2)均为既往报告并随访,经该方案治疗后临床及生化指标均有改善。患者1以40mg /天获得缓解后,缓解期又持续了14个月,总共36个月。患者2每日服用35mg减小垂体瘤大小,此后复发。然而,该疗法解决了血浆ACTH和皮质醇对精氨酸的矛盾反应。再次给予溴隐亭45 ~ 55 mg/天,临床和生化均有改善。患者3,在利血平加垂体照射缓解后复发的病例,在35 mg/天的治疗下,24小时尿游离皮质醇排泄有所改善。患者4是唯一一例血浆皮质醇(基础;16.3,最低点;1.9微克/分升),经单剂量溴隐亭试验。患者以25mg /天治疗2个月有良好的反应,但在逃逸后没有增加剂量。患者5分4次服用该药,剂量为7.5 ~ 25mg /天,联用多种药物,均未引起临床缓解。最后一名患者对17.5 mg/天的最大剂量没有反应。这些观察结果表明,无论单剂量溴隐亭试验的结果如何,每日高剂量溴隐亭(35mg或更高)的治疗可能需要获得良好的临床反应和正常的皮质醇分泌。
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