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库欣病患者长期使用丙戊酸钠治疗失败。

Failure of long-term therapy with sodium valproate in Cushing's disease.

作者信息

Colao A, Pivonello R, Tripodi F S, Orio F, Ferone D, Cerbone G, Di Somma C, Merola B, Lombardi G

机构信息

Department of Molecular and Clinical Endocrinology and Oncology, Federico II University, Napoli, Italy.

出版信息

J Endocrinol Invest. 1997 Jul-Aug;20(7):387-92. doi: 10.1007/BF03347989.

Abstract

The aim of the current study was to evaluate the effectiveness of a long-term treatment with sodium valproate in 19 patients with Cushing's disease. Before therapy beginning, the patients were subjected to acute test with 600 mg sodium valproate. Then, they were subjected to a 3-month therapy with sodium valproate at the dose of 600 mg/day before surgery (presurgical study). The 7 patients not surgically cured were subjected again to a 3-month therapy with sodium valproate at the dose of 600 mg/day after surgery (postsurgical study). Circulating ACTH and cortisol and urinary free cortisol levels were evaluated before and monthly after the beginning of the therapy. A decrease of plasma ACTH and serum cortisol levels greater than 50% of baseline was considered as positive response to acute test whereas the normalization of plasma ACTH, serum cortisol and urinary free cortisol levels and the clinical remission were considered as positive response to the long-term treatment. At acute test, 8 patients were considered responders and 11 patients non-responders. In no patient plasma ACTH, serum cortisol and urinary free cortisol were normalized during the long-term treatment. Urinary free cortisol levels significantly decreased (483.2 +/- 33.8 vs 699.4 +/- 67.0 micrograms/24 h), whereas plasma ACTH (302.8 +/- 17.7 vs 183.3 +/- 25.0 ng/l) and serum cortisol (466.5 +/- 23.2 vs 356.7 +/- 19.6 micrograms/l) significantly increased during sodium valproate administration in the 19 patients enrolled in the presurgical study. Plasma ACTH (247.7 +/- 22.3 vs 168.6 +/- 15.0 ng/l), serum cortisol (387.4 +/- 35.8 vs 282.0 +/- 16.0 micrograms/l) and urinary free cortisol (370.9 +/- 70.6 vs 261.3 +/- 37.8 micrograms/24 h) levels significantly increased in the 7 patients enrolled in the postsurgical study. No patient had clinical remission of Cushing's disease. In conclusion, the current study showed that long-term therapy with sodium valproate is not useful in the therapeutic management of Cushing's disease neither as alternative nor as adjunctive therapy to surgery.

摘要

本研究的目的是评估丙戊酸钠长期治疗对19例库欣病患者的有效性。在治疗开始前,患者接受了600毫克丙戊酸钠的急性试验。然后,他们在手术前接受了为期3个月、剂量为600毫克/天的丙戊酸钠治疗(术前研究)。7例手术未治愈的患者在术后再次接受了为期3个月、剂量为600毫克/天的丙戊酸钠治疗(术后研究)。在治疗开始前及开始后每月评估循环促肾上腺皮质激素(ACTH)、皮质醇和尿游离皮质醇水平。血浆ACTH和血清皮质醇水平下降超过基线水平的50%被视为对急性试验的阳性反应,而血浆ACTH、血清皮质醇和尿游离皮质醇水平的正常化以及临床缓解被视为对长期治疗的阳性反应。在急性试验中,8例患者被视为反应者,11例患者被视为无反应者。在长期治疗期间,没有患者的血浆ACTH、血清皮质醇和尿游离皮质醇水平恢复正常。在术前研究的19例患者中,丙戊酸钠给药期间尿游离皮质醇水平显著下降(483.2±33.8 vs 699.4±67.0微克/24小时),而血浆ACTH(302.8±17.7 vs 183.3±25.0纳克/升)和血清皮质醇(466.5±23.2 vs 356.7±19.6微克/升)显著升高。在术后研究的7例患者中,血浆ACTH(247.7±22.3 vs 168.6±15.0纳克/升)、血清皮质醇(387.4±35.8 vs 282.0±16.0微克/升)和尿游离皮质醇(370.9±70.6 vs 261.3±37.8微克/24小时)水平显著升高。没有患者出现库欣病的临床缓解。总之,本研究表明,丙戊酸钠长期治疗对库欣病的治疗管理无效,既不能作为手术的替代疗法,也不能作为辅助疗法。

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