Department of Clinical Sciences and Community Health, University of Milan, Istituto Auxologico Italiano, Piazzale Brescia 40, 20149 Milan, Italy.
J Clin Endocrinol Metab. 2012 Oct;97(10):3577-83. doi: 10.1210/jc.2012-2328. Epub 2012 Jul 31.
Cushing's disease, i.e. cortisol excess due to an ACTH-secreting pituitary adenoma, is a rare disorder with considerable morbidity and mortality but no satisfactory medical treatment as yet. Experimental data have recently shown that retinoic acid restrains ACTH secretion by tumoral corticotropes.
Our objective was to evaluate the efficacy and safety profile of retinoic acid treatment in patients with Cushing's disease.
This is a prospective, multicenter study. Seven patients with Cushing's disease (three men, four postmenopausal women) were started on 10 mg retinoic acid daily and dosage increased up to 80 mg daily for 6-12 months. ACTH, urinary free cortisol (UFC), and serum cortisol as well as clinical features of hypercortisolism and possible side effects of retinoic acid were evaluated at baseline, during retinoic acid administration, and after drug withdrawal.
A marked decrease in UFC levels was observed in five patients; mean UFC levels on retinoic acid were 22-73% of baseline values and normalization in UFC was achieved in three patients. Plasma ACTH decreased in the first month of treatment and then returned to pretreatment levels in responsive patients whereas no clear-cut pattern could be detected for serum cortisol. Blood pressure, glycemia, and signs of hypercortisolism, e.g. body weight and facial plethora, were ameliorated to a variable extent on treatment. Patients reported only mild adverse effects, e.g. xerophthalmia and arthralgias.
Long-term treatment with retinoic acid proved beneficial and well tolerated in five of seven patients with Cushing's disease. This represents a novel, promising approach to medical treatment in Cushing's disease.
库欣病,即由于 ACTH 分泌性垂体腺瘤导致的皮质醇过多,是一种罕见的疾病,发病率和死亡率都很高,但目前尚无令人满意的治疗方法。最近的实验数据表明,维甲酸可抑制肿瘤促皮质素细胞分泌 ACTH。
我们的目的是评估维甲酸治疗库欣病患者的疗效和安全性。
这是一项前瞻性、多中心研究。7 例库欣病患者(3 名男性,4 名绝经后女性)开始每日服用 10mg 维甲酸,6-12 个月内剂量增加至每日 80mg。在基线、维甲酸治疗期间和停药后评估 ACTH、尿游离皮质醇(UFC)和血清皮质醇以及皮质醇过多的临床特征和维甲酸可能的副作用。
5 例患者 UFC 水平明显下降;维甲酸治疗期间 UFC 平均水平为基线值的 22-73%,3 例患者 UFC 水平正常化。治疗后第 1 个月血浆 ACTH 下降,随后在有反应的患者中恢复至治疗前水平,而血清皮质醇则无明显模式。血压、血糖和皮质醇过多的体征,如体重增加和面部充血,在治疗过程中得到不同程度的改善。患者仅报告轻微的不良反应,如干眼症和关节痛。
在 7 例库欣病患者中,有 5 例患者长期使用维甲酸治疗效果良好且耐受良好。这代表了库欣病治疗的一种新的、有前途的方法。