Buchfelder M, Fahlbusch R, Wentzlaff-Eggebert H, Brabant G, Stalla G K, Müller O A
Neurochirurgische Klinik, Universität Erlangen-Nürnberg, Germany.
J Clin Endocrinol Metab. 1993 Sep;77(3):720-4. doi: 10.1210/jcem.77.3.8396575.
The endocrinological, surgical, and histological findings of patients with ACTH-dependent Cushing's disease were correlated with the pulsatile secretion pattern of ACTH and cortisol and the outcome after transsphenoidal pituitary surgery. A total of 28 patients were studied. The preoperative pulsatile secretion of ACTH and cortisol was assessed by sampling blood at 20-min intervals over 24 h. The pulsatile pattern of secretion was analyzed by the Cluster program. In 21 patients, an ACTH-secreting pituitary adenoma was identified and resected. Of these patients, 18 underwent clinical remission, and their cortisol secretion was suppressed to a normal level by low dose dexamethasone. Histological examinations in the patients with persistent disease revealed normal pituitary in 6 cases, nodular hyperplasia in 1, and ACTH-secreting pituitary adenoma in 3 cases. Analysis of the pulsatile pattern of ACTH and cortisol secretion did not reveal significant differences in timing, frequency, and/or amplitude of ACTH and cortisol pulses in normalized patients and those with persistent disease after surgery. It is concluded that analysis of the secretory pattern is not a suitable method for predicting the outcome of transsphenoidal surgery in patients with ACTH-dependent Cushing's disease.
促肾上腺皮质激素(ACTH)依赖性库欣病患者的内分泌、手术及组织学检查结果与ACTH和皮质醇的脉冲分泌模式以及经蝶窦垂体手术后的结果相关。共研究了28例患者。术前通过在24小时内每隔20分钟采集一次血样来评估ACTH和皮质醇的脉冲分泌情况。分泌的脉冲模式通过Cluster程序进行分析。21例患者中发现并切除了分泌ACTH的垂体腺瘤。其中18例患者实现临床缓解,其皮质醇分泌被低剂量地塞米松抑制至正常水平。对疾病持续存在患者的组织学检查显示,6例垂体正常,1例结节性增生,3例为分泌ACTH的垂体腺瘤。对ACTH和皮质醇分泌脉冲模式的分析未发现术后病情缓解患者与疾病持续存在患者在ACTH和皮质醇脉冲的时间、频率和/或幅度方面存在显著差异。得出结论,分泌模式分析并非预测ACTH依赖性库欣病患者经蝶窦手术结果的合适方法。