Veldman R G, Frölich M, Pincus S M, Veldhuis J D, Roelfsema F
Department of Endocrinology and Metabolic Diseases, Leiden University Medical Center, The Netherlands.
J Clin Endocrinol Metab. 2000 Nov;85(11):4039-46. doi: 10.1210/jcem.85.11.6967.
ACTH production in Cushing's disease is characterized by a markedly elevated rate of basal (nonpulsatile) secretion, an increased mass of ACTH released per burst and an unremarkable pulse frequency. In addition, the ACTH secretory process and that of GH and PRL exhibit profoundly disordered patterns. Whether some or all of these disturbances can be reversed or normalized by transsphenoidal microadenomectomy remains unknown. We therefore investigated the detailed dynamics of ACTH, GH, and PRL in eight patients (aged 38.9+/-4.2 yr) with pituitary-dependent Cushing's disease who were in long-term (8.2+/-1.7 yr) clinical remission following transsphenoidal surgery and eight controls matched for age, gender, and body mass index. To this end, blood was sampled at 10-min intervals for 24 h for the later assay of ACTH, cortisol, GH, and PRL. Secretory activity was quantitated by deconvolution methods, and the pattern orderliness (regularity) of hormone release was determined by the approximate entropy (ApEn) statistic. The joint synchrony of ACTH and cortisol secretion was monitored by the cognate bivariate statistic, cross-ApEn. Diurnal properties of the hormonal release were appraised by cosinor analysis. Based on deconvolution analysis, postsurgical patients exhibited a normal frequency, half-life, duration, and mass of ACTH and cortisol secretory bursts. Accordingly, the 24-h production rates of both ACTH (2.5+/-0.7 microg/L in patients vs. 2.9+/-0.7 microg/L in controls; P = 0.755) and cortisol (49+/-11 micromol/L in patients vs. 73+/-15 micromol/L in controls; P = 0.217) were normal also. The acrophase of the diurnal rhythm of ACTH (patients, 0817 h +/- 37 min; controls, 0850 h +/- 38 min; P = 0.629) and cortisol (patients, 1000 h +/- 24 min; controls, 0855 h +/- 30 min; P = 0.175) was also restored by surgery. ApEn values of ACTH (patients, 1.168 +/- 0.090; controls, 0.864+/-0.122; P = 0.133) and cross-ApEn of ACTH-cortisol (patients, 1.396+/-0.087; controls, 1.170+/-0.076; P = 0.140) secretion were both normal in this cohort, denoting restoration of the secretory process regularity. Cortisol ApEn was slightly higher in patients (patients, 1.034+/-0.084; controls, 0.831+/-0.038; P = 0.048). Both GH and PRL time series manifested full reconstitution of pulsatile, 24-h rhythmic, and entropic properties. In summary, clinically successful transsphenoidal microadenomectomy in adults with Cushing's disease can fully normalize virtually all quantitative features of regulated ACTH, cortisol, GH, and PRL secretion. Further studies will be needed to establish the consistency of these findings in larger cohorts of adults with Cushing's disease and in children with this disorder and to delineate the significance, if any, of a residual, minimally detectable disruption of orderly cortisol secretion in this patient population.
库欣病中促肾上腺皮质激素(ACTH)的分泌具有以下特点:基础(非脉冲式)分泌速率显著升高、每次脉冲释放的ACTH量增加以及脉冲频率无明显变化。此外,ACTH的分泌过程与生长激素(GH)和催乳素(PRL)的分泌过程呈现出严重紊乱的模式。经蝶窦微腺瘤切除术能否逆转或使这些紊乱中的部分或全部恢复正常仍不清楚。因此,我们研究了8例垂体依赖性库欣病患者(年龄38.9±4.2岁)的ACTH、GH和PRL的详细动态变化,这些患者经蝶窦手术后处于长期(8.2±1.7年)临床缓解期,并与8例年龄、性别和体重指数相匹配的对照组进行了比较。为此,每隔10分钟采集一次血样,共采集24小时,用于后续ACTH、皮质醇、GH和PRL的检测。通过去卷积方法对分泌活性进行定量,并通过近似熵(ApEn)统计量确定激素释放的模式有序性(规律性)。通过相关双变量统计量交叉ApEn监测ACTH和皮质醇分泌的联合同步性。通过余弦分析评估激素释放的昼夜特性。基于去卷积分析,术后患者的ACTH和皮质醇分泌脉冲的频率、半衰期、持续时间和量均正常。因此,ACTH(患者为2.5±0.7μg/L,对照组为2.9±0.7μg/L;P = 0.755)和皮质醇(患者为49±11μmol/L,对照组为73±15μmol/L;P = 0.217)的24小时分泌率也正常。手术也恢复了ACTH(患者为0817 h±37分钟,对照组为0850 h±38分钟;P = 0.629)和皮质醇(患者为1000 h±24分钟,对照组为0855 h±30分钟;P = 0.175)昼夜节律的峰值相位。该队列中ACTH的ApEn值(患者为1.168±0.090,对照组为0.864±0.122;P = 0.133)和ACTH - 皮质醇的交叉ApEn值(患者为1.396±0.087,对照组为1.170±0.076;P = 0.140)均正常,表明分泌过程的规律性得以恢复。患者的皮质醇ApEn值略高(患者为1.034±0.084,对照组为0.831±0.038;P = 0.048)。GH和PRL的时间序列均显示出脉冲式、24小时节律性和熵特性的完全重建。总之,对于成年库欣病患者,临床上成功的经蝶窦微腺瘤切除术几乎可以使受调节的ACTH、皮质醇、GH和PRL分泌的所有定量特征完全正常化。需要进一步研究以确定这些发现在更大规模的成年库欣病患者队列以及患有该疾病的儿童中的一致性,并确定在该患者群体中残留的、最小可检测到的有序皮质醇分泌紊乱(若有的话)的意义。