Petersenn S, Newell-Price J, Findling J W, Gu F, Maldonado M, Sen K, Salgado L R, Colao A, Biller B M K
ENDOC Center for Endocrine Tumors, Hamburg, Germany.
Clin Endocrinol (Oxf). 2014 Feb;80(2):261-9. doi: 10.1111/cen.12259. Epub 2013 Jul 15.
Twenty-four-hour urinary free cortisol (UFC) sampling is commonly used to evaluate Cushing's syndrome. Because there are few data on UFC variability in patients with active Cushing's disease, we analysed baseline UFC in a large patient cohort with moderate-to-severe Cushing's disease and assessed whether variability correlates with hypercortisolism severity. These data will help clinicians establish the minimum number of UFC samples required to obtain reliable data.
Observational study (enrolment phase of Phase III study).
Patients (n = 152) with persistent/recurrent or de novo Cushing's disease and mean UFC (mUFC) ≥1·5×ULN (normal: 30-145 nmol/24 h) were included. Mean UFC level was calculated from four 24-h urine samples collected over 2 weeks.
Over 600 24-h UFC samples were analysed. The mUFC levels of samples 1 and 2 and samples 3 and 4 were 1000 nmol/24 h (SD 1872) and 940 nmol/24 h (SD 2148), respectively; intrapatient coefficient of variation (CV) was 38% for mUFC. The intrapatient CV using all four samples was 52% (95% CI: 48-56). The intrapatient CV was 51% (95% CI: 44-58) for samples 1 and 2, 49% (95% CI: 43-56) for samples 3 and 4 and 54% (95% CI: 49-59) for samples 1, 2 and 3. Variability in mUFC increased as UFC levels increased. There were no correlations between UFC and clinical features of hypercortisolism.
There is intrapatient variability of approximately 50% in 24-h UFC measurements, which is relevant to targets set to estimate any treatment effect. Analysing more than two 24-h collection periods in individual patients does not result in a relevant decrease in variability. Interestingly, UFC levels did not correlate with hypercortisolism severity.
24小时尿游离皮质醇(UFC)采样常用于评估库欣综合征。由于关于活动性库欣病患者UFC变异性的数据较少,我们分析了一大组中重度库欣病患者的基线UFC,并评估变异性是否与皮质醇增多症的严重程度相关。这些数据将有助于临床医生确定获得可靠数据所需的UFC样本的最少数量。
观察性研究(III期研究的入组阶段)。
纳入持续性/复发性或初发性库欣病且平均UFC(mUFC)≥1.5×ULN(正常:30 - 145 nmol/24小时)的患者(n = 152)。平均UFC水平由在2周内收集的4份24小时尿液样本计算得出。
分析了600多个24小时UFC样本。样本1和2以及样本3和4的mUFC水平分别为1000 nmol/24小时(标准差1872)和940 nmol/24小时(标准差2148);mUFC的患者内变异系数(CV)为38%。使用全部4个样本时患者内CV为52%(95%置信区间:48 - 56)。样本1和2的患者内CV为51%(95%置信区间:44 - 58),样本3和4为49%(95%置信区间:43 - 56),样本1、2和3为54%(95%置信区间:49 - 59)。mUFC的变异性随UFC水平升高而增加。UFC与皮质醇增多症的临床特征之间无相关性。
24小时UFC测量中患者内变异性约为50%,这与为评估任何治疗效果所设定的目标相关。在个体患者中分析超过两个24小时收集期并不会使变异性显著降低。有趣的是,UFC水平与皮质醇增多症的严重程度无关。