Viardot Alexander, Huber Peter, Puder Jardena J, Zulewski Henryk, Keller Ulrich, Müller Beat
Clinic for Endocrinology, Diabetes, and Clinical Nutrition, University Hospital Basel, Switzerland.
J Clin Endocrinol Metab. 2005 Oct;90(10):5730-6. doi: 10.1210/jc.2004-2264. Epub 2005 Jul 12.
BACKGROUND/METHODS: Nighttime salivary cortisol (NSC) has been suggested to be a useful diagnostic test for Cushing's syndrome (CS). In the absence of published data on its day-to-day variability, we assessed the reproducibility of NSC by repeated measurements in healthy volunteers. Its diagnostic performance was compared with 24-h urinary free cortisol (UFC) and 1 mg overnight dexamethasone suppression test in 12 patients with CS, 20 healthy volunteers, 14 referred patients in which CS was excluded or not firmly established, 16 obese patients, and 20 women in late pregnancy.
NSC showed a superior reproducibility in healthy volunteers with a low day-to-day variability as reflected by an intraclass correlation coefficient of 0.78. The receiver operating characteristic curve-estimated cutoff of 6.1 nmol/liter (0.22 microg/dl) demonstrated a sensitivity and specificity of 100% (area under the receiver operating characteristic curve, 1.0; 95% confidence interval, 0.94-1.0) in the diagnosis of CS. NSC, 24-h UFC [after adjusting the local laboratory cutoff to 504 nmol/d (183 microg/d)], and the urinary cortisol/creatinine ratio showed a tendency to be superior to 1 mg dexamethasone suppression test in correctly identifying CS. In late pregnancy, the preserved diurnal variation at a higher level of salivary cortisol reduced the specificity of NSC to 75%.
Based on its remarkable reproducibility, easy noninvasive nature, and at least similar diagnostic performance, NSC appears to be a preferable alternative to 24-h UFC as a first-line screening test for CS. The cutoff values of NSC, 24-h UFC, and urinary cortisol/creatinine ratio have to be carefully adjusted using assay and center-specific reference ranges of sufficiently large populations.
背景/方法:夜间唾液皮质醇(NSC)已被认为是库欣综合征(CS)的一种有用的诊断测试。由于缺乏关于其每日变异性的已发表数据,我们通过对健康志愿者进行重复测量来评估NSC的可重复性。在12例CS患者、20名健康志愿者、14例排除或未确诊CS的转诊患者、16例肥胖患者和20例妊娠晚期妇女中,将其诊断性能与24小时尿游离皮质醇(UFC)和1毫克过夜地塞米松抑制试验进行了比较。
NSC在健康志愿者中显示出较高的可重复性,每日变异性较低,组内相关系数为0.78。受试者工作特征曲线估计的截断值为6.1纳摩尔/升(0.22微克/分升),在CS诊断中显示出100%的敏感性和特异性(受试者工作特征曲线下面积,1.0;95%置信区间,0.94 - 1.0)。NSC、24小时UFC[将当地实验室截断值调整为504纳摩尔/天(183微克/天)后]以及尿皮质醇/肌酐比值在正确识别CS方面倾向于优于1毫克地塞米松抑制试验。在妊娠晚期,唾液皮质醇水平较高时昼夜变化的保留将NSC的特异性降低至75%。
基于其显著的可重复性、简便的非侵入性性质以及至少相似的诊断性能,NSC似乎是作为CS一线筛查试验替代24小时UFC的更优选择。NSC、24小时UFC和尿皮质醇/肌酐比值的截断值必须使用足够大人群的测定法和特定中心的参考范围进行仔细调整。