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Reproducibility of nighttime salivary cortisol and its use in the diagnosis of hypercortisolism compared with urinary free cortisol and overnight dexamethasone suppression test

机译:与尿游离皮质醇和夜间地塞米松抑制试验相比,夜间唾液皮质醇的再现性及其在诊断皮质醇增多症中的应用

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摘要

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. RESULTS: 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%. CONCLUSION: 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.
机译:背景/方法:夜间唾液皮质醇(NSC)被认为是库欣综合症(CS)的有用诊断测试。在没有有关其日常变异性的公开数据的情况下,我们通过在健康志愿者中进行重复测量来评估NSC的可重复性。将其诊断性能与24小时尿游离皮质醇(UFC)和1 mg过夜地塞米松抑制试验在12例CS患者,20例健康志愿者,14例被排除CS或没有明确确定的转诊患者,16例肥胖患者和怀孕后期有20名妇女。结果:NSC在健康志愿者中表现出较高的可重复性,且日常变异性较低,这反映在组内相关系数为0.78上。接受者工作特征曲线的估计临界值为6.1 nmol /升(0.22 microg / dl),在诊断中显示出100%的敏感性和特异性(接受者工作特征曲线下的面积为1.0; 95%置信区间为0.94-1.0)。的CS。 NSC,24小时UFC [在将当地实验室临界值调整为504 nmol / d(183 microg / d)之后,尿皮质醇/肌酐比值显示出在正确识别CS方面优于1 mg地塞米松抑制试验的趋势。在妊娠晚期,唾液皮质醇水平较高时保留的昼夜变化将NSC的特异性降低到75%。结论:基于其卓越的可重复性,易行的非侵入性性质以及至少相似的诊断性能,NSC似乎是24小时UFC的首选替代品,作为CS的一线筛查测试。 NSC,24小时UFC和尿皮质醇/肌酐之比的临界值必须使用足够大的人群的测定方法和中心特异性参考范围进行仔细调整。

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