Vogeser Michael, Durner Jürgen, Seliger Ewald, Auernhammer Christoph
Institute of Clinical Chemistry, Hospital of the University of Munich, Marchioninistrasse 15, 81377 Munich, Germany.
Clin Chem Lab Med. 2006;44(12):1441-5. doi: 10.1515/CCLM.2006.244.
Measurement of late-night salivary cortisol concentrations is increasingly used as a screening test in suspected Cushing's syndrome. Cortisol concentrations are typically extremely low in late-night samples and discordant assay-specific reference ranges have been reported. Therefore, the aim of our study was to assess the analytical performance of the first automated cortisol immunoassay specified for salivary measurements and to establish late-night sampling reference-range data for this test.
Salivary cortisol was measured using the Roche Cobas Cortisol assay (Roche Diagnostics). Five salivary pools in different concentration ranges were used to assess the inter-assay imprecision of this test in a two-centre evaluation protocol including two reagent lots. Linearity was tested by serial dilution. Salivary samples were obtained at 23:00 h from 100 apparently healthy volunteers using a commercially available salivary sampling device (Salivette, Sarstedt). A subset of 20 samples was used for method comparison with isotope dilution liquid chromatography-tandem mass spectrometry.
Inter-assay coefficients of variation (n=20) between 11.6% and 40.4% were found for mean cortisol concentrations between 12.9 and 2.6 nmol/L, with an estimated functional sensitivity of approximately 5.0 nmol/L. The test also gave linear results in the lowest concentration range between 1.0 and 8.3 nmol/L. Mean late-night salivary cortisol of 5.0 nmol/L was found for healthy individuals; the absolute range was 1.4-16.7 nmol/L, and the 95th percentile was 8.9 nmol/L. Substantially lower concentrations were found with isotope dilution LC-MS/MS compared to immunoassay results (mean concentrations 1.8 and 4.4 nmol/L, respectively).
The automated assay investigated was found to offer acceptable analytical performance in the very low concentration range required for late-night salivary cortisol, despite a very short turn-around time. Using this assay, late-night salivary cortisol concentrations below 8.9 nmol/L are typically found in healthy volunteers.
测定深夜唾液皮质醇浓度越来越多地被用作疑似库欣综合征的筛查试验。深夜样本中的皮质醇浓度通常极低,并且已有不同检测方法的特异性参考范围的报道。因此,我们研究的目的是评估首个专门用于唾液检测的自动化皮质醇免疫分析方法性能,并建立该检测方法的深夜采样参考范围数据。
使用罗氏Cobas皮质醇检测法(罗氏诊断公司)测定唾液皮质醇。在包括两个试剂批次的双中心评估方案中,使用五个不同浓度范围的唾液混合样本评估该检测方法的批间不精密度。通过系列稀释测试线性。使用市售唾液采样装置(Salivette,赛多利斯公司)于23:00从100名表面健康的志愿者采集唾液样本。20个样本的子集用于与同位素稀释液相色谱 - 串联质谱法进行方法比较。
对于12.9至2.6 nmol/L的平均皮质醇浓度,批间变异系数(n = 20)在11.6%至40.4%之间,估计功能灵敏度约为5.0 nmol/L。该检测方法在1.0至8.3 nmol/L的最低浓度范围内也给出了线性结果。健康个体的深夜唾液皮质醇平均水平为5.0 nmol/L;绝对范围为1.4 - 16.7 nmol/L,第95百分位数为8.9 nmol/L。与免疫分析结果相比,同位素稀释液相色谱 - 串联质谱法测得的浓度显著更低(平均浓度分别为1.8和4.4 nmol/L)。
尽管周转时间非常短,但所研究的自动化检测方法在深夜唾液皮质醇所需的极低浓度范围内具有可接受的分析性能。使用该检测方法,健康志愿者的深夜唾液皮质醇浓度通常低于8.9 nmol/L。