Department of Endocrinology, Diabetes and Metabolism, University Duisburg-Essen, Essen, Germany.
Department of Clinical Chemistry, University Duisburg-Essen, Essen, Germany.
Horm Metab Res. 2021 Oct;53(10):662-671. doi: 10.1055/a-1608-1720. Epub 2021 Oct 4.
Due to high morbidity and mortality of untreated hypercortisolism, a prompt diagnosis is essential. Measurement of late-night salivary cortisol provides a simple and non-invasive method. However, thresholds and reference ranges differ among studies. The goal of this study was to define a threshold of late-night salivary cortisol for the diagnosis of hypercortisolism based on the used assay. Moreover, the influence of different aetiologies of hypercortisolism and individual comorbidities were investigated. Prospective analyses of 217 patients, including 36 patients with proven hypercortisolism were carried out. A sum of 149 patients with suspicion of hypercortisolism but negative endocrine testing and 32 patients with hypercortisolism in remission served as control group. Late-night salivary cortisol was measured using an automated chemiluminescence immunoassay. Cut-off values were calculated by ROC analysis. The calculated cut-off value for the diagnosis of hypercortisolism was 10.1 nmol/l (sensitivity 94%; specificity 84%). Only slightly lower thresholds were obtained in patients with suspected hypercortisolism due to weight gain/obesity (9.1 nmol/l), hypertension or adrenal tumours (both 9.8 nmol/l) or pituitary adenomas (9.5 nmol/l). The late-night salivary cortisol threshold to distinguish between Cushing's disease and Cushing's disease in remission was 9.2 nmol/l. The cut-off value for the diagnosis of ectopic ACTH-production was 109.0 nmol/l (sensitivity 50%, specificity 92%). Late-night salivary cortisol is a convenient and reliable parameter for the diagnosis of hypercortisolism. Except for ectopic ACTH-production, thresholds considering different indications for evaluation of hypercortisolism were only slightly different. Therefore, they might only be useful if late-night salivary cortisol results near the established cut-off value are present.
由于未经治疗的皮质醇增多症的发病率和死亡率很高,因此及时诊断至关重要。测量深夜唾液皮质醇提供了一种简单且非侵入性的方法。然而,不同研究的阈值和参考范围不同。本研究的目的是基于所用检测方法,确定用于诊断皮质醇增多症的深夜唾液皮质醇阈值。此外,还研究了不同病因皮质醇增多症和个体合并症的影响。对 217 例患者进行了前瞻性分析,其中包括 36 例确诊的皮质醇增多症患者。 149 例疑似皮质醇增多症但内分泌检查阴性的患者和 32 例皮质醇增多症缓解的患者作为对照组。使用自动化化学发光免疫分析测量深夜唾液皮质醇。通过 ROC 分析计算截止值。诊断皮质醇增多症的计算截止值为 10.1 nmol/l(敏感性 94%;特异性 84%)。由于体重增加/肥胖(9.1 nmol/l)、高血压或肾上腺肿瘤(均为 9.8 nmol/l)或垂体腺瘤(9.5 nmol/l)而疑似皮质醇增多症的患者中,获得的阈值略低。区分库欣病和库欣病缓解的深夜唾液皮质醇阈值为 9.2 nmol/l。异位 ACTH 产生的诊断截止值为 109.0 nmol/l(敏感性 50%,特异性 92%)。深夜唾液皮质醇是诊断皮质醇增多症的一种方便可靠的参数。除了异位 ACTH 产生外,考虑不同皮质醇增多症评估指征的阈值仅略有不同。因此,只有在深夜唾液皮质醇结果接近既定截止值时,它们才可能有用。