Diagnostic Accuracy Study of Morning Salivary Cortisone for Screening Adrenal Insufficiency in a Real-World Cohort.

IF 5.1
Constantinos Televantos, Phillip J Monaghan, Maria Michaelidou, Lillian Ruiheng Chen, Mohammed Ahmed, Jan Hoong Ho, Shaishav Dhage, Claire Higham, Brian Keevil, Safwaan Adam
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Abstract

Context: Morning serum cortisol is used to screen for adrenal insufficiency, but requires venepuncture, early morning clinic attendance, and may be affected by altered corticosteroid-binding globulin (CBG) levels. Salivary cortisone is a non-invasive, home-based alternative.

Objective: To assess the diagnostic accuracy of morning salivary cortisone for screening adrenal insufficiency and establish clinically relevant thresholds.

Design: Retrospective cross-sectional diagnostic accuracy study (2017 to 2024).

Setting: Single tertiary oncology and endocrinology center in the United Kingdom.

Participants: Consecutive patients undergoing adrenocorticotropin hormone (ACTH) stimulation test for suspected adrenal insufficiency.

Intervention: Salivary sampling for cortisone and cortisol.

Main outcome measures: Sensitivity and specificity of baseline salivary cortisone.

Results: A total of 517 ACTH stimulation tests in 449 participants were included; adrenal insufficiency was confirmed in 104 tests (20.1%). Baseline salivary cortisone accurately predicted adrenal insufficiency (area under the receiver operating characteristic curve [AUC] 0.93, 95% CI [0.91-0.95]), similar to serum cortisol (0.93, 0.90-0.95; p = 0.67) and superior to salivary cortisol (0.87, 0.82-0.91; p = 0.00063). A baseline salivary cortisone rule-out threshold ≥703 ng/dL (19.5 nmol/L) (sensitivity 0.97 [95% CI 0.92-0.99]; specificity 0.59 [0.54-0.63]) and a rule-in threshold <180 ng/dL (5.0 nmol/L) (sensitivity 0.58 [0.48-0.67]; specificity 0.97 [0.95-0.98]) provided the highest net benefit. An intermediate threshold <389 ng/dL (10.8 nmol/L) (sensitivity 0.83 [0.74-0.89]; specificity 0.87 [0.83-0.90]) identified patients for whom glucocorticoid cover should be considered while awaiting confirmatory testing.

Conclusion: Baseline morning salivary cortisone performs at least as well as serum cortisol for adrenal insufficiency screening.

早晨唾液可的松在真实世界队列中筛查肾上腺功能不全的诊断准确性研究。
背景:清晨血清皮质醇用于筛查肾上腺功能不全,但需要静脉穿刺、清晨门诊就诊,并可能受到皮质类固醇结合球蛋白(CBG)水平改变的影响。唾液可的松是一种无创的家庭替代疗法。目的:评价晨吐可的松对肾上腺功能不全的诊断准确性,建立临床相关阈值。设计:回顾性横断面诊断准确性研究(2017 - 2024)。地点:英国单一三级肿瘤和内分泌中心。参与者:连续接受促肾上腺皮质激素(ACTH)刺激试验的疑似肾上腺功能不全患者。干预:唾液取样检测可的松和皮质醇。主要观察指标:基线唾液可的松的敏感性和特异性。结果:共纳入449例受试者517次ACTH刺激试验;104例(20.1%)证实肾上腺功能不全。基线唾液可的松准确预测肾上腺功能不全(受试者工作特征曲线下面积[AUC] 0.93, 95% CI[0.91-0.95]),与血清皮质醇相似(0.93,0.90-0.95,p = 0.67),优于唾液皮质醇(0.87,0.82-0.91,p = 0.00063)。基线唾液可的松排除阈值≥703 ng/dL (19.5 nmol/L)(敏感性0.97 [95% CI 0.92-0.99];特异性0.59[0.54-0.63])和规则阈值结论:基线唾液可的松在肾上腺功能不全筛查中的作用至少与血清皮质醇一样好。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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