Tan Sarah Ying Tse, Tan Hong Chang, Zhu Ling, Loh Lih Ming, Lim Dawn Shao Ting, Swee Du Soon, Chan Yoke Ling, Lim Huee Boon, Ling Shiau Lee, Ou En Jun, Teo Wynn Ee, Zhang Xiao Ping, Goh Hui Fen, Kek Peng Chin
Department of Endocrinology, Singapore General Hospital, Singapore.
Department of Speciality Nursing, Singapore General Hospital, Singapore.
Endocr Connect. 2023 Mar 28;12(4). doi: 10.1530/EC-23-0004. Print 2023 Apr 1.
Adrenal insufficiency (AI) is potentially life-threatening, and accurate diagnosis is crucial. The first-line diagnostic test, the adrenocorticotrophic hormone (ACTH) stimulation test, measures serum total cortisol. However, this is affected in states of altered albumin or cortisol-binding globulin levels, limiting reliability. Salivary cortisol reflects free bioactive cortisol levels and is a promising alternative. However, few studies are available, and heterogenous methodologies limit applicability.
This study prospectively recruited 42 outpatients undergoing evaluation for AI, excluding participants with altered cortisol-binding states. Serum (immunoassay) and salivary (liquid chromatography tandem mass spectrometry) cortisol levels were sampled at baseline, 30 min, and 60 min following 250 µg synacthen administration. AI was defined as a peak serum cortisol level <500 nmol/L in accordance with guidelines.
The study recruited 21 (50%) participants with AI and 21 without AI. There were no significant differences in baseline characteristics, blood pressure, or sodium levels between groups. Following synacthen stimulation, serum and salivary cortisol levels showed good correlation at all timepoints (R2 = 0.74, P < 0.001), at peak levels (R2 = 0.72, P < 0.001), and at 60 min (R2 = 0.72, P < 0.001). A salivary cortisol cut-off of 16.0 nmol/L had a sensitivity of 90.5% and a specificity of 76.2% for the diagnosis of AI.
This study demonstrates a good correlation between serum and salivary cortisol levels during the 250 µg synacthen test. A peak salivary cortisol cut-off of 16.0 nmol/L can be used for the diagnosis of AI. It is a less invasive alternative to evaluate patients with suspected AI. Its potential utility in the diagnosis of AI in patients with altered cortisol-binding states should be further studied.
肾上腺功能不全(AI)可能危及生命,准确诊断至关重要。一线诊断测试,即促肾上腺皮质激素(ACTH)刺激试验,测量血清总皮质醇。然而,这在白蛋白或皮质醇结合球蛋白水平改变的状态下会受到影响,限制了可靠性。唾液皮质醇反映游离生物活性皮质醇水平,是一种有前景的替代方法。然而,相关研究较少,且方法各异限制了其适用性。
本研究前瞻性招募了42名接受AI评估的门诊患者,排除皮质醇结合状态改变的参与者。在给予250μg 合成促肾上腺皮质激素后,于基线、30分钟和60分钟采集血清(免疫测定)和唾液(液相色谱串联质谱法)皮质醇水平样本。根据指南,AI定义为血清皮质醇峰值水平<500nmol/L。
该研究招募了21名(50%)AI患者和21名非AI患者。两组之间在基线特征、血压或钠水平方面无显著差异。在合成促肾上腺皮质激素刺激后,血清和唾液皮质醇水平在所有时间点(R2 = 0.74,P < 0.001)、峰值水平(R2 = 0.72,P < 0.001)和60分钟时(R2 = 0.72,P < 0.001)均显示出良好的相关性。唾液皮质醇截断值为16.0nmol/L时,诊断AI的敏感性为90.5%,特异性为76.2%。
本研究证明了在250μg合成促肾上腺皮质激素试验期间血清和唾液皮质醇水平之间具有良好的相关性。唾液皮质醇峰值截断值为16.0nmol/L可用于AI的诊断。它是评估疑似AI患者的一种侵入性较小的替代方法。其在皮质醇结合状态改变的患者中诊断AI的潜在效用应进一步研究。