Department of Endocrinology, Erciyes University Medical School, Kayseri, Turkey,
Department of Endocrinology, Erciyes University Medical School, Kayseri, Turkey.
Arch Endocrinol Metab. 2021 May 18;64(5):608-613. doi: 10.20945/2359-3997000000266.
To investigate whether a combination of the low-dose (1 μg) adrenocorticotropin (ACTH) stimulation test and glucagon stimulation test (GST) could overcome the problem of equivocal results with the GST or ACTH test alone in patients with pituitary disorders.
The study included 41 adult patients with pituitary disorders and 20 healthy subjects who underwent evaluation of cortisol response to ACTH, GST, and a combination of both tests. Blood samples for cortisol measurement were obtained at baseline and 30, 60, 90, and 120 minutes after intravenous administration of ACTH 1 μg and 90, 120, 150, 180, 210, and 240 minutes after subcutaneous injection of glucagon 1 mg. The combination test was performed by injecting ACTH 1 μg at the 180-minute time point of the GST, with blood samples for cortisol measurement obtained at 210 and 240 minutes.
Overall, 28 patients with normal cortisol response to both tests also had a normal cortisol response to the combination test. Ten patients with adrenal insufficiency in both tests also had adrenal insufficiency in the combination test, including a patient who had a peak cortisol value of 12.4 μg/dL (which is the cutoff value for the combination test). Two patients with adrenal insufficiency in the ACTH stimulation test and one patient with adrenal insufficiency in the GST had normal cortisol responses to the combination test.
By using an appropriate cutoff value, the combination test may offer additional information in patients with equivocal results in the GST and ACTH stimulation test.
研究低剂量(1μg)促肾上腺皮质激素(ACTH)刺激试验和胰高血糖素刺激试验(GST)联合应用是否可以克服 GST 或 ACTH 试验单独应用时结果不确定的问题。
本研究纳入了 41 例垂体疾病患者和 20 例健康对照者,他们接受了 ACTH、GST 及二者联合试验评估皮质醇反应。在静脉注射 1μg ACTH 后,分别于 0、30、60、90 和 120 分钟,以及皮下注射 1mg 胰高血糖素后 90、120、150、180、210 和 240 分钟,采集血样测定皮质醇。在 GST 的 180 分钟时联合应用 ACTH 1μg,于 210 和 240 分钟时采集血样测定皮质醇,进行联合试验。
总的来说,28 例对两种试验均有正常皮质醇反应的患者也对联合试验有正常的皮质醇反应。10 例在两种试验中均有肾上腺功能不全的患者也在联合试验中存在肾上腺功能不全,包括 1 例患者的皮质醇峰值为 12.4μg/dL(这是联合试验的截止值)。2 例在 ACTH 刺激试验中存在肾上腺功能不全和 1 例在 GST 中存在肾上腺功能不全的患者对联合试验有正常的皮质醇反应。
通过使用适当的截止值,联合试验可以为 GST 和 ACTH 刺激试验结果不确定的患者提供额外的信息。