Mayenknecht J, Diederich S, Bähr V, Plöckinger U, Oelkers W
Department of Medicine, Klinikum Benjamin Franklin, Freie Universität Berlin, Germany.
J Clin Endocrinol Metab. 1998 May;83(5):1558-62. doi: 10.1210/jcem.83.5.4831.
Tetracosactin [corticotropin-(1-24)] is used for clinical testing of adrenocortical responsiveness. The usual dose [high dose test (HDT)] is 250 micrograms. With this test, patients with mild secondary adrenal insufficiency are usually not identified, thus putting them at risk of an adrenal crisis in stressful situations. It was recently reported that a tetracosactin test with approximately 1 micrograms [low dose test (LDT)] identifies patients with mild forms of pituitary-adrenal insufficiency. We performed both the HDT and the LDT in 35 control subjects and in 44 patients with pituitary disease, mostly pituitary tumors. In these patients, more sensitive reference tests for evaluating the pituitary-adrenal axis (insulin-induced hypoglycemia, metyrapone, and CRH tests) were also performed. In the HDT, plasma cortisol was measured 30 and 60 min after tetracosactin injection; in the LDT (0.5 microgram/m2 body surface area), plasma cortisol was measured 20, 30, 40, 50, and 60 min postinjection. In 6 control subjects, tetracosactin plasma levels were also measured after injection. In the HDT, the correlation between 30 and 60 min cortisol levels was extremely high (r = 0.991; P < 0.0001), but the correlation of the LDT with the HDT at 30 min was also highly significant (r = 0.948; P < 0.0001). The lower normal limit of cortisol responses (means of controls minus 2 SD) at 30 min was lower in the LDT by 3.1 micrograms/dL (85 nmol/L) than in the HDT. Compared with the reference tests, the diagnostic sensitivities of the HDT and the LDT were almost identical. Both tests identified patients with moderately to severely pathological insulin and metyrapone tests, but not those with slightly pathological reference tests. In the HDT, plasma tetracosactin rose to more than 60,000 pg/mL shortly after injection. In the LDT, it rose to 1,900 pg/mL. Both concentrations stimulate cortisol (supra-) maximally. Together, these data show that in pituitary disorders the results of the LDT and the HDT are almost identical. Plasma tetracosactin levels in the LDT still rise to levels that maximally stimulate the adrenal. Tetracosactin testing with low or high doses cannot generally replace the more expensive and cumbersome insulin or metyrapone tests.
二十四肽促皮质素[促肾上腺皮质激素-(1 - 24)]用于肾上腺皮质反应性的临床检测。常用剂量[高剂量试验(HDT)]为250微克。通过这项试验,轻度继发性肾上腺皮质功能不全的患者通常无法被识别出来,因此他们在应激情况下有发生肾上腺危象的风险。最近有报道称,使用约1微克的二十四肽促皮质素试验[低剂量试验(LDT)]可识别出轻度垂体 - 肾上腺功能不全的患者。我们对35名对照受试者和44名患有垂体疾病(主要是垂体肿瘤)的患者进行了HDT和LDT。在这些患者中,还进行了用于评估垂体 - 肾上腺轴的更敏感的参考试验(胰岛素诱发低血糖试验、甲吡酮试验和促肾上腺皮质激素释放激素试验)。在HDT中,注射二十四肽促皮质素后30分钟和60分钟测量血浆皮质醇;在LDT(0.5微克/平方米体表面积)中,注射后20、30、40、50和60分钟测量血浆皮质醇。在6名对照受试者中,注射后也测量了二十四肽促皮质素的血浆水平。在HDT中,30分钟和60分钟皮质醇水平之间的相关性极高(r = 0.991;P < 0.0001),但LDT与HDT在30分钟时的相关性也非常显著(r = 0.948;P < 0.0001)。LDT在30分钟时皮质醇反应的正常下限(对照组均值减去2个标准差)比HDT低3.1微克/分升(85纳摩尔/升)。与参考试验相比,HDT和LDT的诊断敏感性几乎相同。两项试验都能识别出胰岛素试验和甲吡酮试验中度至重度异常的患者,但不能识别出参考试验轻度异常的患者。在HDT中,注射后不久血浆二十四肽促皮质素升至超过60,000皮克/毫升。在LDT中,它升至1,900皮克/毫升。两种浓度都能最大程度地刺激皮质醇分泌。总之,这些数据表明,在垂体疾病中,LDT和HDT的结果几乎相同。LDT中血浆二十四肽促皮质素水平仍升至能最大程度刺激肾上腺的水平。低剂量或高剂量的二十四肽促皮质素试验通常不能替代更昂贵且繁琐的胰岛素试验或甲吡酮试验。