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首页> 外文期刊>Hormone and Metabolic Research >Diagnosis of adrenal insufficiency using the GHRP-6 Test: comparison with the insulin tolerance test in patients with hypothalamic-pituitary-adrenal disease.
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Diagnosis of adrenal insufficiency using the GHRP-6 Test: comparison with the insulin tolerance test in patients with hypothalamic-pituitary-adrenal disease.

机译:使用GHRP-6测试诊断肾上腺功能不全:与下丘脑-垂体-肾上腺疾病患者的胰岛素耐受性测试进行比较。

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摘要

The insulin tolerance test (ITT) is considered the gold standard for the diagnosis of adrenal insufficiency (AI). However, the test is unpleasant to perform and has the risk of serious complications. We therefore evaluated the clinical applicability of GHRP6, which is a known activator of the hypothalamic-pituitary-adrenal (HPA) axis, to test for AI. For this purpose a comparative clinical study was designed. Forty-nine patients with suspected dysfunction of the HPA axis and 20 healthy controls were enrolled. The ITT was performed in patients, and GHRP6 (1 microg/kg) testing in patients and controls. Serum cortisol over 90 min after GHRP6, in comparison to the ITT, was the main outcome measure. Thirty-one patients had a peak cortisol response of less than 500 nmol/l during ITT and were considered adrenal insufficient. For GHRP6, the mean cortisol peak was 227+/-25.7 nmol/l in the AI group versus 395+/-35.3 nmol/l in the adrenal sufficient (AS) group. ROC analysis of peak cortisol levels during GHRP6 test suggested an optimal threshold of 299 nmol/l for the diagnosis of AI (Sens. 71.0%, Spec. 77.8%). Applying upper (416 nmol/l) and lower (137 nmol/l) thresholds with high specificities in combination with early morning cortisol established the diagnosis in nearly half of the patients, even when the GHRP6 test is limited to 30 min duration. GHRP6 led to significant activation of the HPA axis with no detectable side effects, but had limited accuracy in comparison to the ITT.
机译:胰岛素耐受性测试(ITT)被认为是诊断肾上腺功能不全(AI)的金标准。但是,该测试难以执行,并且有发生严重并发症的风险。因此,我们评估了下丘脑-垂体-肾上腺(HPA)轴的已知激活剂GHRP6在临床上的适用性,以测试AI。为此目的,设计了比较临床研究。入组49位怀疑HPA轴功能障碍的患者和20位健康对照。在患者中进行了ITT,并在患者和对照中进行了GHRP6(1 microg / kg)测试。与ITT相比,GHRP6后90分钟的血清皮质醇是主要的结局指标。在ITT期间有31名患者的皮质醇峰值应答小于500 nmol / l,被认为是肾上腺皮质激素不足。对于GHRP6,AI组平均皮质醇峰为227 +/- 25.7 nmol / l,而肾上腺皮质激素充足(AS)组为395 +/- 35.3 nmol / l。在GHRP6测试期间对峰值皮质醇水平的ROC分析表明,诊断AI的最佳阈值为299 nmol / l(灵敏度71.0%,规格77.8%)。即使GHRP6检测仅限于30分钟,将高特异性的较高(416 nmol / l)和较低(137 nmol / l)阈值与清晨皮质醇结合使用也可对近一半的患者进行诊断。 GHRP6导致HPA轴显着激活,没有可检测到的副作用,但与ITT相比,准确性有限。

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