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用于库欣综合征鉴别诊断的大剂量地塞米松抑制试验。

A very high dose dexamethasone suppression test for differential diagnosis of Cushing's syndrome.

作者信息

al-Saadi N, Diederich S, Oelkers W

机构信息

Department of Internal Medicine, Klinikum Benjamin Franklin (Steglitz), Freie Universität Berlin, Germany.

出版信息

Clin Endocrinol (Oxf). 1998 Jan;48(1):45-51. doi: 10.1046/j.1365-2265.1998.00345.x.

Abstract

OBJECTIVE

The high-dose dexamethasone (dex) suppression test of cortisol secretion (8 x 2 mg dex over two days or 8 mg overnight) is a mainstay in the differential diagnosis of Cushing's syndrome (CS). In some patients with pituitary Cushing's disease (CD), however, plasma cortisol is not suppressed to < 50% of control by 8 mg of dex. We therefore hypothesized that a higher dose of dex might produce more effective suppression of cortisol secretion in CD.

DESIGN AND SUBJECTS

We routinely tested the diagnostic efficacy of a very high dose of dex (32 mg, i.e. 4 x 8 mg in 24 hours) in comparison with the 8 mg overnight dex test in a population of patients with CD, in which an unusually high percentage was refractory to 8 mg dex. End points were the suppression of plasma cortisol, plasma ACTH and urinary free cortisol (UFC) to < 50% of control. Corticotrophin releasing hormone (human CRH) tests were also performed.

RESULTS

Eleven out of 26 (11/26) patients with CD (42%), among them six with pituitary macro-adenomas, failed to show suppression of plasma cortisol after 8 mg dex. Five out of 19 patients (26%) with CD failed to suppress after 32 mg dex. Only 3/19 (16%) failed to suppress UFC after 32 mg dex. In nonpituitary CS (n = 11), only one patient with macro-nodular adrenal hyperplasia showed significant suppression of plasma cortisol, but not UFC, after 32 mg dex. ACTH suppression after 8 or 32 mg dex was often less pronounced than that of cortisol and was of no diagnostic value. Cortisol stimulation by > or = 23% after hCRH injection differentiated 100% of patients with CD from other forms of CS.

CONCLUSION

In this series, the hCRH test was the most reliable test for the differential diagnosis of Cushing's syndrome. The 32 mg dexamethasone test with measurement of urinary free cortisol was clearly superior to the 8 mg test and to other aspects of the very high dose dexamethasone test. It can be recommended for 'non-suppressible' patients with ACTH-dependent Cushing's syndrome and can be performed on outpatients.

摘要

目的

皮质醇分泌的高剂量地塞米松(dex)抑制试验(两天内8次给予2mg地塞米松或夜间给予8mg)是库欣综合征(CS)鉴别诊断的主要手段。然而,在一些垂体性库欣病(CD)患者中,8mg地塞米松未能使血浆皮质醇抑制至对照值的<50%。因此,我们推测更高剂量的地塞米松可能对CD患者的皮质醇分泌产生更有效的抑制作用。

设计与研究对象

我们常规测试了非常高剂量地塞米松(32mg,即24小时内4次给予8mg)与夜间8mg地塞米松试验相比,在一群CD患者中的诊断效果,这些患者中对8mg地塞米松无反应的比例异常高。观察终点为血浆皮质醇、血浆促肾上腺皮质激素(ACTH)和尿游离皮质醇(UFC)抑制至对照值的<50%。还进行了促肾上腺皮质激素释放激素(人CRH)试验。

结果

26例CD患者中有11例(11/26,42%),其中6例患有垂体大腺瘤,在给予8mg地塞米松后血浆皮质醇未出现抑制。19例CD患者中有5例(26%)在给予32mg地塞米松后未出现抑制。19例中只有3例(16%)在给予32mg地塞米松后UFC未被抑制。在非垂体性CS患者(n = 11)中,只有1例大结节性肾上腺增生患者在给予32mg地塞米松后血浆皮质醇有显著抑制,但UFC未被抑制。给予8mg或32mg地塞米松后ACTH的抑制通常不如皮质醇明显,且无诊断价值。注射hCRH后皮质醇刺激增加≥23%可将100%的CD患者与其他形式的CS区分开来。

结论

在本研究系列中,hCRH试验是库欣综合征鉴别诊断中最可靠的试验。测量尿游离皮质醇的32mg地塞米松试验明显优于8mg试验以及非常高剂量地塞米松试验的其他方面。对于依赖ACTH的“不可抑制”的库欣综合征患者可推荐使用,且可在门诊进行。

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