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Unique Identifier
98169802
Authors
al-Saadi N. Diederich S. Oelkers W.
Institution
Department of Internal Medicine, Klinikum
Benjamin Franklin (Steglitz), Freie Universitat Berlin, Germany.
Title
A very high dose dexamethasone suppression
test for differential diagnosis of Cushing's syndrome.
Source
Clinical Endocrinology. 48(1):45-51, 1998
Jan.
MeSH Subject Headings
Adenoma/bl [Blood]
Adenoma/co [Complications]
Adenoma/ur [Urine]
Adrenal Gland Neoplasms/bl [Blood]
Adrenal Gland Neoplasms/co [Complications]
Adrenal Gland Neoplasms/ur [Urine]
Adult
ACTH Syndrome, Ectopic/bl [Blood]
ACTH Syndrome, Ectopic/co [Complications]
ACTH Syndrome, Ectopic/ur [Urine]
Corticotropin/bl [Blood]
*Corticotropin-Releasing Hormone/du
[Diagnostic Use]
Cushing Syndrome/bl [Blood]
*Cushing Syndrome/di [Diagnosis]
Cushing Syndrome/ur [Urine]
Depression, Chemical
Dexamethasone/ad [Administration &
Dosage]
*Dexamethasone/du [Diagnostic Use]
Diagnosis, Differential
Drug Administration Schedule
Female
Glucocorticoids, Synthetic/ad
[Administration & Dosage]
*Glucocorticoids, Synthetic/du [Diagnostic
Use]
Human
*Hydrocortisone/bl [Blood]
Hydrocortisone/ur [Urine]
Male
Middle Age
Pituitary Neoplasms/bl [Blood]
Pituitary Neoplasms/co [Complications]
Pituitary Neoplasms/ur [Urine]
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 8mg 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.
Registry Numbers
0 (Glucocorticoids, Synthetic). 50-02-2
(Dexamethasone). 50-23-7
(Hydrocortisone). 9002-60-2
(Corticotropin). 9015-71-8
(Corticotropin-Releasing Hormone).