Low-Dose and Standard Overnight and Low Dose-Two Day Dexamethasone Suppression Tests in Patients with Mild and/or Episodic Hypercortisolism

Autor: Mastaneh Haykani, Jennifer L. A. Tran, Jason Saidian, Theodore C. Friedman, Hraya K. Shahinian, Ian E. McCutcheon, Michael Mangubat, Mohan Zopey, Antolice Thomas, Martin Lee, Rahul Nachnani, Nesyah Shaesteh, Mona Mojtahedzadeh
Rok vydání: 2018
Předmět:
Male
Hydrocortisone
Endocrinology
Diabetes and Metabolism

Clinical Biochemistry
Cushing's syndrome
030204 cardiovascular system & hematology
Biochemistry
Dexamethasone
0302 clinical medicine
Endocrinology
polycyclic compounds
Cushing Syndrome
Morning
Pediatric
Low dose
periodic
General Medicine
Middle Aged
6.1 Pharmaceuticals
Dexamethasone suppression test
Female
episodic
Drug
hormones
hormone substitutes
and hormone antagonists

medicine.drug
Adult
endocrine system
medicine.medical_specialty
Cortisol awakening response
Adolescent
Clinical Trials and Supportive Activities
Clinical Sciences
030209 endocrinology & metabolism
cortisol
Article
Dose-Response Relationship
Young Adult
Endocrinology & Metabolism
03 medical and health sciences
Rare Diseases
Clinical Research
Internal medicine
medicine
Humans
In patient
Dose-Response Relationship
Drug

hypercortisolism
business.industry
Biochemistry (medical)
Evaluation of treatments and therapeutic interventions
Dexamethasone suppression
business
Serum cortisol
Zdroj: Hormone and metabolic research = Hormon-und Stoffwechselforschung = Hormones et metabolisme, vol 50, iss 6
ISSN: 1439-4286
0018-5043
DOI: 10.1055/a-0603-3868
Popis: We previously reported on the lack of utility of the 1 mg overnight dexamethasone (DEX) test in mild and/or periodic Cushing’s syndrome, as most patients with the condition suppressed to 1 mg DEX. It is possible that a lower dose of DEX as part of an overnight DEX test might be able to distinguish between mild and/or periodic Cushing’s syndrome and those without the condition. The objective of the current study is to determine the sensitivity and specificity of a 0.25 mg overnight DEX suppression test, the standard 1 mg overnight DEX suppression test, and the two-day low-dose (Liddle test) DEX suppression test with and without correction for DEX levels in patients evaluated for mild and/or periodic Cushing’s syndrome. Thirty patients determined to have Cushing’s syndrome by biochemical testing and 14 patients determined not to have the condition had the 0.25 mg and standard 1 mg overnight DEX suppression test and the two-day low-dose DEX suppression tests. Our results show that morning serum cortisol and cortisol/DEX ratios following an overnight dexamethasone suppression test were similar in patients with Cushing’s syndrome and those not having Cushing’s syndrome. However, a morning cortisol value above 7.6 μg/dl following a dose of DEX of 0.25 mg was found in 12 patients with Cushing’s syndrome and none in those not having Cushing’s syndrome, suggesting that a high cortisol value after this low dose of dexamethasone can indicate that further testing for Cushing’s syndrome is warranted. Our data suggest that the traditional 1 mg overnight or the 2 mg/2 day DEX suppression testing should no longer be used as a screening test in patients who could have mild and/or periodic Cushing’s syndrome, while the 0.25 mg dose of DEX may pick up some patients with mild Cushing’s syndrome.
Databáze: OpenAIRE