Revised GH and cortisol cut-points for the glucagon stimulation test in the evaluation of GH and hypothalamic–pituitary–adrenal axes in adults: results from a prospective randomized multicenter study

Autor: Amir H. Hamrahian, James Bena, Murray B. Gordon, Beverly M. K. Biller, Karen J. Pulaski-Liebert, Kevin C.J. Yuen
Rok vydání: 2016
Předmět:
Blood Glucose
Male
Hydrocortisone
Endocrinology
Diabetes and Metabolism

Pituitary-Adrenal System
Craniopharyngioma
0302 clinical medicine
Endocrinology
Reference Values
Insulin
Medicine
Central Nervous System Cysts
Human Growth Hormone
Middle Aged
030220 oncology & carcinogenesis
Female
medicine.symptom
Adenoma
Adult
Hypothalamo-Hypophyseal System
medicine.medical_specialty
Side effect
medicine.drug_class
Nausea
030209 endocrinology & metabolism
Sensitivity and Specificity
Hypopituitarism
03 medical and health sciences
Internal medicine
Adrenal insufficiency
Humans
Hypoglycemic Agents
Pituitary Neoplasms
Dosing
Aged
Dose-Response Relationship
Drug

business.industry
Body Weight
Insulin tolerance test
Gold standard (test)
Glucagon
medicine.disease
Hormones
Estrogen
Case-Control Studies
Cosyntropin
business
Body mass index
Adrenal Insufficiency
Zdroj: Pituitary. 19:332-341
ISSN: 1573-7403
1386-341X
DOI: 10.1007/s11102-016-0712-7
Popis: Recent studies suggest using lower GH cut-points for the glucagon stimulation test (GST) in diagnosing adult GH deficiency (GHD), especially in obese patients. There are limited data on evaluating GH and hypothalamic–pituitary–adrenal (HPA) axes using weight-based dosing for the GST. To define GH and cortisol cut-points to diagnose adult GHD and secondary adrenal insufficiency (SAI) using the GST, and to compare fixed-dose (FD: 1 or 1.5 mg in patients >90 kg) with weight-based dosing (WB: 0.03 mg/kg). Response to the insulin tolerance test (ITT) was considered the gold standard, using GH and cortisol cut-points of ≥3 ng/ml and ≥18 µg/dL, respectively. 28 Patients with hypothalamic-pituitary disease and 1–2 (n = 14) or ≥3 (n = 14) pituitary hormone deficiencies, and 14 control subjects matched for age, sex, estrogen status and body mass index (BMI) underwent the ITT, FD- and WB-GST in random order. Age, sex ratio and BMI were comparable between the three groups. The best GH cut-point for diagnosis of GHD was 1.0 (92 % sensitivity, 100 % specificity) and 2.0 ng/mL (96 % sensitivity and 100 % specificity) for FD- and WB-GST, respectively. Age negatively correlated with peak GH during FD-GST (r = −0.32, P = 0.04), but not WB-GST. The best cortisol cut-point for diagnosis of SAI was 8.8 µg/dL (92 % sensitivity, 100 % specificity) and 11.2 µg/dL (92 % sensitivity and 100 % specificity) for FD-GST and WB-GST, respectively. Nausea was the most common side effect, and one patient had a seizure during the FD-GST. The GST correctly classified GHD using GH cut-points of 1 ng/ml for FD-GST and 2 ng/ml for WB-GST, hence using 3 ng/ml as the GH cut-point will misclassify some GH-sufficient adults. The GST may also be an acceptable alternative to the ITT for evaluating the HPA axis utilizing cortisol cut-points of 9 µg/dL for FD-GST and 11 µg/dL for WB-GST.
Databáze: OpenAIRE