Evaluation of plasma ACTH in the metyrapone test is insufficient for the diagnosis of secondary adrenal insufficiency

Objective To determine whether a single measurement of ACTH instead of less available in daily practice 11-deoxycortisol assay is sufficient to rule out or confirm secondary adrenal insufficiency (SAI) in the short Metyrapone test. Design A retrospective analysis of diagnostic tests (Metyrapone and Synacthen tests) performed at our Center between 2016 and 2018 in patients with suspicion of secondary adrenal insufficiency. Material and methods In 103 patients short metyrapone test was performed with assessment of 11-deoxycortisol and ACTH concentration after Metyrapone administered at midnight. In 89 of them short Synacthen (SST) test was also done (1 or/and 250 mcg 1-24ACTH). ROC curves have been performed to evaluate the diagnostic performance of ACTH level in metyrapone test as the predictor of secondary adrenal insufficiency (SAI) analysing sensitivity and specificity for various possible thresholds proposed in literature. Results 40 (39%) of examined subjects were diagnosed as SAI, basing on post-Metyrapone 11-deoxycortisol concentration below 70 μg/l. In this group ACTH concentration was 128.1 ng/l (95% CI 96.8-159.4) versus 289.9 ng/l (95% CI 249.1-330.9) in patients with proper adrenal response. There was only a moderate positive correlation between ACTH and 11-deoxycortisol concentrations (r=0.5; p<0.05). The best cut off value of ACTH in relation to 11-deoxycortisol serum concentrations was 147 ng/l - with sensitivity of 73.2% and specificity 83.9%. However, plasma ACTH was>200ng/ml (the highest threshold proposed in literature) in 8 cases (20%) with positive diagnosis of SAI made on the basis of low 11-deoxycortisole and confirmed in short Synacthen test. Conclusion Our results indicate that for a valuable evaluation of the results of the metyrapone test, the more readily available plasma ACTH assay cannot replace the measurement of 11-deoxycortisol concentrations.

[1]  F. Keleştimur,et al.  Investigation of the Hypothalamo-pituitary-adrenal (HPA) axis: a contemporary synthesis , 2021, Reviews in Endocrine and Metabolic Disorders.

[2]  M. Coupaye,et al.  Central Adrenal Insufficiency Is Rare in Adults With Prader–Willi Syndrome , 2020, The Journal of clinical endocrinology and metabolism.

[3]  F. Ceccato,et al.  Central adrenal insufficiency: open issues regarding diagnosis and glucocorticoid treatment , 2018, Clinical chemistry and laboratory medicine.

[4]  G. Evatt,et al.  EST-SSRs as a resource for population genetic analyses , 2007, Heredity.

[5]  P. Dahlqvist,et al.  Clues for early detection of autoimmune Addison's disease – myths and realities , 2018, Journal of internal medicine.

[6]  Amir-Hossein Rahvar,et al.  Increased Cardiovascular Risk in Patients with Adrenal Insufficiency: A Short Review , 2017, BioMed research international.

[7]  B. Müller,et al.  Acute-Onset Panhypopituitarism Nearly Missed by Initial Cosyntropin Testing , 2017, Case Reports in Critical Care.

[8]  P. Schuetz,et al.  DIAGNOSTIC ACCURACY OF BASAL CORTISOL LEVEL TO PREDICT ADRENAL INSUFFICIENCY IN COSYNTROPIN TESTING: RESULTS FROM AN OBSERVATIONAL COHORT STUDY WITH 804 PATIENTS. , 2017, Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists.

[9]  R. Weiss,et al.  Endocrine Testing Protocols: Hypothalamic Pituitary Adrenal Axis , 2014 .

[10]  G. Johannsson,et al.  Cardiovascular and metabolic impact of glucocorticoid replacement therapy. , 2014, Frontiers of hormone research.

[11]  H. Raff,et al.  Physiological basis for the etiology, diagnosis, and treatment of adrenal disorders: Cushing's syndrome, adrenal insufficiency, and congenital adrenal hyperplasia. , 2014, Comprehensive Physiology.

[12]  P. Stewart,et al.  Central hypoadrenalism. , 2014, The Journal of clinical endocrinology and metabolism.

[13]  M. Rabijewski,et al.  Delay in Diagnosis of Adrenal Insufficiency Is a Frequent Cause of Adrenal Crisis , 2013, International journal of endocrinology.

[14]  M. Buchfelder,et al.  The rational use of pituitary stimulation tests. , 2010, Deutsches Arzteblatt international.

[15]  S. Hahner,et al.  Delayed Diagnosis of Adrenal Insufficiency Is Common: A Cross-Sectional Study in 216 Patients , 2010, The American journal of the medical sciences.

[16]  L. Nieman,et al.  Adrenal insufficiency: etiology, diagnosis and treatment , 2010, Current opinion in endocrinology, diabetes, and obesity.

[17]  M. Fassnacht,et al.  Impaired subjective health status in 256 patients with adrenal insufficiency on standard therapy based on cross-sectional analysis. , 2007, The Journal of clinical endocrinology and metabolism.

[18]  G. Johannsson,et al.  Premature mortality in patients with Addison's disease: a population-based study. , 2006, The Journal of clinical endocrinology and metabolism.

[19]  M. Andrioli,et al.  Isolated corticotrophin deficiency , 2006, Pituitary.

[20]  E. Fliers,et al.  Establishment of reference values for endocrine tests. Part IV: Adrenal insufficiency. , 2005, The Netherlands journal of medicine.

[21]  M. Maghnie,et al.  Evaluation of adrenal function in patients with growth hormone deficiency and hypothalamic-pituitary disorders: comparison between insulin-induced hypoglycemia, low-dose ACTH, standard ACTH and CRH stimulation tests. , 2005, European journal of endocrinology.

[22]  I. Silva,et al.  Early adrenocortical recovery after glucocorticoid therapy in children with leukemia. , 2004, The Journal of clinical endocrinology and metabolism.

[23]  K. Mann,et al.  Diagnosis of adrenal insufficiency: Evaluation of the corticotropin-releasing hormone test and Basal serum cortisol in comparison to the insulin tolerance test in patients with hypothalamic-pituitary-adrenal disease. , 2003, The Journal of clinical endocrinology and metabolism.

[24]  B. Allolio,et al.  Adrenal insufficiency , 2003, The Lancet.

[25]  L. Nieman Dynamic evaluation of adrenal hypofunction. , 2003, Journal of endocrinological investigation.

[26]  O. Jolobe,et al.  The low dose ACTH stimulation test is less sensitive than the overnight metyrapone test for the diagnosis of secondary hypoadrenalism. , 2000, Clinical endocrinology.

[27]  R. Carey,et al.  Adrenal insufficiency. , 1997, Current therapy in endocrinology and metabolism.

[28]  D. Streeten,et al.  The potential for serious consequences from misinterpreting normal responses to the rapid adrenocorticotropin test. , 1996, Journal of Clinical Endocrinology and Metabolism.

[29]  N. Stern,et al.  The role of the low dose (1 microgram) adrenocorticotropin test in the evaluation of patients with pituitary diseases. , 1995, The Journal of clinical endocrinology and metabolism.

[30]  V. Bähr,et al.  Pituitary function tests: comparison of ACTH and 11-deoxy-cortisol responses in the metyrapone test and with the insulin hypoglycemia test. , 2009, Experimental and clinical endocrinology.

[31]  T. Mckenna,et al.  The overnight single‐dose metyrapone test is a simple and reliable index of the hypothalamic‐pituitary‐adrenal axis , 1994, Clinical endocrinology.

[32]  S. Leeder,et al.  A population based study , 1993, The Medical journal of Australia.

[33]  J. Nicoloff,et al.  Screening for adrenocortical insufficiency with cosyntropin (synthetic ACTH). , 1971, Archives of Internal Medicine.