TY - JOUR
T1 - Low DHEAS
T2 - A sensitive and specific test for the detection of subclinical hypercortisolism in adrenal incidentalomas
AU - Dennedy, M. Conall
AU - Annamalai, Anand K.
AU - Prankerd-Smith, Olivia
AU - Freeman, Natalie
AU - Vengopal, Kuhan
AU - Graggaber, Johann
AU - Koulouri, Olympia
AU - Powlson, Andrew S.
AU - Shaw, Ashley
AU - Halsall, David J.
AU - Gurnell, Mark
N1 - Publisher Copyright:
Copyright © 2017 by the Endocrine Society.
PY - 2017/3/1
Y1 - 2017/3/1
N2 - Context: Subclinical hypercortisolism (SH) occurs in 5% to 30% of adrenal incidentalomas (AIs). Common screening tests for adrenocorticotropin-independent hypercortisolism have substantial false-positive rates, mandating further time and resource-intensive investigations. Objective: To determine whether low basal dehydroepiandrosterone sulfate (DHEAS) is a sensitive and specific screening test for SH in AI. Setting and Patients: In total, 185 patients with AI were screened for adrenal medullary (plasma metanephrines) and cortical [1 mg overnight dexamethasone suppression test (ONDST), 24-hour urinary free cortisol (UFC), serum DHEAS, plasma renin, and aldosterone] hyperfunction. Positive ONDST [1.8 mcg/dL (50 nmol/L)] and/or UFC (more than the upper limit of reference range) results were further investigated. We diagnosed SH when at least 2 of the following were met: raised UFC, raised midnight serum cortisol, 48-hour dexamethasone suppression test (DST) cortisol 1.8 mcg/dL (50 nmol/L). Results: 29 patients (16%)werediagnosedwith SH.Adrenocorticotropinwas,10 pg/mL (,2.2 pmol/L) in all patients with SH. We calculated age-and sex-specific DHEAS ratios (derived by dividing the DHEAS by the lower limit of the respective reference range) for all patients. Receiver operating characteristic curve analyses demonstrated that a ratio of 1.12 was sensitive (.99%) and specific (91.9%) for the diagnosis of SH. Cortisol following 1 mg ONDST of 1.9 mcg/dL (53 nmol/L) was a sensitive (.99%) screening test for SH but had lower specificity (82.9%). The 24-hour UFC lacked sensitivity (69%) and specificity (72%). Conclusion: A single basal measurement of DHEAS offers comparable sensitivity and greater specificity to the existing gold-standard 1mg DST for the detection of SH in patients with AIs.
AB - Context: Subclinical hypercortisolism (SH) occurs in 5% to 30% of adrenal incidentalomas (AIs). Common screening tests for adrenocorticotropin-independent hypercortisolism have substantial false-positive rates, mandating further time and resource-intensive investigations. Objective: To determine whether low basal dehydroepiandrosterone sulfate (DHEAS) is a sensitive and specific screening test for SH in AI. Setting and Patients: In total, 185 patients with AI were screened for adrenal medullary (plasma metanephrines) and cortical [1 mg overnight dexamethasone suppression test (ONDST), 24-hour urinary free cortisol (UFC), serum DHEAS, plasma renin, and aldosterone] hyperfunction. Positive ONDST [1.8 mcg/dL (50 nmol/L)] and/or UFC (more than the upper limit of reference range) results were further investigated. We diagnosed SH when at least 2 of the following were met: raised UFC, raised midnight serum cortisol, 48-hour dexamethasone suppression test (DST) cortisol 1.8 mcg/dL (50 nmol/L). Results: 29 patients (16%)werediagnosedwith SH.Adrenocorticotropinwas,10 pg/mL (,2.2 pmol/L) in all patients with SH. We calculated age-and sex-specific DHEAS ratios (derived by dividing the DHEAS by the lower limit of the respective reference range) for all patients. Receiver operating characteristic curve analyses demonstrated that a ratio of 1.12 was sensitive (.99%) and specific (91.9%) for the diagnosis of SH. Cortisol following 1 mg ONDST of 1.9 mcg/dL (53 nmol/L) was a sensitive (.99%) screening test for SH but had lower specificity (82.9%). The 24-hour UFC lacked sensitivity (69%) and specificity (72%). Conclusion: A single basal measurement of DHEAS offers comparable sensitivity and greater specificity to the existing gold-standard 1mg DST for the detection of SH in patients with AIs.
UR - http://www.scopus.com/inward/record.url?scp=85015147159&partnerID=8YFLogxK
U2 - 10.1210/jc.2016-2718
DO - 10.1210/jc.2016-2718
M3 - Article
C2 - 27797672
AN - SCOPUS:85015147159
SN - 0021-972X
VL - 102
SP - 786
EP - 792
JO - Journal of Clinical Endocrinology and Metabolism
JF - Journal of Clinical Endocrinology and Metabolism
IS - 3
ER -