Diagnostic testing of autonomous cortisol secretion in adrenal incidentalomas

Objective: Autonomous cortisol secretion (ACS) is a condition with ACTH-independent cortisol overproduction from adrenal incidentalomas (AI) or adrenal hyperplasia. The hypercortisolism is often mild, and most patients lack typical clinical features of overt Cushing’s syndrome (CS). ACS is not well...

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Main Authors: Grethe Å Ueland, Thea Grinde, Paal Methlie, Oskar Kelp, Kristian Løvås, Eystein S Husebye
Format: Article
Language:English
Published: Bioscientifica 2020-10-01
Series:Endocrine Connections
Subjects:
Online Access:https://ec.bioscientifica.com/view/journals/ec/9/10/EC-20-0419.xml
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spelling doaj-8f3f40495aca4f87a8ef467cf2187a522020-11-25T03:37:06ZengBioscientificaEndocrine Connections2049-36142049-36142020-10-01910963970https://doi.org/10.1530/EC-20-0419Diagnostic testing of autonomous cortisol secretion in adrenal incidentalomasGrethe Å Ueland0Thea Grinde1Paal Methlie2Oskar Kelp3Kristian Løvås4Eystein S Husebye5Department of Clinical Science, University of Bergen, Bergen, Norway; Department of Medicine, Haukeland University Hospital, Bergen, NorwayDepartment of Clinical Science, University of Bergen, Bergen, NorwayDepartment of Clinical Science, University of Bergen, Bergen, Norway; Department of Medicine, Haukeland University Hospital, Bergen, Norway; K. G. Jebsen Center for Autoimmune Disorders, University of Bergen, Bergen, NorwayDepartment of Medicine, Akershus University Hospital, Nordbyhagen, NorwayDepartment of Medicine, Haukeland University Hospital, Bergen, Norway; K. G. Jebsen Center for Autoimmune Disorders, University of Bergen, Bergen, NorwayDepartment of Clinical Science, University of Bergen, Bergen, Norway; Department of Medicine, Haukeland University Hospital, Bergen, Norway; K. G. Jebsen Center for Autoimmune Disorders, University of Bergen, Bergen, NorwayObjective: Autonomous cortisol secretion (ACS) is a condition with ACTH-independent cortisol overproduction from adrenal incidentalomas (AI) or adrenal hyperplasia. The hypercortisolism is often mild, and most patients lack typical clinical features of overt Cushing’s syndrome (CS). ACS is not well defined and diagnostic tests lack validation. Methods: Retrospective study of 165 patients with AI evaluated clinically and by assay of morning plasma ACTH, late-night saliva cortisol, serum DHEA sulphate (DHEAS), 24-h urine-free cortisol, and cortisol after dexamethasone suppression. Results: Patients with AI (n = 165) were diagnosed as non-functioning incidentalomas (NFI) (n = 82) or ACS (n = 83) according to current European guidelines. Late-night saliv a cortisol discriminated poorly between NFI and ACS, showing a high rate of false-positive (23/63) and false-negative (38/69) results. The conventional lo w-dose dexamethasone suppression test (LDDST) did not improve the diagnostic specific ity, compared with the 1 mg overnight DST. Receiver operating characteristic curve analysis of DHEAS in the two cohorts demonstrated an area under the curve of 0.76 (P < 0.01) with a sensitivity for ACS of 58% and a specificity of 80% using the recommended cutoff at 1.04 μmol/L (40 μg/dL). Conclusion: We here demonstrate in a large retrospective cohort of incidentaloma patients, that neither DHEAS, late-night saliva cortisol nor 24-h urine free cortisol are useful to discriminate between non-functioning adrenal incidentalomas and ACS. The conventional LDDST do not add further information compared with the 1 mg ove rnight DST. Alternative biomarkers are needed to improve the diagnostic workup of ACS. https://ec.bioscientifica.com/view/journals/ec/9/10/EC-20-0419.xmlautonomous cortisol secretionadrenal incidentalomacushing’s syndromedheassaliva cortisol
collection DOAJ
language English
format Article
sources DOAJ
author Grethe Å Ueland
Thea Grinde
Paal Methlie
Oskar Kelp
Kristian Løvås
Eystein S Husebye
spellingShingle Grethe Å Ueland
Thea Grinde
Paal Methlie
Oskar Kelp
Kristian Løvås
Eystein S Husebye
Diagnostic testing of autonomous cortisol secretion in adrenal incidentalomas
Endocrine Connections
autonomous cortisol secretion
adrenal incidentaloma
cushing’s syndrome
dheas
saliva cortisol
author_facet Grethe Å Ueland
Thea Grinde
Paal Methlie
Oskar Kelp
Kristian Løvås
Eystein S Husebye
author_sort Grethe Å Ueland
title Diagnostic testing of autonomous cortisol secretion in adrenal incidentalomas
title_short Diagnostic testing of autonomous cortisol secretion in adrenal incidentalomas
title_full Diagnostic testing of autonomous cortisol secretion in adrenal incidentalomas
title_fullStr Diagnostic testing of autonomous cortisol secretion in adrenal incidentalomas
title_full_unstemmed Diagnostic testing of autonomous cortisol secretion in adrenal incidentalomas
title_sort diagnostic testing of autonomous cortisol secretion in adrenal incidentalomas
publisher Bioscientifica
series Endocrine Connections
issn 2049-3614
2049-3614
publishDate 2020-10-01
description Objective: Autonomous cortisol secretion (ACS) is a condition with ACTH-independent cortisol overproduction from adrenal incidentalomas (AI) or adrenal hyperplasia. The hypercortisolism is often mild, and most patients lack typical clinical features of overt Cushing’s syndrome (CS). ACS is not well defined and diagnostic tests lack validation. Methods: Retrospective study of 165 patients with AI evaluated clinically and by assay of morning plasma ACTH, late-night saliva cortisol, serum DHEA sulphate (DHEAS), 24-h urine-free cortisol, and cortisol after dexamethasone suppression. Results: Patients with AI (n = 165) were diagnosed as non-functioning incidentalomas (NFI) (n = 82) or ACS (n = 83) according to current European guidelines. Late-night saliv a cortisol discriminated poorly between NFI and ACS, showing a high rate of false-positive (23/63) and false-negative (38/69) results. The conventional lo w-dose dexamethasone suppression test (LDDST) did not improve the diagnostic specific ity, compared with the 1 mg overnight DST. Receiver operating characteristic curve analysis of DHEAS in the two cohorts demonstrated an area under the curve of 0.76 (P < 0.01) with a sensitivity for ACS of 58% and a specificity of 80% using the recommended cutoff at 1.04 μmol/L (40 μg/dL). Conclusion: We here demonstrate in a large retrospective cohort of incidentaloma patients, that neither DHEAS, late-night saliva cortisol nor 24-h urine free cortisol are useful to discriminate between non-functioning adrenal incidentalomas and ACS. The conventional LDDST do not add further information compared with the 1 mg ove rnight DST. Alternative biomarkers are needed to improve the diagnostic workup of ACS.
topic autonomous cortisol secretion
adrenal incidentaloma
cushing’s syndrome
dheas
saliva cortisol
url https://ec.bioscientifica.com/view/journals/ec/9/10/EC-20-0419.xml
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