Adrenal insufficiency.


Journal

Nature reviews. Disease primers
ISSN: 2056-676X
Titre abrégé: Nat Rev Dis Primers
Pays: England
ID NLM: 101672103

Informations de publication

Date de publication:
11 03 2021
Historique:
accepted: 02 02 2021
entrez: 12 3 2021
pubmed: 13 3 2021
medline: 26 11 2021
Statut: epublish

Résumé

Adrenal insufficiency (AI) is a condition characterized by an absolute or relative deficiency of adrenal cortisol production. Primary AI (PAI) is rare and is caused by direct adrenal failure. Secondary AI (SAI) is more frequent and is caused by diseases affecting the pituitary, whereas in tertiary AI (TAI), the hypothalamus is affected. The most prevalent form is TAI owing to exogenous glucocorticoid use. Symptoms of AI are non-specific, often overlooked or misdiagnosed, and are related to the lack of cortisol, adrenal androgen precursors and aldosterone (especially in PAI). Diagnosis is based on measurement of the adrenal corticosteroid hormones, their regulatory peptide hormones and stimulation tests. The goal of therapy is to establish a hormone replacement regimen that closely mimics the physiological diurnal cortisol secretion pattern, tailored to the patient's daily needs. This Primer provides insights into the epidemiology, mechanisms and management of AI during pregnancy as well as challenges of long-term management. In addition, the importance of identifying life-threatening adrenal emergencies (acute AI and adrenal crisis) is highlighted and strategies for prevention, which include patient education, glucocorticoid emergency cards and injection kits, are described.

Identifiants

pubmed: 33707469
doi: 10.1038/s41572-021-00252-7
pii: 10.1038/s41572-021-00252-7
doi:

Substances chimiques

Glucocorticoids 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

19

Subventions

Organisme : Medical Research Council
ID : G0900567
Pays : United Kingdom
Organisme : NIDDK NIH HHS
ID : K23 DK121888
Pays : United States

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Auteurs

Stefanie Hahner (S)

Department of Medicine I, Division of Endocrinology and Diabetology, University Hospital Wuerzburg, Wuerzburg, Germany. Hahner_S@ukw.de.

Richard J Ross (RJ)

Department of Oncology and Metabolism, The University of Sheffield, Sheffield, UK.

Wiebke Arlt (W)

Institute for Metabolism and Systems Research, University of Birmingham, Birmingham, UK.
Centre for Endocrinology, Diabetes, and Metabolism, Birmingham Health Partners, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.

Irina Bancos (I)

Division of Endocrinology, Metabolism and Nutrition, Department of Internal Medicine, Mayo Clinic, Rochester, MN, USA.

Stephanie Burger-Stritt (S)

Department of Medicine I, Division of Endocrinology and Diabetology, University Hospital Wuerzburg, Wuerzburg, Germany.

David J Torpy (DJ)

Endocrine and Metabolic Unit, Royal Adelaide Hospital, University of Adelaide, Adelaide, SA, Australia.

Eystein S Husebye (ES)

Department of Clinical Science, University of Bergen, Bergen, Norway.
K.G. Jebsen Center for Autoimmune Diseases, University of Bergen, Bergen, Norway.
Department of Medicine, Haukeland University Hospital, Bergen, Norway.

Marcus Quinkler (M)

Endocrinology in Charlottenburg, Berlin, Germany.

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