Circadian depression: A mood disorder phenotype.

Bipolar disorder Circadian rhythms Depression Mood disorders Sleep-wake cycles

Journal

Neuroscience and biobehavioral reviews
ISSN: 1873-7528
Titre abrégé: Neurosci Biobehav Rev
Pays: United States
ID NLM: 7806090

Informations de publication

Date de publication:
07 2021
Historique:
received: 06 08 2020
revised: 18 02 2021
accepted: 28 02 2021
pubmed: 11 3 2021
medline: 29 6 2021
entrez: 10 3 2021
Statut: ppublish

Résumé

Major mood syndromes are among the most common and disabling mental disorders. However, a lack of clear delineation of their underlying pathophysiological mechanisms is a major barrier to prevention and optimised treatments. Dysfunction of the 24-h circadian system is a candidate mechanism that has genetic, behavioural, and neurobiological links to mood syndromes. Here, we outline evidence for a new clinical phenotype, which we have called 'circadian depression'. We propose that key clinical characteristics of circadian depression include disrupted 24-h sleep-wake cycles, reduced motor activity, low subjective energy, and weight gain. The illness course includes early age-of-onset, phenomena suggestive of bipolarity (defined by bidirectional associations between objective motor and subjective energy/mood states), poor response to conventional antidepressant medications, and concurrent cardiometabolic and inflammatory disturbances. Identifying this phenotype could be clinically valuable, as circadian-targeted strategies show promise for reducing depressive symptoms and stabilising illness course. Further investigation of underlying circadian disturbances in mood syndromes is needed to evaluate the clinical utility of this phenotype and guide the optimal use of circadian-targeted interventions.

Identifiants

pubmed: 33689801
pii: S0149-7634(21)00107-X
doi: 10.1016/j.neubiorev.2021.02.045
pii:
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

79-101

Subventions

Organisme : Intramural NIH HHS
ID : Z01 MH002804
Pays : United States

Informations de copyright

Copyright © 2021. Published by Elsevier Ltd.

Auteurs

Joanne S Carpenter (JS)

Youth Mental Health and Technology Team, Brain & Mind Centre, The University of Sydney, Camperdown, Australia.

Jacob J Crouse (JJ)

Youth Mental Health and Technology Team, Brain & Mind Centre, The University of Sydney, Camperdown, Australia.

Elizabeth M Scott (EM)

Youth Mental Health and Technology Team, Brain & Mind Centre, The University of Sydney, Camperdown, Australia; School of Medicine, University of Notre Dame, Sydney, Australia.

Sharon L Naismith (SL)

Youth Mental Health and Technology Team, Brain & Mind Centre, The University of Sydney, Camperdown, Australia; Charles Perkins Centre, University of Sydney, Sydney, New South Wales, Australia; School of Psychology, University of Sydney, Sydney, New South Wales, Australia.

Chloe Wilson (C)

Youth Mental Health and Technology Team, Brain & Mind Centre, The University of Sydney, Camperdown, Australia.

Jan Scott (J)

Youth Mental Health and Technology Team, Brain & Mind Centre, The University of Sydney, Camperdown, Australia; Academic Psychiatry, Institute of Neuroscience, Newcastle University, UK; Diderot University, Sorbonne City, Paris, France; Department of Mental Health, Norwegian University of Science and Technology, Trondheim, Norway.

Kathleen R Merikangas (KR)

Genetic Epidemiology Research Branch, Intramural Research Program, National Institute of Mental Health, Bethesda, USA.

Ian B Hickie (IB)

Youth Mental Health and Technology Team, Brain & Mind Centre, The University of Sydney, Camperdown, Australia. Electronic address: ian.hickie@sydney.edu.au.

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Classifications MeSH