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Neurobiological and behavioral mechanisms of circadian rhythm disruption in bipolar disorder: A critical multi-disciplinary literature review and agenda for future research from the ISBD task force on chronobiology

Journal

BIPOLAR DISORDERS
Volume 24, Issue 3, Pages 232-263

Publisher

WILEY
DOI: 10.1111/bdi.13165

Keywords

actigraphy; animal models; biomarker; chronobiology; circadian; clock gene; levels of analysis; light; lithium; sleep

Funding

  1. VA Merit Award [BX003431]
  2. NCCIH [K99 AT010903]
  3. Kavli Institute for Brain and Mind
  4. German Research Foundation
  5. Emmy Noether Fellowship [LA4126/1-1]
  6. NIMH [MH077908, MH102310, MH126911]

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Symptoms of bipolar disorder include changes in mood, activity, energy, sleep, and appetite, with circadian rhythm disturbance considered a biological feature underlying BD. Research has found associations between the circadian system and mood regulation, but circadian disruption is not specific to BD and is present across various psychiatric disorders. Future studies on circadian rhythms and its role in BD should carefully define associations and integrate across levels of analysis for more comprehensive insights.
Aim Symptoms of bipolar disorder (BD) include changes in mood, activity, energy, sleep, and appetite. Since many of these processes are regulated by circadian function, circadian rhythm disturbance has been examined as a biological feature underlying BD. The International Society for Bipolar Disorders Chronobiology Task Force (CTF) was commissioned to review evidence for neurobiological and behavioral mechanisms pertinent to BD. Method Drawing upon expertise in animal models, biomarkers, physiology, and behavior, CTF analyzed the relevant cross-disciplinary literature to precisely frame the discussion around circadian rhythm disruption in BD, highlight key findings, and for the first time integrate findings across levels of analysis to develop an internally consistent, coherent theoretical framework. Results Evidence from multiple sources implicates the circadian system in mood regulation, with corresponding associations with BD diagnoses and mood-related traits reported across genetic, cellular, physiological, and behavioral domains. However, circadian disruption does not appear to be specific to BD and is present across a variety of high-risk, prodromal, and syndromic psychiatric disorders. Substantial variability and ambiguity among the definitions, concepts and assumptions underlying the research have limited replication and the emergence of consensus findings. Conclusions Future research in circadian rhythms and its role in BD is warranted. Well-powered studies that carefully define associations between BD-related and chronobiologically-related constructs, and integrate across levels of analysis will be most illuminating.

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