TY - JOUR
T1 - Neurobiological and behavioral mechanisms of circadian rhythm disruption in bipolar disorder
T2 - A critical multi-disciplinary literature review and agenda for future research from the ISBD task force on chronobiology
AU - McCarthy, Michael J.
AU - Gottlieb, John F.
AU - Gonzalez, Robert
AU - McClung, Colleen A.
AU - Alloy, Lauren B.
AU - Cain, Sean
AU - Dulcis, Davide
AU - Etain, Bruno
AU - Frey, Benicio N.
AU - Garbazza, Corrado
AU - Ketchesin, Kyle D.
AU - Landgraf, Dominic
AU - Lee, Heon Jeong
AU - Marie-Claire, Cynthia
AU - Nusslock, Robin
AU - Porcu, Alessandra
AU - Porter, Richard
AU - Ritter, Philipp
AU - Scott, Jan
AU - Smith, Daniel
AU - Swartz, Holly A.
AU - Murray, Greg
N1 - Publisher Copyright:
© 2021 The Authors. Bipolar Disorders published by John Wiley & Sons Ltd.
PY - 2022/5
Y1 - 2022/5
N2 - 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.
AB - 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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U2 - 10.1111/bdi.13165
DO - 10.1111/bdi.13165
M3 - Review article
C2 - 34850507
AN - SCOPUS:85120881756
SN - 1398-5647
VL - 24
SP - 232
EP - 263
JO - Bipolar Disorders
JF - Bipolar Disorders
IS - 3
ER -