A 52-week prophylactic randomised control trial of omega-3 polyunsaturated fatty acids in bipolar disorder.


Journal

Bipolar disorders
ISSN: 1399-5618
Titre abrégé: Bipolar Disord
Pays: Denmark
ID NLM: 100883596

Informations de publication

Date de publication:
11 2021
Historique:
pubmed: 20 12 2020
medline: 20 4 2022
entrez: 19 12 2020
Statut: ppublish

Résumé

Previous work suggests supplementation with omega-3 polyunsaturated fatty acids (PUFAs) may improve mood symptoms in bipolar disorder (BD) although findings remain unclear. In this study, we assess the efficacy of omega-3 PUFA administration for prophylaxis in BD using a clinical trial design over 52-weeks (ClinicalTrials.gov Identifier: NCT04210804). Individuals with BD (n = 80) were randomised to receive placebo (n = 40) or 1 g eicosapentaenoic acid (EPA) plus 1 g docosahexaenoic acid (DHA; n = 40) adjunctively for 52-weeks. The primary outcome measure comprised the number of mood episode relapses including hospital admissions and medication changes experienced. Secondary outcome measures included time to first mood episode relapse and change in psychometric measures of depression and elation (Hamilton Depression Rating Scale and Young Mania Rating Scale). No significant differences in the number of mood episode relapses (U = 490.00, p = 0.14) or the number of individuals requiring admission to hospital (χ Despite a minor reduction in hypomania scores in the omega-3 PUFA group compared to placebo, we find little evidence that the supplementation of omega-3-PUFAs exhibits prophylactic benefit in BD.

Identifiants

pubmed: 33340432
doi: 10.1111/bdi.13037
doi:

Substances chimiques

Fatty Acids, Omega-3 0
Docosahexaenoic Acids 25167-62-8
Eicosapentaenoic Acid AAN7QOV9EA

Banques de données

ClinicalTrials.gov
['NCT04210804']

Types de publication

Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

697-706

Informations de copyright

© 2020 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Références

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Auteurs

Genevieve McPhilemy (G)

The Centre for Neuroimaging & Cognitive Genomics (NICOG), Clinical Neuroimaging Lab, NCBES Galway Neuroscience Centre, College of Medicine, Nursing, and Health Sciences, National University of Ireland Galway, Galway Ireland, Republic of Ireland.
Health Research Board - Clinical Research Facility Galway, National University of Ireland Galway and University Hospital Galway, Galway, Ireland.

Fintan Byrne (F)

The Centre for Neuroimaging & Cognitive Genomics (NICOG), Clinical Neuroimaging Lab, NCBES Galway Neuroscience Centre, College of Medicine, Nursing, and Health Sciences, National University of Ireland Galway, Galway Ireland, Republic of Ireland.

Mairead Waldron (M)

Health Research Board - Clinical Research Facility Galway, National University of Ireland Galway and University Hospital Galway, Galway, Ireland.

Joseph R Hibbeln (JR)

Section on Nutritional Neurosciences, Laboratory of Membrane Biochemistry and Biophysics, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Rockville, MD, USA.

John Davis (J)

Department of Psychiatry, University of Illinois, Chicago, USA.

Colm McDonald (C)

The Centre for Neuroimaging & Cognitive Genomics (NICOG), Clinical Neuroimaging Lab, NCBES Galway Neuroscience Centre, College of Medicine, Nursing, and Health Sciences, National University of Ireland Galway, Galway Ireland, Republic of Ireland.
Health Research Board - Clinical Research Facility Galway, National University of Ireland Galway and University Hospital Galway, Galway, Ireland.

Brian Hallahan (B)

The Centre for Neuroimaging & Cognitive Genomics (NICOG), Clinical Neuroimaging Lab, NCBES Galway Neuroscience Centre, College of Medicine, Nursing, and Health Sciences, National University of Ireland Galway, Galway Ireland, Republic of Ireland.
Health Research Board - Clinical Research Facility Galway, National University of Ireland Galway and University Hospital Galway, Galway, Ireland.

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