TY - JOUR
T1 - Baseline blood levels of omega-3 and depression remission
T2 - A secondary analysis of data from a placebo-controlled trial of omega-3 supplements
AU - Carney, Robert M.
AU - Steinmeyer, Brian C.
AU - Freedland, Kenneth E.
AU - Rubin, Eugene H.
AU - Rich, Michael W.
AU - Harris, William S.
N1 - Funding Information:
Dr Carney has received grant/research support from the National Institutes of Health, and he or a member of his family owns stock in Pfizer. Dr Harris is the President of OmegaQuant Analytics; is a Senior Research Scientist at Health Diagnostic Laboratory; and is a consultant for Omthera Pharmaceuticals, Aker Biomarine Antarctica, and Tersus Pharmaceuticals. The remaining authors report no potential conflicts of interest. Funding/support: This study was supported in part by Grants R01 HL076808 and R01 HL117805 from the National Heart, Lung, and Blood Institute (Dr Carney, principal investigator). Glaxo-Smith-Kline (formally Reliant) provided Lovaza (omega-3) and placebo capsules, and Pfizer provided Zoloft (sertraline) for this study.
Publisher Copyright:
© 2015 Copyright Physicians Postgraduate Press, Inc.
PY - 2016/2
Y1 - 2016/2
N2 - Objective: Depression is associated with low red blood cell (RBC) levels of 2 omega-3 fatty acids, eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), suggesting that omega-3 supplements might improve depression. However, clinical trials have produced mixed results. The purpose of this secondary analysis of data from a randomized controlled trial was to determine whether baseline blood levels of omega-3, which are known to vary widely among individuals, predict depression outcomes. Method: The percentages of EPA, DHA, and the omega-6 arachidonic acid (AA) were measured in RBCs at baseline and posttreatment in 122 participants with DSM-IV major depression who were randomly assigned between May 2005 and December 2008 to receive either 50 mg/d of sertraline and a daily dosage of 930 mg EPA/750 mg DHA or sertraline plus placebo. Associations between baseline omega-3 RBC levels and remission of depression (17-item Hamilton Depression Rating Scale score = 7) were analyzed by treatment arm. Results: Among participants in the omega-3 arm, baseline RBC levels of EPA + DHA (P = .002) and the EPA + DHA:AA ratio (P = .003) were significantly higher among those whose depression subsequently remitted compared with those whose depression did not remit. No associations were detected in the sertraline plus placebo arm. Baseline levels of EPA (P = .03) and the EPA + DHA:AA ratio (P = .04) moderated the relationship between treatment arm and depression outcomes. Conclusions: High baseline RBC levels of EPA and DHA and a high EPA + DHA:AA ratio predict favorable depression outcomes in patients receiving omega-3 supplements. Omega-3 supplementation may be an effective treatment for depression, but the requisite dosage and duration of treatment may depend on the patient's baseline level of omega-3 fatty acids.
AB - Objective: Depression is associated with low red blood cell (RBC) levels of 2 omega-3 fatty acids, eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), suggesting that omega-3 supplements might improve depression. However, clinical trials have produced mixed results. The purpose of this secondary analysis of data from a randomized controlled trial was to determine whether baseline blood levels of omega-3, which are known to vary widely among individuals, predict depression outcomes. Method: The percentages of EPA, DHA, and the omega-6 arachidonic acid (AA) were measured in RBCs at baseline and posttreatment in 122 participants with DSM-IV major depression who were randomly assigned between May 2005 and December 2008 to receive either 50 mg/d of sertraline and a daily dosage of 930 mg EPA/750 mg DHA or sertraline plus placebo. Associations between baseline omega-3 RBC levels and remission of depression (17-item Hamilton Depression Rating Scale score = 7) were analyzed by treatment arm. Results: Among participants in the omega-3 arm, baseline RBC levels of EPA + DHA (P = .002) and the EPA + DHA:AA ratio (P = .003) were significantly higher among those whose depression subsequently remitted compared with those whose depression did not remit. No associations were detected in the sertraline plus placebo arm. Baseline levels of EPA (P = .03) and the EPA + DHA:AA ratio (P = .04) moderated the relationship between treatment arm and depression outcomes. Conclusions: High baseline RBC levels of EPA and DHA and a high EPA + DHA:AA ratio predict favorable depression outcomes in patients receiving omega-3 supplements. Omega-3 supplementation may be an effective treatment for depression, but the requisite dosage and duration of treatment may depend on the patient's baseline level of omega-3 fatty acids.
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U2 - 10.4088/JCP.14m09660
DO - 10.4088/JCP.14m09660
M3 - Article
C2 - 26930527
AN - SCOPUS:84959534486
SN - 0160-6689
VL - 77
SP - e138-e143
JO - Journal of Clinical Psychiatry
JF - Journal of Clinical Psychiatry
IS - 2
ER -