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Tuesday's Bipolar Abstract:
Omega-3 Fatty Acids for Major
Depressive Disorder During Pregnancy: Results From a Randomized,
Double-Blind, Placebo-Controlled Trial
Kuan-Pin Su, Shih-Yi
Huang, Tsan-Hung Chiu, Kuo-Cherh Huang, Chieh-Liang Huang, Hui-Chih
Chang, and Carmine M. Pariante
From the Department of
Psychiatry and Mind-Body Interface Research Centre (Drs. Su and C-L
Huang) and the Department of Obstetrics and Gynecology (Dr. Chiu), China
Medical University Hospital, Taichung, Taiwan; the School of Nutrition
and Health Sciences (Drs. Su and S-Y Huang) and the School of Health
Care Administration (Drs. K-C Huang and Chang), Taipei Medical
University, Taipei, Taiwan; and the Institute of Psychiatry, King's
College London, United Kingdom (Drs. Su and Pariante and Ms. Chang)
Objective: Perinatal
depression is common, and treatment remains challenging. Depression has
been reported to be associated with the abnormality of omega-3
polyunsaturated fatty acids (PUFAs). A profound decrease of omega-3
PUFAs in the mother during pregnancy is associated with the higher
demand of fetal development and might precipitate the occurrence of
depression. In this study, we examined the efficacy of omega-3 PUFA
monotherapy for the treatment of depression during pregnancy.
Methods:
From June 2004 to June 2006, we conducted an 8-week, double-blind,
placebo-controlled trial comparing omega-3 PUFAs (3.4 g/d) with placebo
in pregnant women with major depressive disorder (DSM-IV criteria). No
psychotropic agent was given 1 month prior to or during the study
period. The Hamilton Rating Scale for Depression (HAM-D) was scored
every other week as the primary measurement of efficacy, while the
Edinburgh Postnatal Depression Scale (EPDS) and Beck Depression
Inventory (BDI) were secondary measures.
Results: Thirty-six subjects
were randomly assigned to either omega-3 PUFAs or placebo, and 33 among
them were evaluated in more than 2 visits. A total of 24 subjects
completed the study. As compared to the placebo group, subjects in the
omega-3 group had significantly lower HAM-D scores at weeks 6 (p = .001)
and 8 (p = .019), a significantly higher response rate (62% vs. 27%, p =
.03), and a higher remission rate, although the latter did not reach
statistical significance (38% vs. 18%, p = .28). At the study end point,
subjects in the omega-3 group also had significantly lower depressive
symptom ratings on the EPDS and BDI. The omega-3 PUFAs were well
tolerated and there were no adverse effects on the subjects and
newborns.
Conclusions: Omega-3 PUFAs may have therapeutic
benefits in depression during pregnancy. In regard to the safety issue
and psychotherapeutic effect, as well as health promotion to mothers and
their newborns, it is worthy to conduct replication studies in a larger
sample with a broad regimen of omega-3 PUFAs in pregnant women with
depression.
Source:
Journal of
Clinical Psychiatry
March 18, 2008: Epub ahead of print
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Other
bipolar Links:

Juvenile Bipolar
Research Foundation

Child and Adolescent
Bipolar Foundation

Depression and
Bipolar
Support Alliance

NIMH Child and
Adolescent Mental Health

International Society for Bipolar Disorders
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