Page 54 - Complementary and Alternative Medicine Treatments in Psychiatry
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54  |  Complementary and Alternative Medicine Treatments in Psychiatry

          prophylactic effect against psychosis. Researchers in Austria
          treated young patients, aged 13 to 25, who were at ultra-high
          risk for psychotic disorder, in a twelve-week, double-blind study.
          This was followed by a 40-week monitoring period. The EFA
          group received 1.2 grams a day of omega-3 fatty acids. At the end
          of the study, among the EFA group only 2 of 41 individuals had
          transitioned to psychotic disorder compared to 11 of 40 in the
          placebo group (Amminger 2010).

          Fatty Acids and Depression

          As good as the news has been with EFA treatment of psychotic
          disorders, a stream of studies has consistently shown the
          effectiveness of omega-3s in the treatment of depression, so
          much so that it has become a mainstay therapy in many private
          practices and hospitals.
           As an example of the effectiveness of EFAs in a broad range of
          depressive clients, researchers in Israel reviewed three clinical
          trials carried out on a variety of patient populations at Beer
          Sheva Mental Health Center. The first tested EPA versus placebo
          on 20 unipolar clients with major depression as an adjunct to
          antidepressant therapy. The second study treated 28 children,
          ages 6–12, with a monotherapy of EPA or placebo. The third
          study treated 12 bipolar patients with an open-label, add-on trial
          of 1.5 to 2 grams per day of EPA for up to 6 months.
           Results were very good across the board. The unipolar group
          showed “highly significant benefits” by week three. The child
          study showed, again, “highly significant effects of omega-3” on
          each of the three rating scales. Of the participants in the bipolar
          study, 8 of 10 who completed at least one month of follow-up
          achieved a 50% or greater reduction in Hamilton depression
          scores within one month. No significant side effects were
          reported in any of the studies (Osher 2009).
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