TY - JOUR T1 - Long-chain ω-3 fatty acids for indicated prevention of psychotic disorders: A randomized, placebo-controlled trial AU - Amminger G, Schäfer MR, Papageorgiou K, et al Y1 - 2010/02/01 N1 - 10.1001/archgenpsychiatry.2009.192 JO - Archives of General Psychiatry SP - 146 EP - 154 VL - 67 IS - 2 N2 - Context  The use of antipsychotic medication for the prevention of psychotic disorders is controversial. Long-chain ω-3 (omega-3) polyunsaturated fatty acids (PUFAs) may be beneficial in a range of psychiatric conditions, including schizophrenia. Given that ω-3 PUFAs are generally beneficial to health and without clinically relevant adverse effects, their preventive use in psychosis merits investigation.Objective  To determine whether ω-3 PUFAs reduce the rate of progression to first-episode psychotic disorder in adolescents and young adults aged 13 to 25 years with subthreshold psychosis.Design  Randomized, double-blind, placebo-controlled trial conducted between 2004 and 2007.Setting  Psychosis detection unit of a large public hospital in Vienna, Austria.Participants  Eighty-one individuals at ultra-high risk of psychotic disorder.Interventions  A 12-week intervention period of 1.2-g/d ω-3 PUFA or placebo was followed by a 40-week monitoring period; the total study period was 12 months.Main Outcome Measures  The primary outcome measure was transition to psychotic disorder. Secondary outcomes included symptomatic and functional changes. The ratio of ω-6 to ω-3 fatty acids in erythrocytes was used to index pretreatment vs posttreatment fatty acid composition.Results  Seventy-six of 81 participants (93.8%) completed the intervention. By study's end (12 months), 2 of 41 individuals (4.9%) in the ω-3 group and 11 of 40 (27.5%) in the placebo group had transitioned to psychotic disorder (P = .007). The difference between the groups in the cumulative risk of progression to full-threshold psychosis was 22.6% (95% confidence interval, 4.8-40.4). ω-3 Polyunsaturated fatty acids also significantly reduced positive symptoms (P = .01), negative symptoms (P = .02), and general symptoms (P = .01) and improved functioning (P = .002) compared with placebo. The incidence of adverse effects did not differ between the treatment groups.Conclusions  Long-chain ω-3 PUFAs reduce the risk of progression to psychotic disorder and may offer a safe and efficacious strategy for indicated prevention in young people with subthreshold psychotic states.Trial Registration  clinicaltrials.gov Identifier: NCT00396643 SN - 0003-990X M3 - doi: 10.1001/archgenpsychiatry.2009.192 UR - http://dx.doi.org/10.1001/archgenpsychiatry.2009.192 ER -