Long-Chain ω-3 Fatty Acids for Indicated Prevention of Psychotic Disorders A Randomized, Placebo-Controlled Trial

被引:649
作者
Amminger, G. Paul [1 ,2 ]
Schafer, Miriam R. [1 ]
Papageorgiou, Konstantinos [1 ]
Klier, Claudia M. [1 ]
Cotton, Sue M. [2 ]
Harrigan, Susan M. [2 ]
Mackinnon, Andrew [2 ]
McGorry, Patrick D. [2 ]
Berger, Gregor E. [3 ]
机构
[1] Med Univ Vienna, Dept Child & Adolescent Psychiat, Vienna, Austria
[2] Univ Melbourne, Ctr Youth Mental Hlth, Orygen Res Ctr, Melbourne, Vic, Australia
[3] Schlossli Clin, Dept Res & Educ, Oetwil Am See, Switzerland
关键词
ETHYL-EICOSAPENTAENOIC ACID; 1ST-EPISODE PSYCHOSIS; IMPAIRMENT; DEPRESSION; SYMPTOMS; RISK; SCHIZOPHRENIA; ABNORMALITIES; PEOPLE; FUTURE;
D O I
10.1001/archgenpsychiatry.2009.192
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Context: The use of antipsychotic medication for the prevention of psychotic disorders is controversial. Long-chain omega-3 (omega-3) polyunsaturated fatty acids (PUFAs) may be beneficial in a range of psychiatric conditions, including schizophrenia. Given that omega-3 PUFAs are generally beneficial to health and without clinically relevant adverse effects, their preventive use in psychosis merits investigation. Objective: To determine whether omega-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 1.2g/d omega-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 omega-6 to omega-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 omega-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). omega-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 omega-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.
引用
收藏
页码:146 / 154
页数:9
相关论文
共 41 条
[31]   Two double-blind placebo-controlled pilot studies of eicosapentaenoic acid in the treatment of schizophrenia [J].
Peet, M ;
Brind, J ;
Ramchand, CN ;
Shah, S ;
Vankar, GK .
SCHIZOPHRENIA RESEARCH, 2001, 49 (03) :243-251
[32]   A dose-ranging exploratory study of the effects of ethyl-eicosapentaenoate in patients with persistent schizophrenic symptoms [J].
Peet, M ;
Horrobin, DF .
JOURNAL OF PSYCHIATRIC RESEARCH, 2002, 36 (01) :7-18
[33]   A dose-ranging study of the, effects of ethyl-eicosapentaenoate in patients with ongoing depression despite apparently adequate treatment with standard drugs [J].
Peet, M ;
Horrobin, DF .
ARCHIVES OF GENERAL PSYCHIATRY, 2002, 59 (10) :913-919
[34]   DOPAMINE ACTIVATION OF THE ARACHIDONIC-ACID CASCADE AS A BASIS FOR D1/D2 RECEPTOR SYNERGISM [J].
PIOMELLI, D ;
PILON, C ;
GIROS, B ;
SOKOLOFF, P ;
MARTRES, MP ;
SCHWARTZ, JC .
NATURE, 1991, 353 (6340) :164-167
[35]   Children's self-reported psychotic symptoms and adult schizophreniform disorder -: A 15-year longitudinal study [J].
Poulton, R ;
Caspi, A ;
Moffitt, TE ;
Cannon, M ;
Murray, R ;
Harrington, H .
ARCHIVES OF GENERAL PSYCHIATRY, 2000, 57 (11) :1053-1058
[36]   Mitochondrial dysfunction in schizophrenia: evidence for compromised brain metabolism and oxidative stress [J].
Prabakaran, S ;
Swatton, JE ;
Ryan, MM ;
Huffaker, SJ ;
Huang, JTJ ;
Griffin, JL ;
Wayland, M ;
Freeman, T ;
Dudbridge, F ;
Lilley, KS ;
Karp, NA ;
Hester, S ;
Tkachev, D ;
Mimmack, ML ;
Yolken, RH ;
Webster, MJ ;
Torrey, EF ;
Bahn, S .
MOLECULAR PSYCHIATRY, 2004, 9 (07) :684-697
[37]   Synaptic plasticity impairment and hypofunction of NMDA receptors induced by glutathione deficit:: Relevance to schizophrenia [J].
Steullet, P ;
Neijt, HC ;
Cuénod, M ;
Do, KQ .
NEUROSCIENCE, 2006, 137 (03) :807-819
[38]   Prevalence of psychotic disorder and community level of psychotic symptoms -: An urban-rural comparison [J].
van Os, J ;
Hanssen, M ;
Bijl, RV ;
Vollebergh, W .
ARCHIVES OF GENERAL PSYCHIATRY, 2001, 58 (07) :663-668
[39]   A systematic review and meta-analysis of the psychosis continuum: evidence for a psychosis proneness-persistence-impairment model of psychotic disorder [J].
van Os, J. ;
Linscott, R. J. ;
Myin-Germeys, I. ;
Delespaul, P. ;
Krabbendam, L. .
PSYCHOLOGICAL MEDICINE, 2009, 39 (02) :179-195
[40]  
Yung AR, 2007, MED J AUSTRALIA, V187, pS43