2001
DOI: 10.1176/appi.ajp.158.12.2071
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A Placebo-Controlled Trial of Omega-3 Fatty Acid (Ethyl Eicosapentaenoic Acid) Supplementation for Residual Symptoms and Cognitive Impairment in Schizophrenia

Abstract: For schizophrenia patients treated with 3 g/day of ethyl EPA, improvement in residual symptoms and cognitive impairment was no greater than for schizophrenia patients treated with placebo.

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Cited by 282 publications
(130 citation statements)
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“…Controlled clinical trials in established schizophrenia indicate that either sole or augmentation therapy with omega-3 fatty acids may be beneficial (Emsley et al, 2002;Joy et al, 2006;Mellor et al, 1996;Peet et al, 2001), with some conflicting results (Emsley et al, 2006;Fenton et al, 2001;Peet and Horrobin, 2002a, b). Furthermore, controlled clinical trials in treatment-resistant depression (Nemets et al, 2002;Peet and Horrobin, 2002a, b), bipolar depression (Keck et al, 2006), bipolar affective disorder (Stoll et al, 1999), borderline personality disorder (Zanarini and Frankenburg, 2003), incarcerated young males (Gesch et al, 2002), and children with developmental coordination disorders (Richardson and Montgomery, 2005) also suggest that omega-3 fatty acids may modulate mood, impulsivity, and aggression, while potential neuroprotective effects were found in Huntington's disease (Puri et al, 2002(Puri et al, , 2005.…”
Section: Introductionmentioning
confidence: 99%
“…Controlled clinical trials in established schizophrenia indicate that either sole or augmentation therapy with omega-3 fatty acids may be beneficial (Emsley et al, 2002;Joy et al, 2006;Mellor et al, 1996;Peet et al, 2001), with some conflicting results (Emsley et al, 2006;Fenton et al, 2001;Peet and Horrobin, 2002a, b). Furthermore, controlled clinical trials in treatment-resistant depression (Nemets et al, 2002;Peet and Horrobin, 2002a, b), bipolar depression (Keck et al, 2006), bipolar affective disorder (Stoll et al, 1999), borderline personality disorder (Zanarini and Frankenburg, 2003), incarcerated young males (Gesch et al, 2002), and children with developmental coordination disorders (Richardson and Montgomery, 2005) also suggest that omega-3 fatty acids may modulate mood, impulsivity, and aggression, while potential neuroprotective effects were found in Huntington's disease (Puri et al, 2002(Puri et al, , 2005.…”
Section: Introductionmentioning
confidence: 99%
“…Their study could only show important and statistically significant beneficial effects of 2 g daily EPA in the presence of clozapine, while their placebo group receiving antipsychotics alone also showed a positive response. Further, Fenton and others, researching a relatively large cohort of 75 subjects with schizophrenia, could find no effect of 3 g daily ethyl-EPA on all ratings measured (84). As stated in a recent review by Joy and others (85), more results are urgently needed before fish oil or ethyl-EPA can be regarded as beneficial in the treatment of schizophrenia.…”
Section: Psychological Stressmentioning
confidence: 96%
“…Alternatively, the 'cAMP signal transduction hypothesis' suggests depression to be caused by impaired phospholipid metabolism and impaired FA-related signal transduction (due to inadequate intake of fish and n-3 FA) and may also explain the association between depression and CVD (46) . There have been small clinical trials based in developed countries (USA, Israel and the UK) examining the impact on depressed patients of FA supplementation but results are varied, with some studies showing an improvement in depressive symptoms following FA supplementation (47)(48)(49) and others not (50) .…”
Section: Strengths and Limitations Of The Studymentioning
confidence: 99%