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. 2024 Mar 1;27(3):pyae014.
doi: 10.1093/ijnp/pyae014.

Network Meta-Analysis Indicates Superior Effects of Omega-3 Polyunsaturated Fatty Acids in Preventing the Transition to Psychosis in Individuals at Clinical High-Risk

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Network Meta-Analysis Indicates Superior Effects of Omega-3 Polyunsaturated Fatty Acids in Preventing the Transition to Psychosis in Individuals at Clinical High-Risk

Chengfeng Chen et al. Int J Neuropsychopharmacol. .

Abstract

Background: The efficacy of pharmacological and nutritional interventions in individuals at clinical high risk for psychosis (CHR-P) remains elusive. This study aims to investigate the efficacy of pharmacological and nutritional interventions in CHR-P and whether these interventions can enhance the efficacy of psychological treatments.

Methods: We systematically reviewed data from 5 databases until July 24, 2021: PubMed, Web of Science, EMBASE, China National Knowledge Infrastructure, and WanFang Data. The primary outcome was the transition to psychosis. Network meta-analyses were conducted at 3 time points (6, 12, and ≥24 months) considering both pharmacological/nutritional interventions alone and its combination with psychotherapy.

Results: Out of 11 417 identified references, 21 studies were included, comprising 1983 participants. CHR-P participants receiving omega-3 polyunsaturated fatty acids treatment were associated with a lower probability of transition compared with placebo/control at 6 months (odds ratio [OR] = 0.07, 95% confidence interval [CI] = .01 to .054), 12 months (OR = 0.14, 95% CI = .03 to .66), and ≥24 months (OR = 0.16, 95% CI = .05 to .54). Moreover, risperidone plus psychotherapy was associated with a lower likelihood of transition at 6 months compared with placebo/control plus psychotherapy, but this result was not sustained over longer durations.

Conclusion: Omega-3 polyunsaturated fatty acids helped in preventing transitions to psychosis compared with controls.

Prospero registration number: CRD42021256209.

Keywords: Clinical high risk of psychosis; network meta-analysis; omega-3 polyunsaturated fatty acids.

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Figures

Figure 1.
Figure 1.
PRISMA flow chart of the study selection process.
Figure 2.
Figure 2.
Network plots of direct comparisons in the network meta-analysis for transition outcome at 6, 12, and ≥24 months in 2 levels: pharmacological/nutritional interventions group (on the left) and pharmacological/nutritional interventions plus psychotherapy group (on the right). The width of the lines is proportional to the number of trials comparing each pair of treatments. AD, antidepressants; AP, antipsychotics; ARI, aripiprazole; BEN, benzodiazepine; Dser, D-serine; MS, mood stabilizers; NBI, needs-based interventions; OLA, olanzapine; Omega-3, omega-3 fatty acids; Pharm/Nutr interventions, pharmacological/nutritional interventions; Plcb/Ctrl, placebo/control; PT, psychotherapy; RIS, risperidone; ZIP, ziprasidone.
Figure 3.
Figure 3.
Forest plot of comparison in the risk ratio of conversion to psychosis in the network meta-analysis for transition outcome at 6, 12, and ≥24 months in 2 levels: pharmacological/nutritional interventions group (on the left) and pharmacological/nutritional interventions plus psychotherapy group (on the right). *Bold letters indicate statistical significance. AD, antidepressants; AP, antipsychotics; ARI, aripiprazole; BEN, benzodiazepine; CI, confidence interval; Dser, D-serine; MS, mood stabilizers; NBI, needs-based interventions; OLA, olanzapine; Omega-3, omega-3 fatty acids; OR, odds ratio; Pharm/Nutr interventions, pharmacological/nutritional interventions; Plcb/Ctrl, placebo/control; PT, psychotherapy; RIS, risperidone; ZIP, ziprasidone.

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