Abstract

Antipsychotic effects seem to decrease in relapsed schizophrenia patients and the underlying mechanisms remain to be elucidated. Based on the essential role of polyunsaturated fatty acids in brain function and the treatment of schizophrenia, we hypothesize that disordered fatty acid metabolism may contribute to treatment resistance in multi-episode patients. We analyzed the erythrocyte membrane fatty acids in 327 schizophrenia patients under various episodes (numbers of patients: first-episode drug naïve 89; 2–3 episodes 110; 4–6 episodes 80; over 6 episodes 48) and 159 age- and gender-matched healthy controls. Membrane fatty acid levels and PANSS scales were assessed at baseline of antipsychotic-free period and one-month of follow-up after treatment. Totally, both saturated and unsaturated fatty acids were reduced at baseline when compared to healthy controls. Subgroup analyses among different episodes indicated that in response to atypical antipsychotic treatment, the membrane fatty acids were only increased in patients within 3 episodes, and this therapeutic effects on omega-3 index were merely present in the first episode. Results of fatty acid ratios suggested that dysregulations of enzymes such as D6 desaturase, D5 desaturase, and elongases for polyunsaturated fatty acids in patients with multi-episode schizophrenia could account for the differences. Additionally, certain fatty acid level/ratio changes were positively correlated with symptom improvement. The alterations of C22:5n3 and omega-3 index, gender, and the number of episodes were significant risk factors correlated with treatment responsiveness. Using targeted metabolomic approach, we revealed the potential mechanisms underlying abnormal fatty acid metabolism responsible for reduced treatment response in patients with multi-episode schizophrenia.

Highlights

  • Antipsychotic maintenance treatment is critically important for the prevention of relapse in schizophrenia[1]

  • A cohort of 327 patients with schizophrenia and 159 healthy controls from 2016 to 2018 was recruited and the characteristics of the subjects are presented in Supplementary Table 1

  • Half of the patients were treated with risperidone or olanzapine, while 30% of the patients received combination treatment with atypical antipsychotic drugs (AAPDs)

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Summary

Introduction

Antipsychotic maintenance treatment is critically important for the prevention of relapse in schizophrenia[1]. Poor compliance in patients with schizophrenia results in a high risk of relapse[2]. Antipsychotic treatment response is reported to be diminished in the second episode compared with the first episode during the follow-up of the same group of patients[3]. The problem of antipsychotic treatment resistance in subsequent psychotic episodes has been discussed but the underlying mechanisms remain unclear[4]. Dopaminergic neurotransmission interacts with membrane phospholipids in cognitive deficits of schizophrenia[7]. A lipidomic analysis has suggested that changes in specific lipid profiles are associated with poor or good response to atypical antipsychotic treatment in schizophrenia[9]. It is critical to explore the role of membrane phospholipids in the treatment resistance of patients with multiepisode schizophrenia

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