Abstract

The influence of CYP enzymes and ABCB1 on treatment outcomes in schizophrenia: association of CYP1A2 activity with adverse effects

Highlights

  • Antipsychotic drugs are the mainstay of treatment for severe mental disorders such as schizophrenia and bipolar disorders

  • CYP1A2 was found to be associated with psychic side effects (P = 0.02), with variants predicting higher enzyme activity associated with lower adverse effects, and was the strongest predictor for this adverse effect of all the studied factors

  • Functional variants in CYP genes were associated with plasma level differences, with higher activity variants associated with lower plasma levels

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Summary

Introduction

Antipsychotic drugs are the mainstay of treatment for severe mental disorders such as schizophrenia and bipolar disorders. Plasma levels and all processes capable of affecting them may modify the dose-dependent fraction of the drug’s response These processes include transport across biological membranes, such as absorption and excretion, and metabolism. Individuals with greater metabolism may require higher doses, while those with lower metabolic rates might be more prone to the drugs’ adverse effects and need dose reduction[3,4,5,6,7]. With all these variables potential predictors of drug response, which of them, or combination of, is the best predictor of clinical endpoints, if at all

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