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- W2097965819 endingPage "1443" @default.
- W2097965819 startingPage "1437" @default.
- W2097965819 abstract "Aims: Abnormalities in dopaminergic and serotonergic transmission systems are thought to be involved in the pathophysiology of schizophrenia and the mechanisms underlying the therapeutic effects of antipsychotics. We conducted a pharmacogenetic study to evaluate whether variants in dopamine-related genes (DRD1–DRD5, AKT1 and GSK3β) and serotonin receptor genes (HTR1A, HTR1B, HTR1D, HTR2A, HTR2C, HTR6 and HTR7) can be used to predict the efficacy of risperidone treatment for schizophrenia. Materials & methods: A total of 120 first-episode neuroleptic-naive schizophrenia patients were treated with risperidone monotherapy for 8 weeks and clinical symptoms were evaluated by the Positive and Negative Syndrome Scale. Results: Among the 30 variants that we examined, two SNPs in DRD2 (-241A>G [rs1799978] and TaqIA [rs1800497]) and two SNPs in AKT1 (AKT1-SNP1 [rs3803300] and AKT1-SNP5 [rs2494732]) were significant predictors of treatment response to risperidone. Conclusion: These data suggest that the SNPs in DRD2 and AKT1 may influence the treatment response to risperidone in schizophrenia patients." @default.
- W2097965819 created "2016-06-24" @default.
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- W2097965819 date "2008-10-01" @default.
- W2097965819 modified "2023-09-26" @default.
- W2097965819 title "Variants of dopamine and serotonin candidate genes as predictors of response to risperidone treatment in first-episode schizophrenia" @default.
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- W2097965819 doi "https://doi.org/10.2217/14622416.9.10.1437" @default.
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