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Genetic association analysis of N‐methyl‐ d ‐aspartate receptor subunit gene GRIN2B and clinical response to clozapine
Author(s) -
Taylor Danielle L.,
Tiwari Arun K.,
Lieberman Jeffrey A.,
Potkin Steven G.,
Meltzer Herbert Y.,
Knight Jo,
Remington Gary,
Müller Daniel J.,
Kennedy James L.
Publication year - 2016
Publication title -
human psychopharmacology: clinical and experimental
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.461
H-Index - 78
eISSN - 1099-1077
pISSN - 0885-6222
DOI - 10.1002/hup.2519
Subject(s) - clozapine , schizophrenia (object oriented programming) , glutamate receptor , atypical antipsychotic , medicine , antipsychotic , pharmacology , receptor , psychiatry
Objective Approximately 30% of patients with schizophrenia fail to respond to antipsychotic therapy and are classified as having treatment‐resistant schizophrenia. Clozapine is the most efficacious drug for treatment‐resistant schizophrenia and may deliver superior therapeutic effects partly by modulating glutamate neurotransmission. Response to clozapine is highly variable and may depend on genetic factors as indicated by twin studies. We investigated eight polymorphisms in the N‐methyl‐ d ‐aspartate glutamate receptor subunit gene GRIN2B with response to clozapine. Methods GRIN2B variants were genotyped using standard TaqMan procedures in 175 European patients with schizophrenia deemed resistant or intolerant to treatment. Response was assessed using change in Brief Psychiatric Rating Scale scores following six months of clozapine therapy. Categorical and continuous response was assessed using chi‐squared test and analysis of covariance, respectively. Results No associations were observed between the variants and response to clozapine. A‐allele carriers of rs1072388 responded marginally better to clozapine therapy than GG‐homozygotes; however, the difference was not statistically significant ( p = 0.067, uncorrected). Conclusions Our findings do not support a role for these GRIN2B variants in altering response to clozapine in our sample. Investigation of additional glutamate variants in clozapine response is warranted. Copyright © 2016 John Wiley & Sons, Ltd.