Journal article
Association between type-three metabotropic glutamate receptor gene (GRM3) variants and symptom presentation in treatment refractory schizophrenia
Human psychopharmacology, Vol.26(1), pp.28-34
01/2011
DOI: 10.1002/hup.1163
PMCID: PMC3199025
PMID: 21344500
Abstract
Positive associations between polymorphisms in the type-three metabotropic glutamate receptor gene (GRM3) and the pathogenesis of schizophrenia as well as response to antipsychotic treatment have been reported. The objective of this study was to determine whether refractory psychiatric symptoms in antipsychotic non-responders are related to polymorphisms in GRM3.
Ninety-five treatment refractory schizophrenia participants were enrolled. Prior to a medication switch, global psychopathology and negative symptoms were rated. These participants were genotyped for seven markers in GRM3. Genotype associations with symptoms were assessed.
Two markers in GRM3 (rs1989796 and rs1476455), were associated with the presence of refractory global symptoms as measured by the Brief Psychiatric Rating Scale (BPRS) Total scores. Participants with an rs1476455_CC genotype had significantly higher BPRS scores than A-carriers (55.1±10.4 vs. 48.3±9.2; F=7.6, p=0.0071). Additionally, participants with the rs1989796_CC genotype had significantly higher BPRS scores than T-carriers (50.1±5.7 vs. 55.8±10.5, F=7.1, p=0.0091). No evidence for significant associations with negative symptoms was observed.
Polymorphisms in the GRM3 gene may be associated with refractory global psychosis symptoms but not negative symptoms in persons with schizophrenia.
Details
- Title: Subtitle
- Association between type-three metabotropic glutamate receptor gene (GRM3) variants and symptom presentation in treatment refractory schizophrenia
- Creators
- Jeffrey R Bishop - Department of Pharmacy Practice, University of Illinois at Chicago College of Pharmacy, Chicago, Illinois 60612, USA. jbishop@uic.eduDel D MillerVicki L EllingrodTimothy Holman
- Resource Type
- Journal article
- Publication Details
- Human psychopharmacology, Vol.26(1), pp.28-34
- Publisher
- England
- DOI
- 10.1002/hup.1163
- PMID
- 21344500
- PMCID
- PMC3199025
- ISSN
- 0885-6222
- eISSN
- 1099-1077
- Grant note
- K23 MH001758-05 / NIMH NIH HHS K08MH083888 / NIMH NIH HHS R01 MH082784 / NIMH NIH HHS K23 MH001758 / NIMH NIH HHS K08 MH083888 / NIMH NIH HHS K08 MH064158 / NIMH NIH HHS K08MH64158 / NIMH NIH HHS K23MH01758 / NIMH NIH HHS M01-RR-59 / NCRR NIH HHS K08 MH064158-05 / NIMH NIH HHS K08 MH083888-01A1 / NIMH NIH HHS
- Language
- English
- Date published
- 01/2011
- Academic Unit
- Psychiatry
- Record Identifier
- 9984003458102771
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