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Authors Yang X, Wang G, Wang Y, Yue X
Published Date March 2015 Volume 2015:11 Pages 823—833
DOI http://dx.doi.org/10.2147/NDT.S77966
Received 22 November 2014, Accepted 22 January 2015, Published 25 March 2015
Abstract: To date, the
role of metabotropic glutamate receptor 3 (GRM3) rs274622, rs1468412, rs917071,
rs6465084, and rs2299225 polymorphisms in schizophrenia remains controversial.
To provide a clearer picture for the effect of the five most studied GRM3
polymorphisms on risk of schizophrenia, this meta-analysis with eligible data
from published studies was performed. Relevant case–control studies were
retrieved by literature search and selected according to established inclusion
criteria. Odds ratios with 95% confidence intervals were used to assess the
strength of association. A total of 33 individual studies were identified and
included in our meta-analysis: nine for rs1468412, with 5,314 cases and 6,147
controls; six for rs917071, with 2,660 cases and 3,517 controls; seven for
rs274622, with 3,820 cases and 4,015 controls; five for rs2299225, with 3,492
cases and 3,735 controls; and six for rs6465084, with 4,960 cases and 5,613
controls. However, no significant association was found between these GRM3
polymorphisms and schizophrenia in the overall population. With respect to
rs1468412 polymorphism, a finding of very borderline statistical significance
emerged in dominant comparison model for non-Asian populations, calling for
large-scale verification to assess the marginally elevated risk of
schizophrenia. In conclusion, these GRM3 polymorphisms have limited effect on
the risks of schizophrenia. Further large and well-designed studies are needed
to confirm this conclusion.
Keywords: schizophrenia, GRM3,
SNP, meta-analysis