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A118G Polymorphism of OPRM1 Gene is Associated with Schizophrenia

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Abstract

Schizophrenia is ranked among multifactor diseases in whose pathogenesis, besides environmental factors, an interplay of functional polymorphisms of a larger number of candidate genes is involved. Neurodevelopmental abnormities are among the most accepted hypotheses in the etiology of schizophrenia. Recently, the role of oligodendrocytes in the development of the cortex has been cited repeatedly. During their various phases of differentiation oligodendrocytes present on their surfaces diverse receptors, among others the μ-opioid receptor (OPRM1). The study was focused on the relationship between the functional A118G polymorphism of the OPRM1 gene (rs1799971) and schizophrenia in groups of 130 male patients and 452 male controls. An association study revealed yet unpublished statistically significant difference of allelic and genotypic frequencies between the control and patient groups. According to our present knowledge, we assume that the OPRM1 gene polymorphism can influence the myelination of CNS neurons through regulations of expression of OPRM1 receptors on surfaces of oligodendrocytes. The neuronal myelination seems to be one of the important factors in the pathogenesis of schizophrenia.

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Abbreviations

CNS:

central nervous system

GABA:

gamma-aminobutyric acid

OPRM1:

opioid receptor, mu 1

PCR:

polymerase chain reaction

SNPs:

single nucleotide polymorphisms

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Acknowledgments

This project was supported by the Internal Grant Agency of the Ministry of Health of the Czech Republic—IGA MZ CR Nr. NR9298-3/2007 and by a project of the Ministry of Education, Youth and Sports of the Czech Republic Nr. MSM0021622413.

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Correspondence to Omar Šerý.

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Šerý, O., Přikryl, R., Častulík, L. et al. A118G Polymorphism of OPRM1 Gene is Associated with Schizophrenia. J Mol Neurosci 41, 219–222 (2010). https://doi.org/10.1007/s12031-010-9327-z

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  • DOI: https://doi.org/10.1007/s12031-010-9327-z

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