Literature DB >> 15729744

A meta-analysis of the MTHFR C677T polymorphism and schizophrenia risk.

Sarah J Lewis1, Stanley Zammit, David Gunnell, George Davey Smith.   

Abstract

Epigenetic mechanisms such as methylation of DNA, could lead to abnormal neurodevelopment and may be important in the etiology of schizophrenia. Maternal dietary folate intake may play a role in determining methylation levels. The MTHFR gene C677T polymorphism influences folate metabolism and intracellular availability of folate metabolites for methylation. We carried out a meta-analysis of MTHFR C677T genotype and schizophrenia risk, and found that TT homozygotes had a significantly increased risk, OR 1.48 (1.18-1.86). This supports the hypothesis that folate status is a determinant of schizophrenia risk. Larger studies of this issue are required, together with studies of maternal genotype which could identify whether maternal folate status during pregnancy is important. Copyright 2005 Wiley-Liss, Inc.

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Year:  2005        PMID: 15729744     DOI: 10.1002/ajmg.b.30170

Source DB:  PubMed          Journal:  Am J Med Genet B Neuropsychiatr Genet        ISSN: 1552-4841            Impact factor:   3.568


  24 in total

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Review 2.  Schizophrenia and neural tube defects: comparisons from an epidemiological perspective.

Authors:  Stanley Zammit; Sarah Lewis; David Gunnell; George Davey Smith
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3.  Age Matters: an Atypical Association Between Polymorphism of MTHFR and Clinical Phenotypes in Children with Schizophrenia.

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Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2017-04-24       Impact factor: 3.568

6.  Perinatal folate-related exposures and risk of psychotic symptoms in the ALSPAC birth cohort.

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7.  Association of MTHFR C677T polymorphism with schizophrenia and its effect on episodic memory and gray matter density in patients.

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Review 10.  Genetics and Epigenetics of One-Carbon Metabolism Pathway in Autism Spectrum Disorder: A Sex-Specific Brain Epigenome?

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