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

Am J Med Genet B Neuropsychiatr Genet. 2005 May 5;135B(1):2-4. doi: 10.1002/ajmg.b.30170.

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.

Publication types

  • Meta-Analysis

MeSH terms

  • Alleles
  • Female
  • Gene Frequency
  • Genotype
  • Humans
  • Male
  • Methylenetetrahydrofolate Reductase (NADPH2) / genetics*
  • Polymorphism, Genetic*
  • Risk Factors
  • Schizophrenia / enzymology
  • Schizophrenia / genetics*

Substances

  • Methylenetetrahydrofolate Reductase (NADPH2)