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

被引:76
|
作者
Lewis, SJ
Zammit, S
Gunnell, D
Smith, GD
机构
[1] Univ Bristol, Dept Social Med, Bristol BS8 2PR, Avon, England
[2] Univ Wales Coll Cardiff, Coll Med, Dept Psychol Med, Cardiff CF1 3NS, S Glam, Wales
基金
英国医学研究理事会;
关键词
MTHFR; schizophrenia; folate; polymorphism;
D O I
10.1002/ajmg.b.30170
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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. (c) 2005 Wiley-Liss, Inc.
引用
收藏
页码:2 / 4
页数:3
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