Association Between Methionine Synthase Reductase A66G Polymorphism and the Risk of Congenital Heart Defects: Evidence From Eight Case-Control Studies

作者：Yu Di; Yang Lei; Shen Shutong; Fan Changfeng; Zhang Weiyan; Mo Xuming^*

来源：Pediatric Cardiology, 2014, 35(7): 1091-1098.

DOI：10.1007/s00246-014-0948-9

• Methionine synthase reductase
• Polymorphism
• Congenital heart defects
• Metaanalysis

Methionine synthase reductase (MTRR) plays a major role in hyperhomocysteinemia, a risk factor related to the occurrence of congenital heart defects (CHDs). However, the associations between MTRR polymorphism and CHDs have been inconclusive. Thus, a metaanalysis of eight case-control studies was conducted to investigate 3,592 cases and 3,638 control subjects for MTRR A66G polymorphism to identify the association. Odds ratios (ORs) and 95 % confidence intervals (95 % CIs) were used to assess the strength of the association. The results showed that MTRR A66G polymorphism was associated with a higher CHD risk in the allele comparison (G vs A: OR 1.163; 95 % CI 1.016-1.330; P (heterogeneity) = 0.004), the homozygote comparison (GG vs AA: OR 1.332; 95 % CI 1.020-1.740; P (heterogeneity) = 0.035), and the dominant model (GG/AG vs AA: OR 1.218; 95 % CI 1.001-1.482; P (heterogeneity) = 0.001). In the subgroup analysis, this polymorphism was associated with CHDs in Asians in the homozygote comparison (GG vs AA: OR 1.427; 95 % CI 1.017-2.001; P (heterogeneity) = 0.019) and the allele comparison (G vs A: OR 1.203; 95 % CI 1.018-1.422; P (heterogeneity) = 0.002). In summary, the metaanalysis demonstrated that MTRR A66G polymorphism is a risk factor for CHDs. Further studies should be performed to investigate the association of plasma homocysteine levels, enzyme activity, parental genotypes, and vitamin complex intakes with the risk of CHDs.

• 出版日期2014-10
• 单位南京医科大学