Polymorphisms of Genes Involved in the Folate Metabolic Pathway Impact the Occurrence of Unexplained Recurrent Pregnancy Loss. (July 2015)

• Record Type: Journal Article
• Authors: Luo, Li; Chen, Yueming; Wang, Li; Zhuo, Guangchao; Qiu, Chunning; Tu, Qiaofeng; Mei, Jin; Zhang, Wen; Qian, Xia; Wang, Xianjun
• Is Part Of: Reproductive sciences. Volume 22:Number 7(2015:Jul.)
• Page Start: 845
• Page End: 851
• Publication Date: 2015-07
• Subjects: folate metabolism -- unexplained recurrent pregnancy loss -- gene polymorphism -- haplotype; Reproductive health -- Periodicals; Reproduction -- Periodicals; 612.6
• DOI: 10.1177/1933719114565033
• Languages: English
• ISSNs: 1933-7191

Abstract

Low levels of folate combined with high levels of homocysteine may cause unexplained recurrent pregnancy loss (URPL). However, the relationships between polymorphisms in genes of the folate metabolic pathway and URPL remain controversial. We conducted a case-control study to explore polymorphisms of the major folate pathway genes, including methylenetetrahydrofolate reductase (MTHFR) 677C>T, MTHFR 1298A>C, methionine synthase (MTR) 2756A>G, methionine synthase reductase (MTRR) 66A>G and reduced folate carrier 1 (RFC-1) 80A>G, and their associations with URPL. Polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) was used to determine the distributions of MTHFR, MTR and RFC-1 polymorphisms, and the results were validated using direct sequencing. The polymorphisms in MTRR were determined using direct sequencing. Haplotypes were analyzed using SHEsis, an online tool for biological analysis. We found that the MTHFR 677T allele and the 677T/1298A/2756A/66A/80G haplotype were risk factors for URPL, while the MTR 2756G allele and the 677C/1298A/2756A/66A/80A haplotype exhibited protective effects on susceptibility to URPL in a Chinese Han population from the Hangzhou area.