Low Dietary Folate Interacts with MTHFD1 Synthetase Deficiency in Mice, a Model for the R653Q Variant, to Increase Incidence of Developmental Delays and Defects. Issue 4 (11th April 2018)

• Record Type: Journal Article
• Authors: Christensen, Karen E; Bahous, Renata H; Hou, Wenyang; Deng, Liyuan; Malysheva, Olga V; Arning, Erland; Bottiglieri, Teodoro; Caudill, Marie A; Jerome-Majewska, Loydie A; Rozen, Rima
• Is Part Of: Journal of nutrition. Volume 148:Issue 4(2018)
• Page Start: 501
• Page End: 509
• Publication Date: 2018-04-11
• Subjects: MTHFD1 -- folic acid -- low folate -- developmental delay -- developmental defects -- embryo -- placenta -- birth defects -- S-adenosylmethionine; Nutrition -- Periodicals; Diet -- Periodicals; 613.205
• DOI: 10.1093/jn/nxy013
• Languages: English
• ISSNs: 0022-3166

Abstract

Abstract: Background: Suboptimal folate intake, a risk factor for birth defects, is common even in areas with folate fortification. A polymorphism in methylenetetrahydrofolate dehydrogenase 1 (MTHFD1), R653Q ( MTHFD1 c.1958 G > A ), has also been associated with increased birth defect risk, likely through reduced purine synthesis. Objective: We aimed to determine if the interaction of MTHFD1 synthetase deficiency and low folate intake increases developmental abnormalities in a mouse model for MTHFD1 R653Q. Methods: Female Mthfd1S +/+ and Mthfd1S +/ − mice were fed control or low-folate diets (2 and 0.3 mg folic acid/kg diet, respectively) before mating and during pregnancy. Embryos and placentas were examined for anomalies at embryonic day 10.5. Maternal 1-carbon metabolites were measured in plasma and liver. Results: Delays and defects doubled in litters of Mthfd1S +/ − females fed low-folate diets compared to wild-type females fed either diet, or Mthfd1S +/ − females fed control diets [ P values (defects): diet 0.003, maternal genotype 0.012, diet × maternal genotype 0.014]. These adverse outcomes were associated with placental dysmorphology. Intrauterine growth restriction was increased by embryonic Mthfd1S +/ − genotype, folate deficiency, and interaction of maternal Mthfd1S +/ − genotype with folate deficiency ( P values: embryonic genotype 0.045, diet 0.0081, diet × maternal genotype 0.0019). Despite a 50% increase in methylenetetrahydrofolate reductase expression in low-folate maternal liver ( P diet = 0.0007), methyltetrahydrofolate concentration decreased 70% ( P diet <0.0001) and homocysteine concentration doubled in plasma ( P diet = 0.0001); S -adenosylmethionine decreased 40% and S -adenosylhomocysteine increased 20% in low-folate maternal liver ( P diet = 0.002 and 0.0002, respectively). Conclusions: MTHFD1 synthetase-deficient mice are more sensitive to low folate intake than wild-type mice during pregnancy. Reduced purine synthesis due to synthetase deficiency and altered methylation potential due to low folate may increase pregnancy complications. Further studies and individualized intake recommendations may be required for women homozygous for the MTHFD1 R653Q variant.