Human Genetics

, Volume 121, Issue 1, pp 57–64 | Cite as

Functional inference of the methylenetetrahydrofolate reductase 677 C > T and 1298A > C polymorphisms from a large-scale epidemiological study

  • Arve Ulvik
  • Per M. Ueland
  • Åse Fredriksen
  • Klaus Meyer
  • Stein Emil Vollset
  • Geir Hoff
  • Jørn Schneede
Original Investigation

Abstract

Two functional single nucleotide polymorphisms, 677C > T and 1298A > C have been described for the methylenetetrahydrofolate (MTHFR) gene. Both are associated with reduced enzyme activity in vitro. For the 677T, but not the 1298C allele, significantly lower serum folate and higher plasma total homocysteine (tHcy) have been reported. We genotyped 10,034 middle-aged (50–64 years old) subjects and measured serum folate and tHcy. Within strata of 677 genotypes, 1,298 genotypes had significantly different serum folate and tHcy (P ≤ 0.03 for all comparisons). Each additional 1298C allele reduced mean serum folate and increased mean tHcy, by (on average) 4.5 and 3.0%, respectively. In comparison, within strata of 1,298 genotypes, the increase from no, to one 677T-allele reduced serum folate and increased tHcy by, 7.1 and 6.3%, respectively. Lowest serum folate and highest tHcy level was found for the 677TT/1298AA genotype. The difference in tHcy was significantly larger at low folate than at high folate when genotypes 677TT/1298AA and 677CT/1298AA, 677CT/1298AC and 677CC/1298AC, and genotypes 677CT/1298AC and 677CT/1298AA were compared. We interpreted these data in the context of a model of the MTHFR enzyme that describes the enzyme as a dimer that mainly exist in six different configurations. The model reconciled the observed phenotypic effects of the 677/1,298 combination genotypes with previous in vitro measurements, and identified enzyme configurations that are sensitive to low folate levels. In conclusion, this report demonstrates functional inference of the MTHFR 677 C > T and 1,298 A > C polymorphisms from a large-scale epidemiological study.

Notes

Acknowledgments

This study received financial support from the Norwegian Cancer Society, the Norwegian Department of Health and Social Affairs, and the Foundation to Promote Research into Functional Vitamin B12-deficiency.

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Copyright information

© Springer-Verlag 2006

Authors and Affiliations

  • Arve Ulvik
    • 1
  • Per M. Ueland
    • 1
  • Åse Fredriksen
    • 1
  • Klaus Meyer
    • 1
  • Stein Emil Vollset
    • 1
  • Geir Hoff
    • 2
  • Jørn Schneede
    • 1
  1. 1.LOCUS for Homocysteine and Related Vitamins, Department of Internal Medicine, Pharmacology Section University of BergenBergenNorway
  2. 2.The Cancer Registry of NorwayOsloNorway

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