• Title of article

    Red blood cell folate vitamer distribution in healthy subjects is determined by the methylenetetrahydrofolate reductase C677T polymorphism and by the total folate status

  • Author/Authors

    Yvo M. Smulders، نويسنده , , Desiree E.C. Smith، نويسنده , , Robert M. Kok، نويسنده , , Tom Teerlink، نويسنده , , Henkjan Gellekink، نويسنده , , Wouter H.J. Vaes، نويسنده , , Coen DA Stehouwer، نويسنده , , Cornelis Jakobs، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2007
  • Pages
    7
  • From page
    693
  • To page
    699
  • Abstract
    Background Red blood cells (RBCs) represent a storage pool for folate. In contrast to plasma, RBC folate can appear in different biochemical isoforms. So far, only the methylenetetrahydrofolate reductase (MTHFR) 677 TT genotype has been identified as a determinant of RBC folate vitamer distribution. Objective The purpose of this study is to identify clinical and biochemical determinants of RBC folate vitamer distribution in healthy subjects. Design In an observational study, 109 subjects, aged 18 to 65 years, were studied. Red blood cell folate vitamers were analyzed using a liquid chromatography–tandem mass spectrometry method. Other variables recorded included vitamin B2, B6 and B12 status, homocysteine, plasma and RBC S-adenosylhomocysteine and S-adenosylmethionine, renal function and the MTHFR C677T polymorphism. Results The MTHFR C677T genotype was the dominant determinant of nonmethylfolate accumulation. The median (range) nonmethylfolate/total folate ratio was 0.58% (0–12.2%) in the MTHFR CC group (n=55), 0.99% (0–14.3%) in the CT group (n=39) and 30.3% (5.7–73.3%) in the TT genotype group (n=15), P<.001. The 95th percentile for the nonmethylfolate/total folate ratio was 2.8% for the CC group, 9.1% for the CT group and 73.3% for the TT group. In the CC and CT genotype subjects, the T-allele and total folate status were positively and independently correlated with nonmethylfolate accumulation, but the degree of nonmethylfolate accumulation in these subjects was usually minor compared with those with the TT genotype. None of the other studied variables was associated with nonmethylfolate accumulation. Conclusions The MTHFR C677T genotype is the dominant determinant of nonmethylfolate accumulation in RBCs. In addition, high total folate status may contribute to minor to moderate nonmethylfolate accumulation in MTHFR CC and CT subjects. Citing articles (21) Not entitled to full text Calendar
  • Keywords
    Folate , Methylenetetrahydrofolate reductase (MTHFR) , B Vitamins , mass spectrometry , Red blood cell
  • Journal title
    The Journal of Nutritional Biochemistry
  • Serial Year
    2007
  • Journal title
    The Journal of Nutritional Biochemistry
  • Record number

    1299352