Literature DB >> 15895286

Assessment of tailor-made prevention of atherosclerosis with folic acid supplementation: randomized, double-blind, placebo-controlled trials in each MTHFR C677T genotype.

Koichi Miyaki1, Mitsuru Murata2,3, Haruhito Kikuchi3, Izumi Takei2,3, Takeo Nakayama4, Kiyoaki Watanabe3, Kazuyuki Omae5.   

Abstract

This study aimed at assessing the effect of folic acid supplementation quantitatively in each MTHFR C677T genotype and considered the efficiency of tailor-made prevention of atherosclerosis. Study design was genotype-stratified, randomized, double-blind, placebo-controlled trials. The setting was a Japanese company in the chemical industry. Subjects were 203 healthy men after exclusion of those who took folic acid or drugs known to effect folic acid metabolism. Intervention was folic acid 1 mg/day p.o. for 3 months. The primary endpoint was plasma total homocysteine level (tHcy). In all three genotypes, there were significant tHcy decreases. The greatest decrease was in the TT homozygote [6.61 (3.47-9.76) micromol/l] compared with other genotypes [CC: 2.59 (1.81-3.36), CT: 2.64 (2.16-3.13)], and there was a significant trend between the mutated allele number and the decrease. The tHcy were significantly lowered in all the genotypes, but the amount of the decrease differed significantly in each genotype, which was observed at both 1 and 3 months. Using these time-series data, the largest benefit obtained by the TT homozygote was appraised as 2.4 times compared with the CC homozygote. Taking into account the high allele frequency of this SNP, this quantitative assessment should be useful when considering tailor-made prevention of atherosclerosis with folic acid.

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Year:  2005        PMID: 15895286     DOI: 10.1007/s10038-005-0247-7

Source DB:  PubMed          Journal:  J Hum Genet        ISSN: 1434-5161            Impact factor:   3.172


  29 in total

1.  The CONSORT statement: revised recommendations for improving the quality of reports of parallel-group randomised trials.

Authors:  D Moher; K F Schulz; D G Altman
Journal:  Lancet       Date:  2001-04-14       Impact factor: 79.321

2.  MTHFR 677C-->T polymorphism and risk of coronary heart disease: a meta-analysis.

Authors:  Mariska Klerk; Petra Verhoef; Robert Clarke; Henk J Blom; Frans J Kok; Evert G Schouten
Journal:  JAMA       Date:  2002 Oct 23-30       Impact factor: 56.272

3.  Randomized trial of folic acid supplementation and serum homocysteine levels.

Authors:  D S Wald; L Bishop; N J Wald; M Law; E Hennessy; D Weir; J McPartlin; J Scott
Journal:  Arch Intern Med       Date:  2001-03-12

4.  Folic acid enhances endothelial function and reduces blood pressure in smokers: a randomized controlled trial.

Authors:  A A Mangoni; R A Sherwood; C G Swift; S H D Jackson
Journal:  J Intern Med       Date:  2002-12       Impact factor: 8.989

5.  The structure and properties of methylenetetrahydrofolate reductase from Escherichia coli suggest how folate ameliorates human hyperhomocysteinemia.

Authors:  B D Guenther; C A Sheppard; P Tran; R Rozen; R G Matthews; M L Ludwig
Journal:  Nat Struct Biol       Date:  1999-04

Review 6.  Homocysteine and vascular disease.

Authors:  G J Hankey; J W Eikelboom
Journal:  Lancet       Date:  1999-07-31       Impact factor: 79.321

7.  The effect of folic acid fortification on plasma folate and total homocysteine concentrations.

Authors:  P F Jacques; J Selhub; A G Bostom; P W Wilson; I H Rosenberg
Journal:  N Engl J Med       Date:  1999-05-13       Impact factor: 91.245

8.  Dietary counseling to increase natural folate intake: a randomized, placebo-controlled trial in free-living subjects to assess effects on serum folate and plasma total homocysteine.

Authors:  Bernard J Venn; Jim I Mann; Sheila M Williams; Lynnette J Riddell; Alexandra Chisholm; Michelle J Harper; Wendy Aitken
Journal:  Am J Clin Nutr       Date:  2002-10       Impact factor: 7.045

9.  Homocysteine and cardiovascular disease: evidence on causality from a meta-analysis.

Authors:  David S Wald; Malcolm Law; Joan K Morris
Journal:  BMJ       Date:  2002-11-23

10.  A quantitative assessment of plasma homocysteine as a risk factor for vascular disease. Probable benefits of increasing folic acid intakes.

Authors:  C J Boushey; S A Beresford; G S Omenn; A G Motulsky
Journal:  JAMA       Date:  1995-10-04       Impact factor: 56.272

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  5 in total

1.  The impact of MTHFR 677 C/T genotypes on folate status markers: a meta-analysis of folic acid intervention studies.

Authors:  Natalie J Colson; Helen L Naug; Elham Nikbakht; Ping Zhang; Joanna McCormack
Journal:  Eur J Nutr       Date:  2015-10-23       Impact factor: 5.614

Review 2.  Genetic polymorphisms in homocysteine metabolism and response to folate intake: a comprehensive strategy to elucidate useful genetic information.

Authors:  Koichi Miyaki
Journal:  J Epidemiol       Date:  2010-06-19       Impact factor: 3.211

3.  Increasing the number of SNP loci does not necessarily improve prediction power at least in the comparison of MTHFR SNP and haplotypes.

Authors:  Koichi Miyaki; Yoshimitsu Takahashi; Yixuan Song; Ling Zhang; Masaaki Muramatsu; Takeo Nakayama
Journal:  J Epidemiol       Date:  2008-12-09       Impact factor: 3.211

4.  Serum folate and methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism adjusted for folate intake.

Authors:  Kazuko Nishio; Yasuyuki Goto; Takaaki Kondo; Shimon Ito; Yoshiko Ishida; Sayo Kawai; Mariko Naito; Kenji Wakai; Nobuyuki Hamajima
Journal:  J Epidemiol       Date:  2008-05-14       Impact factor: 3.211

5.  The Effect of Interactions between Folic Acid Supplementation and One Carbon Metabolism Gene Variants on Small-for-Gestational-Age Births in the Screening for Pregnancy Endpoints (SCOPE) Cohort Study.

Authors:  Rhodi E Bulloch; Clare R Wall; Lesley M E McCowan; Rennae S Taylor; Claire T Roberts; John M D Thompson
Journal:  Nutrients       Date:  2020-06-04       Impact factor: 5.717

  5 in total

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