Copyright © 2007 The American Society of Human Genetics. All rights reserved.
The American Journal of Human Genetics, Volume 80, Issue 5, 846-855, 1 May 2007
doi:10.1086/513520
Article
Steinar Hustada,
,
, Øivind Midttun, Jørn Schneede, Stein Emil Vollset, Tom Grotmole and Per Magne Uelandc
a From The Hormone Laboratory, Haukeland University Hospital University of Bergen, and Bevital AS Bergen, Norway
b LOCUS for Homocysteine and Related Vitamins University of Bergen, and Bevital AS Bergen, Norway
c Section for Pharmacology, Institute of Medicine University of Bergen, and Bevital AS Bergen, Norway
d The Cancer Registry of Norway, Oslo (T.G.)
Address for correspondence and reprints: Dr. Steinar Hustad, The Hormone Laboratory, Haukeland University Hospital, 5021 Bergen, Norway.Abstract
Folates are carriers of one-carbon units and are metabolized by 5,10-methylenetetrahydrofolate reductase (MTHFR) and other enzymes that use riboflavin, cobalamin, or vitamin B6 as cofactors. These B vitamins are essential for the remethylation and transsulfuration of homocysteine, which is an important intermediate in one-carbon metabolism. We studied the MTHFR 677C→T polymorphism and B vitamins as modulators of one-carbon metabolism in 10,601 adults from the Norwegian Colorectal Cancer Prevention (NORCCAP) cohort, using plasma total homocysteine (tHcy) as the main outcome measure. Mean concentrations of plasma tHcy were 10.4 μmol/liter, 10.9 μmol/liter, and 13.3 μmol/liter in subjects with the CC (51%), CT (41%), and TT (8%) genotypes, respectively. The MTHFR 677C→T polymorphism, folate, riboflavin, cobalamin, and vitamin B6 were independent predictors of tHcy in multivariate models (P<.001), and genotype effects were strongest when B vitamins were low (P≤.006). Conversely, the MTHFR polymorphism influenced B vitamin effects, which were strongest in the TT group, in which the estimated tHcy difference between subjects with vitamin concentrations in the lowest compared with the highest quartile was 5.4 μmol/liter for folate, 4.1 μmol/liter for riboflavin, 3.2 μmol/liter for cobalamin, and 2.1 μmol/liter for vitamin B6. Furthermore, interactions between B vitamins were observed, and B vitamins were more strongly related to plasma tHcy when concentrations of other B vitamins were low. The study provides comprehensive data on the MTHFR–B vitamin network, which has major effects on the transfer of one-carbon units. Individuals with the TT genotype were particularly sensitive to the status of several B vitamins and might be candidates for personalized nutritional recommendations.
| Measurement and Use of Total Plasma Homocysteine The American Journal of Human Genetics, Volume 63, Issue 5, 1 November 1998, Pages 1541-1543 Abstract Summary:
Hyperhomocysteinemia, which is a recognized independent risk factor for premature vascular occlusion, is defined as a fasting total plasma homocysteine (tHcy) level >15 μM. There may also be graded increased risks for persons with tHcy concentrations of 10–15 μM. The measurement of tHcy requires precise sample collection, immediate separation and freezing of plasma, and referral to a specialized laboratory. The etiologies of hyperhomocysteinemia are complex and involve both genetic and environmental factors. Because the inappropriate supplementation of involved cofactors can be harmful, it is important to identify the cause of hyperhomocysteinemia prior to treatment. Abstract | | |
| Neonatal and Fetal Methylenetetrahydrofolate Reductase Genetic Polymorphisms: An Examination of C677T and A1298C Mutations The American Journal of Human Genetics, Volume 67, Issue 4, 1 October 2000, Pages 986-990 Phillip A. Isotalo, George A. Wells and James G. Donnelly Abstract Methylenetetrahydrofolate reductase (MTHFR) mutations are commonly associated with hyperhomocysteinemia, and, through their defects in homocysteine metabolism, they have been implicated as risk factors for neural tube defects and unexplained, recurrent embryo losses in early pregnancy. Folate sufficiency is thought to play an integral role in the phenotypic expression of MTHFR mutations. Samples of neonatal cord blood (n=119) and fetal tissue (n=161) were analyzed for MTHFR C677T and A1298C mutations to determine whether certain MTHFR genotype combinations were associated with decreased in utero viability. Mutation analysis revealed that all possible MTHFR genotype combinations were represented in the fetal group, demonstrating that 677T and 1298C alleles could occur in both cis and trans configurations. Combined 677CT/1298CC and 677TT/1298CC genotypes, which contain three and four mutant alleles, respectively, were not observed in the neonatal group (P=.0402). This suggests decreased viability among fetuses carrying these mutations and a possible selection disadvantage among fetuses with increased numbers of mutant MTHFR alleles. This is the first report that describes the existence of human MTHFR 677CT/1298CC and 677TT/1298CC genotypes and demonstrates their potential role in compromised fetal viability. Abstract | | |
| A Second Common Mutation in the Methylenetetrahydrofolate Reductase Gene: An Additional Risk Factor for Neural-Tube Defects? The American Journal of Human Genetics, Volume 62, Issue 5, 1 May 1998, Pages 1044-1051 Nathalie M.J. van der Put, Fons Gabreëls, Erik M.B. Stevens, Jan A.M. Smeitink, Frans J.M. Trijbels, Tom K.A.B. Eskes, Lambert P. van den Heuvel and Henk J. Blom Abstract Summary:
Recently, we showed that homozygosity for the common 677(C→T) mutation in the methylenetetrahydrofolate reductase (MTHFR) gene, causing thermolability of the enzyme, is a risk factor for neural-tube defects (NTDs). We now report on another mutation in the same gene, the 1298(A→C) mutation, which changes a glutamate into an alanine residue. This mutation destroys an MboII recognition site and has an allele frequency of .33. This 1298(A→C) mutation results in decreased MTHFR activity (one-way analysis of variance [ANOVA] P<.0001), which is more pronounced in the homozygous than heterozygous state. Neither the homozygous nor the heterozygous state is associated with higher plasma homocysteine (Hcy) or a lower plasma folate concentration—phenomena that are evident with homozygosity for the 677(C→T) mutation. However, there appears to be an interaction between these two common mutations. When compared with heterozygosity for either the 677(C→T) or 1298(A→C) mutations, the combined heterozygosity for the 1298(A→C) and 677(C→T) mutations was associated with reduced MTHFR specific activity (ANOVA P <.0001), higher Hcy, and decreased plasma folate levels (ANOVA P<.03). Thus, combined heterozygosity for both MTHFR mutations results in similar features as observed in homozygotes for the 677(C→T) mutation. This combined heterozygosity was observed in 28% (n = 86) of the NTD patients compared with 20% (n = 403) among controls, resulting in an odds ratio of 2.04 (95% confidence interval: .9–4.7). These data suggest that the combined heterozygosity for the two MTHFR common mutations accounts for a proportion of folate-related NTDs, which is not explained by homozygosity for the 677(C→T) mutation, and can be an additional genetic risk factor for NTDs. Abstract | | |