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Failure to confirm influence of Methyltetrahydrofolate reductase (MTHFR) polymorphisms on age at onset of Huntington disease
© Hansen et al; licensee BioMed Central Ltd. 2005
Received: 24 May 2005
Accepted: 22 December 2005
Published: 22 December 2005
Huntington disease (HD) is a fully penetrant, autosomal dominantly inherited disorder associated with abnormal expansions of a stretch of perfect CAG repeats in the 5' part of the IT15 gene. The number of repeat units is highly predictive for the age at onset (AO) of the disorder. But AO is only modestly correlated with repeat length when intermediate HD expansions are considered. Recently, suggestive association has been reported between a single nucleotide polymorphism (SNP; rs1801131, also known as A1298C) in the methyltetrahydrofolate reductase (MTHFR) gene and AO of HD. 5,10-MTHFR is a key enzyme in the folate metabolism, diverting metabolites toward methylation reactions or nucleotide synthesis. Using part of a previously established study cohort plus additional patients and appropriate statistical methods, we reinvestigated two polymorphisms in the MTHFR gene, C677T and A1298C, as well as their association with AO in 167 HD patients.
There was no statistically significant impact on AO for HD patients, neither of MTHFR SNPs nor of the combinations thereof.
Contrary to previously described evidence the A1298C polymorphism in the MTHFR gene does not appear to modulate AO of HD patients.
Huntington disease (HD) is caused by expansion of a cytosine-adenine-guanine (CAG) trinucleotide repeat in the 5'-translated region of the IT15 gene on chromosome 4, which encode the protein huntingtin . The expansions result in the formation of elongated proteins with a variety of new properties. The extent of the expansion is inversely correlated with the age of onset (AO). Nevertheless, large part of the variance in AO remains unexplained . The pathogenesis of HD has been implicated to relate to different aspects of the homocysteine metabolism: Cystathionine [beta]-synthase (CBS) appears to bind specifically to huntingtin (htt) . CBS deficiency is associated with homocystinuria, which affects various physiological systems, including the central nervous system. Homocysteine, one of the substrates of CBS accumulates in homocystinuria and is metabolized to homocysteate and homocysteine sulphinate, both components of which are amino acids with significant excitotoxic potential. In this context homocysteine was suggested to influence the pathogenesis of HD. Two common polymorphisms have been described in the MTHFR gene, both single nucleotide substitutions resulting in amino acid changes (C677T → Ala222Val and A1298C → Glu429Ala) [4, 5]. Whereas C677T unequivocally affects enzyme function and has been associated with increased plasma homocysteine concentrations and an altered balance of folate metabolites , the functional relevance in vivo of the A1298C allele is less well defined. A1298C affects enzyme function in vitro to a lesser degree, and individuals carrying the variation have frequently normal homocysteine and plasma folate concentrations [6, 7]. It is unclear whether the substitution affects folate metabolism under specific physiological conditions, e.g. under low nutrient intake. Apparently, the 677C→T and the 1298A→C polymorphisms can act synergistically, given that heterozygosity for both polymorphisms causes lower MTHFR enzymatic activity than heterozygosity alone for either of them and a trend to higher or significantly higher plasma total homocysteine levels .
Brune et al. reported recently an association between the homozygous A1298C allele and a distinctly lower AO compared to the wild type MTHFR genotypes . In the present study we re-examined the 1298A→C polymorphism as well as its potential interaction with the 677C→T polymorphism as genetic factors influencing the AO of HD. Compared to the patient cohort examined by Brune et al. (n = 171), here 27 patients have been excluded from the initial cohort due to relatedness (the first diagnosed family member remained in this study) and lacking information on the motor age at onset. In contrast to the initial cohort, exclusively the motor AO was referred to. The present cohort (n = 167) has been supplemented by 23 patients due to recruitment of new patients. The potential influence of certain genotypes on AO was calculated by linear regression, in which R2 illustrates the relative improvement of the regression model when the various genotypes are considered in addition to the HD CAG repeats.
Results and discussion
Analysis of the MTHFR 677C→T and the 1298A→C polymorphisms in 167 patients revealed allele frequencies of 0.35 for MTHFR 677T and 0.29 for MTHFR 1298C, respectively. Observed frequencies were in Hardy-Weinberg equilibrium.
Number of different genotype combinations of the MTHFR 677C→Ta and 1298 A→Cb polymorphism in 167 HD patients
n = 71
n = 75
n = 21
1298AA (n = 80)
1298AC (n = 74)
1298CC(n = 13)
Linear regression analysis concerning polymorphisms in the MTHFR gene
% additional explained variance
HD CAG + MTHFR A1298C
HD CAG + MTHFR C677T
HD CAG + compound heterozygotes
We failed to replicate the association finding between the 1298CC genotype in the MTHFR gene and earlier AO in HD. In future studies in this context, also the folate levels of individual patients should be taken into account as well as environmental factors.
One hundred sixty-seven patients clinically diagnosed as suffering from HD were ascertained for their motor AO in the Huntington Center (HZ) NRW, Bochum (Germany) . All patients gave informed consent for genotyping. The CAG repeat sizes and the MTHFR A1298C and C677T genotypes were determined as described before . The dependence of the AO on CAG repeat number was determined by linear regression. Residuals from this model were verified, and there was no evidence of departure from normality and equality of variance assumptions. The possible genotypic effects of the two polymorphisms were assessed with multiple linear regressions, while allowing for the predictive effects of the CAG repeat size. We used the AO as dependent variable and the respective genotypes as independent variables. The CAG repeat number was considered as numerical variable. All of the other putatively modifying genotypes were considered as nominal variables by assigning the value "0, 1" or "0, 1, 2" according to the subject's number of variant alleles under a model of dominance or otherwise according to a model of generalized additive allelic effect. SPSS Ver.11.0 for Windows (SPSS Inc.) was used for all statistical analyses.
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