|
Migraine Disorders
|
|
0.100 |
GeneticVariation
|
BEFREE |
Expert opinion: Determination of MTHFR C677T polymorphisms as well as measurement of homocysteine concentrations may be useful to migraine patients, particularly those suffering from migraine with aura.
|
30451038 |
2019 |
|
Migraine Disorders
|
|
0.100 |
GeneticVariation
|
BEFREE |
In adult studies the MTHFR C677T polymorphism has been associated with an increased risk of migraine, but little research has been done in this area in children.
|
30170616 |
2018 |
|
Migraine Disorders
|
|
0.100 |
GeneticVariation
|
BEFREE |
Present data provide evidence for the association of rs4846049 and C677T polymorphisms in the MTHFR gene and migraine.
|
29379315 |
2018 |
|
Migraine Disorders
|
|
0.100 |
GeneticVariation
|
BEFREE |
In this genetic association study, the prevalence of the functionally relevant polymorphisms C677T in the MTHFR gene and I/D polymorphism in the ACE gene was compared in 420 patients with migraine vs 258 migraine-free controls using a chi-square statistic and binary logistic regression.
|
27483173 |
2016 |
|
Migraine Disorders
|
|
0.100 |
GeneticVariation
|
BEFREE |
We conclude that the C677T MTHFR polymorphism, responsible for a reduction of the MTHFR activity in folate metabolism, may act as a genetic susceptibility factor for migraine, MA in particular among the subjects of Asian descent.
|
24183284 |
2014 |
|
Migraine Disorders
|
|
0.100 |
GeneticVariation
|
BEFREE |
We have analyzed clinical and electrophysiological characteristics of 83 patients with migraine (migraine with aura (MA), 19 patients, and migraine without aura (MO), 64 patients, according to the ICHD-II (2003)) taking into account their genotypes of C677T variant of MTHFR.
|
23915182 |
2013 |
|
Migraine Disorders
|
|
0.100 |
GeneticVariation
|
BEFREE |
Our data suggested that MTHFR C677T polymorphism plays a role in Chinese migraine susceptibility, especially in MO.
|
23811028 |
2013 |
|
Migraine Disorders
|
|
0.100 |
GeneticVariation
|
BEFREE |
Frequency of the C677T variant of the methylenetetrahydrofolate reductase (MTHFR) gene in patients with migraine with or without aura - a preliminary report.
|
23161188 |
2013 |
|
Migraine Disorders
|
|
0.100 |
GeneticVariation
|
BEFREE |
BMIs were significantly lower in the control than the migraine group (p = 0.021); however, an association between the C677T variant and BMI was not found (p = 0.787) in the migraine group.
|
23975093 |
2013 |
|
Migraine Disorders
|
|
0.100 |
GeneticVariation
|
BEFREE |
By multivariate logistic stepwise regression analysis, type of migraine, regular and sufficient dietary intake, and methylenetetrahydrofolate reductase (MTHFR) C677T (rs1801133) and dopamine D2 receptor (DRD2) C939T (rs6275) polymorphisms were selected as significant factors that contribute independently to the development from migraine to MOH (P < 0.05).
|
22290307 |
2013 |
|
Migraine Disorders
|
|
0.100 |
GeneticVariation
|
BEFREE |
Using the multivariate analysis, three gene polymorphisms including monoamine oxidase A (MAOA) T941G, methylenetetrahydrofolate reductase (MTHFR) C677T, and tumor necrosis factor beta (TNF-β) G252Α, and the neuroticism and conscientiousness scores in NEO-FFI were selected as significant factors that independently contributed to the pathogenesis of migraine.
|
22193458 |
2012 |
|
Migraine Disorders
|
|
0.100 |
GeneticVariation
|
BEFREE |
When the vitamin-treated group was stratified by genotype, the C allele carriers of the MTHFR C677T variant showed a higher reduction in homocysteine levels (P<0.001), severity of pain in migraine (P=0.01) and percentage of high migraine disability (P=0.009) compared with those with the TT genotypes.
|
22926161 |
2012 |
|
Migraine Disorders
|
|
0.100 |
GeneticVariation
|
BEFREE |
Individuals with migraine (n = 447) were selected from the Depression Case Control (DeCC) study to investigate the association between migraine and MTHFR C677T single nucleotide polymorphism (SNP) rs1801133 using an additive model compared to non-migraineurs adjusting for depression status.
|
21635773 |
2011 |
|
Migraine Disorders
|
|
0.100 |
GeneticVariation
|
BEFREE |
Homozygosity for the methylenetetrahydrofolate reductase (MTHFR) 677C>T mutation (MTHFR TT) has been linked to an increased risk for stroke, coronary artery disease, and migraine headaches.
|
21270470 |
2011 |
|
Migraine Disorders
|
|
0.100 |
GeneticVariation
|
BEFREE |
Thirteen studies investigated the association between the MTHFR 677C>T polymorphism and migraine.
|
19925624 |
2010 |
|
Migraine Disorders
|
|
0.100 |
GeneticVariation
|
BEFREE |
MTHFR 677C->T and ACE D/I polymorphisms and migraine attack frequency in women.
|
19673907 |
2010 |
|
Migraine Disorders
|
|
0.100 |
GeneticVariation
|
BEFREE |
Association of von Willebrand factor activity with ACE I/D and MTHFR C677T polymorphisms in migraine.
|
19298544 |
2009 |
|
Migraine Disorders
|
|
0.100 |
GeneticVariation
|
BEFREE |
No significant differences in genotype and allelic frequencies of MTHFR C677T polymorphism were found on comparing migraine patients with either disease controls or healthy controls.
|
19081115 |
2009 |
|
Migraine Disorders
|
|
0.100 |
GeneticVariation
|
BEFREE |
Association of the C677T polymorphism in the MTHFR gene with migraine: a meta-analysis.
|
17714520 |
2009 |
|
Migraine Disorders
|
|
0.100 |
GeneticVariation
|
BEFREE |
Thus, we conclude that the C677T MTHFR polymorphism, responsible for a reduction of the MTHFR activity in folate metabolism, is not a major genetic susceptibility factor for migraine in the Portuguese population.
|
18957721 |
2008 |
|
Migraine Disorders
|
|
0.100 |
GeneticVariation
|
BEFREE |
Migraine mediates the influence of C677T MTHFR genotypes on ischemic stroke risk with a stroke-subtype effect.
|
17962595 |
2007 |
|
Migraine Disorders
|
|
0.100 |
GeneticVariation
|
BEFREE |
MTHFR gene variants C677T and A1298C seem to be related to an increased risk of migraine.
|
17927652 |
2007 |
|
Migraine Disorders
|
|
0.100 |
GeneticVariation
|
BEFREE |
The MTHFR C677T genotype has been associated with increased risk of migraine, particularly of migraine with aura (MA) in selected clinical samples and with elevated homocysteine.
|
17300365 |
2007 |
|
Migraine Disorders
|
|
0.100 |
GeneticVariation
|
BEFREE |
Mutations in 3 different genes responsible for familial hemiplegic migraine, a monogenetic subtype of migraine with aura, and the MTHFR C677T polymorphism in common forms of migraine are clear examples.
|
16866710 |
2006 |
|
Migraine Disorders
|
|
0.100 |
GeneticVariation
|
BEFREE |
Migraine and MTHFR C677T genotype in a population-based sample.
|
16365871 |
2006 |