Frequency of the C677T variant of the methylenetetrahydrofolate reductase (MTHFR) gene in patients with migraine with or without aura – a preliminary report

Neurologia i Neurochirurgia Polska - Tập 46 - Trang 443-449 - 2012
Dorota Szczygioł1, Ewa Motta1, Anna Gołba1, Arkadiusz Stęposz1, Joanna Witecka2, Marek Dębski1, Daria Błaszkiewicz1, Aleksander Sieroń2
1Oddział Neurologii SPSK nr 7, Śląski Uniwersytet Medyczny w Katowicach
2Katedra i Zakład Biologii Ogólnej, Molekularnej i Genetyki, Śląski Uniwersytet Medyczny w Katowicach

Tài liệu tham khảo

Nowakowski, 2007, Migrena – implikacje patofizjologiczno-terapeutyczne, Pol Przegl Med Lotn, 1, 85 Lea, 2004, The methylenotetrahydrofolate reductase gene variant C677T influences susceptibility to migraine with aura, BMC Medicine, 2, 3, 10.1186/1741-7015-2-3 Oterino, 2004, MTHFR T677 homozygosis influences the presence of aura in migreneurs, Cephalgia, 24, 491, 10.1111/j.1468-2982.2004.00692.x Schürks, 2010, MTHFR 677C>T and ACE D/I polymorphisms in migraine: a systematic review and meta-analysis, Headache, 50, 588, 10.1111/j.1526-4610.2009.01570.x Wichlińska-Lipka, 2008, Rola homocysteiny w patogenezie chorób układu nerwowego, Forum Med Rodz, 2, 223 Piechowski-Jóźwiak, 2005, Rola drożnego otworu owalnego w patogenezie udaru niedokrwiennego, Kardiologia po Dyplomie, 3, 26 Headache Classification Committee of the International Headache Society, 2004, Classification and diagnostic criteria for headache disorders, cranial neuralgias, and facial pain, 2nd edition, Cephalalgia, 24, 1 Kowa, 2000, The homozygous C677T mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for migraine, Am J Med Genet, 96, 762, 10.1002/1096-8628(20001204)96:6<762::AID-AJMG12>3.0.CO;2-X Marcus, 1992, Estimation of cerebrovascular reactivity using transcranial doppler, including the use of breathholding as the vasodilatory stimulus, Stroke, 23, 669 Jauss, 2000, Detection of right-to-left shunt with ultrasound contrast agent and transcranial Doppler sonography, Cerebrovasc Dis, 10, 490, 10.1159/000016119 Kozera, 2004, Próba TCD na PFO – znaczenie kliniczne i ograniczenia, Pol Przegl Neurol, 4, 58 Domitrz, 2004, Występowanie drożnego otworu owalnego u pacjentów z migreną, Neurol Neurochir Pol, 38, 89 Tietjen, 2007, Migraine and ischaemic heart disease and stroke: potential mechanisms and treatment implications, Cephalgia, 27, 981, 10.1111/j.1468-2982.2007.01407.x de Tommaso, 2007, Influence of MTHFR genotype on contingent negative variation and MRI abnormalities in migraine, Headache, 47, 253, 10.1111/j.1526-4610.2006.00690.x Pezzini, 2007, Migraine mediates the influence of C667T MTHFR genotypes on ischemic stroke risk with a stroke-subtype effect, Stroke, 38, 3145, 10.1161/STROKEAHA.107.491506 Schürks, 2008, Interrelationships among the MTHFR 677C>T polymorphism, migraine, and cardiovascular disease, Neurology, 71, 505, 10.1212/01.wnl.0000316198.34558.e5 Ferro, 2008, The C677T polymorphism in MTHFR is not associated with migraine in Portugal, Dis Markers, 25, 107, 10.1155/2008/178679 Bottini, 2006, Metabolic and genetic risk factors for migraine in children, Cephalgia, 26, 731, 10.1111/j.1468-2982.2006.01107.x Kara, 2003, Association of the C677T and A1298C polymorphisms in the 5,10 methylenetetrahydrofolate reductase gene in patients with migraine risk, Brain Res Mol Brain Res, 111, 84, 10.1016/S0169-328X(02)00672-1 Kaunisto, 2006, Testing of variants of the MTHFR and ESR1 genes in 1798 Finnish individuals fails to confirm the association with migraine with aura, Cephalalgia, 26, 1462, 10.1111/j.1468-2982.2006.01228.x Oterino, 2005, Thymidylate synthase promoter tandem repeat and MTHFD1 R 653Q polymorphisms modulate the risk for migraine conferred by the MTHFR T677 allele, Brain Res Mol Brain Res, 139, 163, 10.1016/j.molbrainres.2005.05.015 Scher, 2006, Me and MTHFR C677T genotype in population-based sample, Ann Neurol, 59, 372, 10.1002/ana.20755 Todt, 2006, MTHFR C677T polymorphism and migraine with aura, Ann Neurol, 60, 621, 10.1002/ana.20911 Liu, 2010, Analysis of the MTHFR C677T variant with migraine phenotypes, BMC Res Notes, 28, 213, 10.1186/1756-0500-3-213 Schürks, 2010, MTHFR 677C>T and ACE D/I polymorphisms in migraine. A systematic review and meta-analysis, Headache, 50, 588, 10.1111/j.1526-4610.2009.01570.x Lea, 2009, The effects of vitamin supplementation and MTHFR(C677T) genotype on homocysteine-lowering and migraine disability, Pharmacogenet Genomics, 19, 422, 10.1097/FPC.0b013e32832af5a3 Hering Hanit, 2001, Is blood homocysteine elevated in migraine?, Headache, 41, 779, 10.1046/j.1526-4610.2001.01143.x Oterino, 2010, The relationship between homocysteine and genes of folate-related enzymes in migraine patients, Headache, 50, 99, 10.1111/j.1526-4610.2009.01484.x Rigatelli, 2008, Migraine and patent foramen ovale: connecting flight or one way ticket?, Expert Rev Neurother, 8, 1331, 10.1586/14737175.8.9.1331 Del Sette, 2008, White matter lesions in migraine and right-to-left shunt: a conventional and diffusion MRI study, Cephalalgia, 28, 376, 10.1111/j.1468-2982.2008.01544.x Bosca, 2008, Estudio de la relacion entre lesiones de sustancia blanca en la resonancia magnetica y foramen oval permeable en pacientes con migrana, Neurologia, 23, 499