MTHFR T677 homozygosis influences the presence of aura in migraineurs

Authors


Dr. Agustín Oterino, Service of Neurology, University Hospital Marqués de Valdecilla, 39008  Santander, Spain. Tel. +349 4220 2655, fax  +349 4220 2507,  e-mail: oterinoa@unican.es

Abstract

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It has been suggested that folate metabolism could be involved in migraine pathogenesis. We analysed the 5′,10′-methylenetetrahydrofolate reductase (MTHFR) genotypic distribution in a large migraine sample. We genotyped 230 migraine patients (152 migraine without aura (MO) and 78 migraine with aura (MA)) and 204 nonheadache controls. The incidence of TT homozygosis for migraine in general (12%), MO (9%) and MA (18%) did not significantly differ from that found in healthy controls (13%). Differences were significant when the frequency of TT homozygosis between MA and MO (P = 0.03, OR = 2.34, 95% CI = 1.04–5.26) was compared. There was a tendency for a higher frequency of the MTHFR T allele in the MA group (42%) as compared to MO (29%) and controls (36%). These differences were significant only in the case of MA vs. MO (P = 0.006, OR = 1.75, 95% CI = 1.15–2.65). These results could indicate that the MTHFR C677T polymorphism, causing mild hyperhomocystinaemia, might be a genetic risk factor for experiencing aura among migraineurs. Overall, however, there was no association between  migraine  and the C677T  MTHFR  polymorphism. 

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