| Literature DB >> 17116097 |
M A Kaunisto1, M Kallela, E Hämäläinen, R Kilpikari, H Havanka, H Harno, M Nissilä, E Säkö, M Ilmavirta, J Liukkonen, H Teirmaa, O Törnwall, M Jussila, J Terwilliger, M Färkkilä, J Kaprio, A Palotie, M Wessman.
Abstract
Among the few independently replicated genetic associations in migraine are polymorphisms in the methylenetetrahydrofolate reductase (MTHFR) and oestrogen receptor (ESR1) genes. We studied the contribution of these genes to migraine susceptibility by genotyping six MTHFR and 26 ESR1 polymorphisms in 898 unrelated migraine with aura (MA) patients and in 900 unrelated healthy controls. There were no differences in the genotype distributions of the previously migraine-associated SNPs C677T (MTHFR) and G2014A (ESR1) between cases and controls (P-values 0.83 and 0.55, respectively). Thus, we were not able to replicate the previous findings, although our study had considerable power. However, five of the ESR1 SNPs (rs6557170, rs2347867, rs6557171, rs4870062 and rs1801132) that were in strong linkage disequilibrium were nominally associated with MA (uncorrected P-values 0.007-0.034). These results did not, however, remain significant after taking multiple testing into account. Thus it seems unlikely that the studied genes are involved in migraine susceptibility, at least in this sample.Entities:
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Year: 2006 PMID： 17116097 DOI： 10.1111/j.1468-2982.2006.01228.x
Source DB: PubMed Journal: Cephalalgia ISSN： 0333-1024 Impact factor: 6.292