The methylenetetrahydrofolate reductase gene variant C677T influences susceptibility to migraine with aura

<p>Abstract</p> <p>Background</p> <p>The C677T variant in the methylenetetrahydrofolate reductase (MTHFR) gene is associated with increased levels of circulating homocysteine and is a mild risk factor for vascular disease. Migraine, with and without aura (MA and MO), is...

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Main Authors: Sundholm James, Ovcaric Micky, Lea Rod A, MacMillan John, Griffiths Lyn R
Format: Article
Language:English
Published: BMC 2004-02-01
Series:BMC Medicine
Subjects:
Online Access:http://www.biomedcentral.com/1741-7015/2/3
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spelling doaj-0564a80f97df4eea8ba0b6a2138093b32020-11-25T00:33:28ZengBMCBMC Medicine1741-70152004-02-0121310.1186/1741-7015-2-3The methylenetetrahydrofolate reductase gene variant C677T influences susceptibility to migraine with auraSundholm JamesOvcaric MickyLea Rod AMacMillan JohnGriffiths Lyn R<p>Abstract</p> <p>Background</p> <p>The C677T variant in the methylenetetrahydrofolate reductase (MTHFR) gene is associated with increased levels of circulating homocysteine and is a mild risk factor for vascular disease. Migraine, with and without aura (MA and MO), is a prevalent and complex neurovascular disorder that may also be affected by genetically influenced hyperhomocysteinaemia. To determine whether the C677T variant in the MTHFR gene is associated with migraine susceptibility we utilised unrelated and family-based case-control study designs.</p> <p>Methods</p> <p>A total of 652 Caucasian migraine cases were investigated in this study. The MTHFR C677T variant was genotyped in 270 unrelated migraine cases and 270 controls as well as 382 affected subjects from 92 multiplex pedigrees.</p> <p>Results</p> <p>In the unrelated case-control sample we observed an over-representation of the 677T allele in migraine patients compared to controls, specifically for the MA subtype (40% vs. 33%) (χ<sup>2 </sup>= 5.70, <it>P </it>= 0.017). The Armitage test for trend indicated a significant dosage effect of the risk allele (T) for MA (χ<sup>2 </sup>= 5.72, <it>P </it>= 0.017). This linear trend was also present in the independent family-based sample (χ<sup>2 </sup>= 4.25, <it>P</it><sub><it>adjusted </it></sub>= 0.039). Overall, our results indicate that the T/T genotype confers a modest, yet significant, increase in risk for the MA subtype (odds ratio: 2.0 – 2.5). No increased risk for the MO subtype was observed (<it>P </it>> 0.05).</p> <p>Conclusions</p> <p>In Caucasians, the C677T variant in the MTHFR gene influences susceptibility to MA, but not MO. Investigation into the enzyme activity of MTHFR and the role of homocysteine in the pathophysiology of migraine is warranted.</p> http://www.biomedcentral.com/1741-7015/2/3migraineassociationMTHFRgenevariant
collection DOAJ
language English
format Article
sources DOAJ
author Sundholm James
Ovcaric Micky
Lea Rod A
MacMillan John
Griffiths Lyn R
spellingShingle Sundholm James
Ovcaric Micky
Lea Rod A
MacMillan John
Griffiths Lyn R
The methylenetetrahydrofolate reductase gene variant C677T influences susceptibility to migraine with aura
BMC Medicine
migraine
association
MTHFR
gene
variant
author_facet Sundholm James
Ovcaric Micky
Lea Rod A
MacMillan John
Griffiths Lyn R
author_sort Sundholm James
title The methylenetetrahydrofolate reductase gene variant C677T influences susceptibility to migraine with aura
title_short The methylenetetrahydrofolate reductase gene variant C677T influences susceptibility to migraine with aura
title_full The methylenetetrahydrofolate reductase gene variant C677T influences susceptibility to migraine with aura
title_fullStr The methylenetetrahydrofolate reductase gene variant C677T influences susceptibility to migraine with aura
title_full_unstemmed The methylenetetrahydrofolate reductase gene variant C677T influences susceptibility to migraine with aura
title_sort methylenetetrahydrofolate reductase gene variant c677t influences susceptibility to migraine with aura
publisher BMC
series BMC Medicine
issn 1741-7015
publishDate 2004-02-01
description <p>Abstract</p> <p>Background</p> <p>The C677T variant in the methylenetetrahydrofolate reductase (MTHFR) gene is associated with increased levels of circulating homocysteine and is a mild risk factor for vascular disease. Migraine, with and without aura (MA and MO), is a prevalent and complex neurovascular disorder that may also be affected by genetically influenced hyperhomocysteinaemia. To determine whether the C677T variant in the MTHFR gene is associated with migraine susceptibility we utilised unrelated and family-based case-control study designs.</p> <p>Methods</p> <p>A total of 652 Caucasian migraine cases were investigated in this study. The MTHFR C677T variant was genotyped in 270 unrelated migraine cases and 270 controls as well as 382 affected subjects from 92 multiplex pedigrees.</p> <p>Results</p> <p>In the unrelated case-control sample we observed an over-representation of the 677T allele in migraine patients compared to controls, specifically for the MA subtype (40% vs. 33%) (χ<sup>2 </sup>= 5.70, <it>P </it>= 0.017). The Armitage test for trend indicated a significant dosage effect of the risk allele (T) for MA (χ<sup>2 </sup>= 5.72, <it>P </it>= 0.017). This linear trend was also present in the independent family-based sample (χ<sup>2 </sup>= 4.25, <it>P</it><sub><it>adjusted </it></sub>= 0.039). Overall, our results indicate that the T/T genotype confers a modest, yet significant, increase in risk for the MA subtype (odds ratio: 2.0 – 2.5). No increased risk for the MO subtype was observed (<it>P </it>> 0.05).</p> <p>Conclusions</p> <p>In Caucasians, the C677T variant in the MTHFR gene influences susceptibility to MA, but not MO. Investigation into the enzyme activity of MTHFR and the role of homocysteine in the pathophysiology of migraine is warranted.</p>
topic migraine
association
MTHFR
gene
variant
url http://www.biomedcentral.com/1741-7015/2/3
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