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Investigation between the S377G3 GATA-4 polymorphism and migraine.


ABSTRACT: Migraine is a common and painful neurological disorder, with genetic and environmental components. Several conditions have been shown to be comorbid with migraine, notably a cardiac malformation affecting the interatrial septum and leading to patent foramen ovale (PFO). Mutations in the development regulatory gene GATA-4, located on human chromosome 8p23.1-p22, have been found to be responsible for some cases of congenital heart defects including PFO. To determine whether the GATA-4 gene is involved in migraine, the present study performed an association analysis of a common GATA-4 variant that results in a change of amino acid (S377G), in a large case/control population (275 unrelated Caucasian migraineurs versus 275 control individuals). The results showed that there was no significant association for this polymorphism between migraine and controls (chi(2) = 0.84, P = 0.66). Thus it appears that the GATA-4 (S377G) mutation does not play a significant role in common migraine susceptibility.

SUBMITTER: Sherin C 

PROVIDER: S-EPMC2577932 | biostudies-literature | 2008

REPOSITORIES: biostudies-literature

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Investigation between the S377G3 GATA-4 polymorphism and migraine.

Sherin Chikhani C   Francesca Fernandez F   Karl Poetter P   Brendan Toohey T   Ron Harvey H   Lyn Griffiths G  

The open neurology journal 20080725


Migraine is a common and painful neurological disorder, with genetic and environmental components. Several conditions have been shown to be comorbid with migraine, notably a cardiac malformation affecting the interatrial septum and leading to patent foramen ovale (PFO). Mutations in the development regulatory gene GATA-4, located on human chromosome 8p23.1-p22, have been found to be responsible for some cases of congenital heart defects including PFO. To determine whether the GATA-4 gene is invo  ...[more]

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