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Genomics ; 78(3): 135-49, 2001 Dec.
Article in English | MEDLINE | ID: mdl-11735220

ABSTRACT

We have identified a migraine locus on chromosome 19p13.3/2 using linkage and association analysis. We isolated 48 single-nucleotide polymorphisms within the locus, of which we genotyped 24 in a Caucasian population comprising 827 unrelated cases and 765 controls. Five single-nucleotide polymorphisms within the insulin receptor gene showed significant association with migraine. This association was independently replicated in a case-control population collected separately. We used experiments with insulin receptor RNA and protein to investigate functionality for the migraine-associated single-nucleotide polymorphisms. We suggest possible functions for the insulin receptor in migraine pathogenesis.


Subject(s)
Alleles , Migraine Disorders/genetics , Polymorphism, Single Nucleotide , Receptor, Insulin/genetics , Base Sequence , Case-Control Studies , Chromosome Mapping , Chromosomes, Artificial, Bacterial , Chromosomes, Human, Pair 19 , DNA Primers , Female , Genetic Predisposition to Disease , Genotype , Humans , Linkage Disequilibrium , Male , Protein Binding , Receptor, Insulin/metabolism , Reproducibility of Results , White People/genetics
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