Single-nucleotide polymorphism alleles in the insulin receptor gene are associated with typical migraine

Genomics. 2001 Dec;78(3):135-49. doi: 10.1006/geno.2001.6647.

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.

MeSH terms

  • Alleles*
  • 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
  • Migraine Disorders / genetics*
  • Polymorphism, Single Nucleotide*
  • Protein Binding
  • Receptor, Insulin / genetics*
  • Receptor, Insulin / metabolism
  • Reproducibility of Results
  • White People / genetics

Substances

  • DNA Primers
  • Receptor, Insulin