Migraine with aura susceptibility locus on chromosome 19p13 is distinct from the familial hemiplegic migraine locus.

Published

Journal Article

Migraine is a common neurological disease with a major genetic component. Recently, it has been proposed that a single locus on chromosome 19p13 contributes to the genetic susceptibility of both rare familial hemiplegic migraine (FHM) and more common types of migraine, migraine with aura and migraine without aura. We analyzed 16 families for co-segregation of migraine with aura and chromosome 19p13 markers. Using multipoint model-free linkage analysis, we obtained a lod score of 4.28 near D19S592. Using an affecteds-only model of linkage, we observed a lod score of 4.79 near D19S592. We were able to provide statistical evidence that this locus on chromosome 19p13 is most likely not the gene CACNA1A, mutations in which cause FHM. These data indicate that chromosome 19p13 contains a locus which contributes to the genetic susceptibility of migraine with aura that is distinct from the FHM locus.

Full Text

Duke Authors

Cited Authors

  • Jones, KW; Ehm, MG; Pericak-Vance, MA; Haines, JL; Boyd, PR; Peroutka, SJ

Published Date

  • December 2001

Published In

Volume / Issue

  • 78 / 3

Start / End Page

  • 150 - 154

PubMed ID

  • 11735221

Pubmed Central ID

  • 11735221

International Standard Serial Number (ISSN)

  • 0888-7543

Digital Object Identifier (DOI)

  • 10.1006/geno.2001.6665

Language

  • eng

Conference Location

  • United States