SNP variants within the vanilloid TRPV1 and TRPV3 receptor genes are associated with migraine in the Spanish population

Oriel Carreño, Roser Corominas, Jessica Fernández-Morales, Montserrat Camiña, María Jesús Sobrido, José Manuel Fernández-Fernández, Patricia Pozo-Rosich, Bru Cormand, Alfons Macaya

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    63 Citations (Scopus)


    The transient receptor potential (TRP) superfamily of non-selective cationic channels are involved in several processes plausibly relevant to migraine pathophysiology, including multimodal sensory and pain perception, central and peripheral sensitization, and regulation of calcium homeostasis. With the aim of identifying single nucleotide polymorphisms (SNPs) in TRP genes that may confer increased genetic susceptibility to migraine, we carried out a case-control genetic association study with replication, including a total of 1,040 cases and 1,037 controls. We genotyped 149 SNPs covering 14 TRP genes with known brain expression. The two-stage study comprised samples of 555 and 485 Spanish, Caucasian patients, selected according to the ICHD-II criteria for the diagnosis of migraine without aura (MO) or migraine with aura (MA). In the discovery sample, 19 SNPs in ten TRP genes showed nominal association (P<0.05) with MO, MA, or overall migraine. In the replication sample, nominal association was confirmed for TRPV3 rs7217270 in MA and TRPV1 rs222741 in the overall migraine group. Risk haplotypes were identified for seven of the genes showing nominal association in the discovery set, but none of them was replicated. The present findings suggest that members of the vanilloid TRPV subfamily of receptors contribute to the genetic susceptibility to migraine in the Spanish population. © 2011 Wiley Periodicals, Inc.
    Original languageEnglish
    Pages (from-to)94-103
    JournalAmerican Journal of Medical Genetics, Part B: Neuropsychiatric Genetics
    Volume159 B
    Issue number1
    Publication statusPublished - 1 Jan 2012


    • Association study
    • Migraine
    • TRP
    • Vanilloid


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