The association between candidate migraine susceptibility loci and severe migraine phenotype in a clinical sample. (June 2016)

• Record Type: Journal Article
• Authors: Esserlind, Ann-Louise; Christensen, Anne Francke; Steinberg, Stacy; Grarup, Niels; Pedersen, Oluf; Hansen, Torben; Werge, Thomas; Hansen, Thomas Folkmann; Husemoen, Lise Lotte N; Linneberg, Allan; Budtz-Jorgensen, Esben; Westergaard, Maria Lurenda; Stefansson, Hreinn; Olesen, Jes
• Is Part Of: Cephalalgia. Volume 36:Number 7(2016)
• Page Start: 615
• Page End: 623
• Publication Date: 2016-06
• Subjects: Migraine -- clinic-based sample -- replication -- genetics -- susceptibility loci -- genome-wide association studies; Headache -- Periodicals; 616.8491
• DOI: 10.1177/0333102415570492
• Languages: English
• ISSNs: 0333-1024

Abstract

Introduction: The objective of the study was to follow up and to test whether 12 previously identified migraine-associated single nucleotide polymorphisms were associated as risk factors and/or modifying factors for severe migraine traits in a Danish clinic-based population. Methods: Semi-structured migraine interviews, blood sampling and genotyping were performed on 1806 unrelated migraineurs recruited from the Danish Headache Center. Genotyping was also performed on a control group of 6415 people with no history of migraine. Association analyses were carried out using logistic regression and odds ratios were calculated assuming an additive model for risk. The proxies for severe migraine traits (early onset of migraine; many lifetime attacks, prolonged migraine and tendency to chronification of migraine) were tested against the 12 single nucleotide polymorphisms and a combined genetic score in both a case-control and case-only logistic regression model. Results: We successfully replicated five out of the 12 previously reported loci and confirmed the same direction of effects for all the 12 single nucleotide polymorphisms. In line with the recently published genome-wide association meta-analysis, the associations were significant for all migraine and migraine without aura but not for migraine with typical aura. Two single nucleotide polymorphisms (rs2274316 and rs11172113) conferred risk of many lifetime attacks inthe case-control analysis. In the case-only analysis, only three single nucleotide polymorphisms showed nominal association with many lifetime attacks and prolonged migraine attacks. Conclusion: Our study supports previously reported findings on the association of several single nucleotide polymorphisms with migraine. It also suggests that the migraine susceptibility loci may be risk factors for severe migraine traits.