• van den MaagdenbergArn M J MAMJM0000-0002-9310-5535Department of Human Genetics, Leiden University Medical Centre, Leiden, The Netherlands. a.m.j.m.van_den_Maagdenberg@lumc.nl.Department of Neurology, Leiden University Medical Centre, 9600, 2300 RC, Leide, Dale R Nyholt, and Verneri Anttila.
• Department of Human Genetics, Leiden University Medical Centre, Leiden, The Netherlands. a.m.j.m.van_den_Maagdenberg@lumc.nl.
• J Headache Pain. 2019 Jan 11; 20 (1): 55.

AbstractRecent technical advances in genetics made large-scale genome-wide association studies (GWAS) in migraine feasible and have identified over 40 common DNA sequence variants that affect risk for migraine types. Most of the variants, which are all single nucleotide polymorphisms (SNPs), show robust association with migraine as evidenced by the fact that the vast majority replicate in subsequent independent studies. However, despite thorough bioinformatic efforts aimed at linking the migraine risk SNPs with genes and their molecular pathways, there remains quite some discussion as to how successful this endeavour has been, and their current practical use for the diagnosis and treatment of migraine patients. Although existing genetic information seems to favour involvement of vascular mechanisms, but also neuronal and other mechanisms such as metal ion homeostasis and neuronal migration, the complexity of the underlying genetic pathophysiology presents challenges to advancing genetic knowledge to clinical use. A major issue is to what extent one can rely on bioinformatics to pinpoint the actual disease genes, and from this the linked pathways. In this Commentary, we will provide an overview of findings from GWAS in migraine, current hypotheses of the disease pathways that emerged from these findings, and some of the major drawbacks of the approaches used to identify the genes and pathways. We argue that more functional research is urgently needed to turn the hypotheses that emerge from GWAS in migraine to clinically useful information.

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