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Freilinger, T.* ; Anttila, V.* ; de Vries, B.* ; Malik, R.* ; Kallela, M.* ; Terwindt, G.M.* ; Pozo-Rosich, P.* ; Winsvold, B.* ; Nyholt, D.R.* ; van Oosterhout, W.P.J.* ; Artto, V.* ; Todt, U.* ; Hämäläinen, E.* ; Fernandez-Morales, J.* ; Louter, M.A.* ; Kaunisto, M.A.* ; Schoenen, J.* ; Raitakari, O.* ; Lehtimäki, T.* ; Vila-Pueyo, M.* ; Göbel, H.* ; Wichmann, H.-E. ; Sintas, C.* ; Uitterlinden, A.G.* ; Hofman, A.* ; Rivadeneira, F.* ; Heinze, A.* ; Tronvik, E.* ; van Duijn, C.M.* ; Kaprio, J.* ; Cormand, B.* ; Wessman, M.* ; Frants, R.R.* ; Meitinger, T. ; Müller-Myhsok, B.* ; Zwart, J.A.* ; Färkkilä, M.* ; Macaya, A.* ; Ferrari, M.D.* ; Kubisch, C.* ; Palotie, A.* ; Dichgans, M.* ; van den Maagdenberg, A.M.J.M.*

Genome-wide association analysis identifies susceptibility loci for migraine without aura.

Nat. Genet. 44, 777-782 (2012)
DOI PMC
Open Access Green as soon as Postprint is submitted to ZB.
Migraine without aura is the most common form of migraine, characterized by recurrent disabling headache and associated autonomic symptoms. To identify common genetic variants associated with this migraine type, we analyzed genome-wide association data of 2,326 clinic-based German and Dutch individuals with migraine without aura and 4,580 population-matched controls. We selected SNPs from 12 loci with 2 or more SNPs associated with P values of <1 x 10(-5) for replication testing in 2,508 individuals with migraine without aura and 2,652 controls. SNPs at two of these loci showed convincing replication: at 1q22 (in MEF2D; replication P = 4.9 x 10(-4); combined P = 7.06 x 10(-11)) and at 3p24 (near TGFBR2; replication P = 1.0 x 10(-4); combined P = 1.17 x 10(-9)). In addition, SNPs at the PHACTR1 and ASTN2 loci showed suggestive evidence of replication (P = 0.01; combined P = 3.20 x 10(-8) and P = 0.02; combined P = 3.86 x 10(-8), respectively). We also replicated associations at two previously reported migraine loci in or near TRPM8 and LRP1. This study identifies the first susceptibility loci for migraine without aura, thereby expanding our knowledge of this debilitating neurological disorder.
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Publication type Article: Journal article
Document type Scientific Article
Keywords GENERAL-POPULATION; NEUROPATHIC PAIN; RECEPTOR; METAANALYSIS; EXPRESSION; COMMON; MEF2; HEADACHE; PROTEIN; FAMILY
ISSN (print) / ISBN 1061-4036
e-ISSN 1546-1718
Journal Nature Genetics
Quellenangaben Volume: 44, Issue: 7, Pages: 777-782 Article Number: , Supplement: ,
Publisher Nature Publishing Group
Publishing Place New York, NY
Reviewing status Peer reviewed
Institute(s) Institute of Human Genetics (IHG)
Institute of Epidemiology (EPI)