| Literature DB >> 23727859 |
David Ellinghaus1, Hansjörg Baurecht, Jorge Esparza-Gordillo, Elke Rodríguez, Anja Matanovic, Ingo Marenholz, Norbert Hübner, Heidi Schaarschmidt, Natalija Novak, Sven Michel, Laura Maintz, Thomas Werfel, Ulf Meyer-Hoffert, Melanie Hotze, Holger Prokisch, Katharina Heim, Christian Herder, Tomomitsu Hirota, Mayumi Tamari, Michiaki Kubo, Atsushi Takahashi, Yusuke Nakamura, Lam C Tsoi, Philip Stuart, James T Elder, Liangdan Sun, Xianbo Zuo, Sen Yang, Xuejun Zhang, Per Hoffmann, Markus M Nöthen, Regina Fölster-Holst, Juliane Winkelmann, Thomas Illig, Bernhard O Boehm, Richard H Duerr, Carsten Büning, Stephan Brand, Jürgen Glas, Maeve A McAleer, Caoimhe M Fahy, Michael Kabesch, Sara Brown, W H Irwin McLean, Alan D Irvine, Stefan Schreiber, Young-Ae Lee, Andre Franke, Stephan Weidinger.
Abstract
Atopic dermatitis is a common inflammatory skin disease with a strong heritable component. Pathogenetic models consider keratinocyte differentiation defects and immune alterations as scaffolds, and recent data indicate a role for autoreactivity in at least a subgroup of patients. FLG (encoding filaggrin) has been identified as a major locus causing skin barrier deficiency. To better define risk variants and identify additional susceptibility loci, we densely genotyped 2,425 German individuals with atopic dermatitis (cases) and 5,449 controls using the Immunochip array followed by replication in 7,196 cases and 15,480 controls from Germany, Ireland, Japan and China. We identified four new susceptibility loci for atopic dermatitis and replicated previous associations. This brings the number of atopic dermatitis risk loci reported in individuals of European ancestry to 11. We estimate that these susceptibility loci together account for 14.4% of the heritability for atopic dermatitis.Entities:
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Year: 2013 PMID： 23727859 PMCID： PMC3797441 DOI： 10.1038/ng.2642
Source DB: PubMed Journal: Nat Genet ISSN： 1061-4036 Impact factor: 38.330