Publication: Brief Report: IRF4 Newly Identified as a Common Susceptibility Locus for Systemic Sclerosis and Rheumatoid Arthritis in a Cross-Disease Meta-Analysis of Genome-Wide Association Studies.
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Date
2016
Authors
López-Isac, Elena
Martín, Jose-Ezequiel
Assassi, Shervin
Simeón, Carmen P
Carreira, Patricia
Ortego-Centeno, Norberto
Freire, Mayka
Beltrán, Emma
Narváez, Javier
Alegre-Sancho, Juan J
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Abstract
Systemic sclerosis (SSc) and rheumatoid arthritis (RA) are autoimmune diseases that have similar clinical and immunologic characteristics. To date, several shared SSc-RA genetic loci have been identified independently. The aim of the current study was to systematically search for new common SSc-RA loci through an interdisease meta-genome-wide association (meta-GWAS) strategy. The study was designed as a meta-analysis combining GWAS data sets of patients with SSc and patients with RA, using a strategy that allowed identification of loci with both same-direction and opposite-direction allelic effects. The top single-nucleotide polymorphisms were followed up in independent SSc and RA case-control cohorts. This allowed an increase in the sample size to a total of 8,830 patients with SSc, 16,870 patients with RA, and 43,393 healthy controls. This cross-disease meta-analysis of the GWAS data sets identified several loci with nominal association signals (P This study identified a novel shared locus, IRF4, for the risk of SSc and RA, and highlighted the usefulness of a cross-disease GWAS meta-analysis strategy in the identification of common risk loci.
Description
MeSH Terms
Arthritis, Rheumatoid
Genetic Loci
Genetic Predisposition to Disease
Genome-Wide Association Study
Humans
Interferon Regulatory Factors
Risk Factors
Scleroderma, Systemic
Genetic Loci
Genetic Predisposition to Disease
Genome-Wide Association Study
Humans
Interferon Regulatory Factors
Risk Factors
Scleroderma, Systemic