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Dieudé, P.* ; Bouaziz, M.* ; Guedj, M.* ; Riemekasten, G.* ; Airo, P.* ; Müller, M. ; Cusi, D.* ; Matucci-Cerinic, M.* ; Melchers, I.* ; Koenig, W.* ; Salvi, E.* ; Wichmann, H.-E. ; Cuomo, G.* ; Hachulla, E.* ; Diot, E.* ; Hunzelmann, N.* ; Caramaschi, P.* ; Mouthon, L.* ; Riccieri, V.* ; Distler, J.* ; Tarner, I.* ; Avouac, J.* ; Meyer, O.* ; Kahan, A.* ; Chiocchia, G.* ; Boileau, C.* ; Allanore, Y.*

Evidence of the contribution of the X chromosome to systemic sclerosis susceptibility: Association with the functional IRAK1 196Phe/532Ser haplotype.

Arthritis Rheum. 63, 3979-3987 (2011)
Verlagsversion DOI PMC
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Open Access Green möglich sobald Postprint bei der ZB eingereicht worden ist.
Several autoimmune disorders, including systemic sclerosis (SSc), are characterized by a strong sex bias. To date, it is not known whether genes on the sex chromosomes influence SSc susceptibility. Recently, an IRAK1 haplotype that contains the 196Phe functional variant (rs1059702), located on Xq28, was found to confer susceptibility to systemic lupus erythematosus (SLE). This study was undertaken to test for an association between SSc and the IRAK1 SLE risk haplotype. We tested for an association with the IRAK1 SLE risk haplotype in a discovery set of 849 SSc patients and 625 controls. IRAK1 rs1059702 was further genotyped in a replication set, which included Caucasian women from Italy (493 SSc patients and 509 controls) and Germany (466 SSc patients and 1,083 controls. An association between the IRAK1 haplotype and SSc was detected in the discovery set. In both the discovery and replication sets, the rs1059702 TT genotype was found to be associated with specific SSc subsets, highlighting a potential contribution to disease severity. A meta-analysis provided evidence of an association of both the T allele and TT genotype with the overall disease, with an odds ratio (OR) of 1.20 and 95% confidence interval (95% CI) of 1.06-1.35 for the T allele (P = 0.003) and an OR of 1.49 and 95% CI of 1.06-2.10 for the TT genotype (P = 0.023). However, the most notable associations were observed with the diffuse cutaneous, anti-topoisomerase I antibody positive, and SSc-related fibrosing alveolitis subsets (OR 2.35 [95% CI 1.51-3.66], P = 1.56 × 10(-4), OR 2.84 [95% CI 1.87-4.32], P = 1.07 × 10(-6), and OR 2.09 [95% CI 1.35-3.24], P = 9.05 × 10(-4), respectively). Our study provides the first evidence of an association between IRAK1 and SSc, demonstrating that a sex chromosome gene directly influences SSc susceptibility and its phenotypic heterogeneity.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter genetic risk-factor; nf-kappa-b; lupus-erythematosus; innate-immunity; disease; scleroderma; activation; variant; irf5; pathogenesis
Sprache englisch
Veröffentlichungsjahr 2011
HGF-Berichtsjahr 2011
ISSN (print) / ISBN 0004-3591
e-ISSN 1529-0131
Zeitschrift Arthritis & Rheumatology
Quellenangaben Band: 63, Heft: 12, Seiten: 3979-3987 Artikelnummer: , Supplement: ,
Verlag Wiley
Verlagsort Atlanta, USA
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Genetic Epidemiology (IGE)
Institute of Epidemiology (EPI)
POF Topic(s) 30501 - Systemic Analysis of Genetic and Environmental Factors that Impact Health
30503 - Chronic Diseases of the Lung and Allergies
Forschungsfeld(er) Genetics and Epidemiology
PSP-Element(e) G-504100-001
G-503900-001
PubMed ID 21898345
DOI 10.1002/art.30640
Scopus ID 82455198713
Erfassungsdatum 2011-12-31
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