Investigation of the IL23R gene in a Spanish rheumatoid arthritis cohort

被引:48
作者
Orozco, Gisela
Rueda, Blanca
Robledo, Gema
Garcia, Antonio
Martin, Javier [1 ]
机构
[1] CSIC, Granada, Spain
[2] Hosp Virgen Las Nieves, Serv Reumatol, Granada, Spain
关键词
rheumatoid arthritis; genetics; polymorphism; susceptibility; IL23R gene;
D O I
10.1016/j.humimm.2007.05.008
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Recently, a genome-wide association study identified the interleukin-23 receptor gene (IL23R) as an inflammatory bowel disease (IBD) associated gene. Given the involvement of IL23R in T-cell regulation, we decided to test whether this gene is associated with rheumatoid arthritis (RA). Eight IL23R gene polymorphisms (rs1004819, rs7517847, rs10489629, rs11209026, rs1343151, rs10889677, rs11209032, and rs1495965) were selected among the 10 most associated SNPs from the IBD study. A total of 322 RA patients and 342 healthy controls were genotyped for the selected SNPs using a Taqman 5' allelic discrimination assay. We did not find statistically significant differences when we compared allele and genotype frequencies between RA patients and controls for none of the IL23R gene polymorphisms under study. We did not observe significant differences when RA patients were stratified according to their clinical and demographic features. We conclude that the IL23R gene does not seem to be associated with RA predisposition in a Spanish population. (c) 2007 American Society for Histocompatibilty and Immunogenetics. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:681 / 684
页数:4
相关论文
共 32 条
[1]   Interleukin-23 promotes a distinct CD4 T cell activation state characterized by the production of interleukin-17 [J].
Aggarwal, S ;
Ghilardi, N ;
Xie, MH ;
de Sauvage, FJ ;
Gurney, AL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (03) :1910-1914
[2]   THE AMERICAN-RHEUMATISM-ASSOCIATION 1987 REVISED CRITERIA FOR THE CLASSIFICATION OF RHEUMATOID-ARTHRITIS [J].
ARNETT, FC ;
EDWORTHY, SM ;
BLOCH, DA ;
MCSHANE, DJ ;
FRIES, JF ;
COOPER, NS ;
HEALEY, LA ;
KAPLAN, SR ;
LIANG, MH ;
LUTHRA, HS ;
MEDSGER, TA ;
MITCHELL, DM ;
NEUSTADT, DH ;
PINALS, RS ;
SCHALLER, JG ;
SHARP, JT ;
WILDER, RL ;
HUNDER, GG .
ARTHRITIS AND RHEUMATISM, 1988, 31 (03) :315-324
[3]   Clustering of non-major histocompatibility complex susceptibility candidate loci in human autoimmune diseases [J].
Becker, KG ;
Simon, RM ;
Bailey-Wilson, JE ;
Freidlin, B ;
Biddison, WE ;
McFarland, HF ;
Trent, JM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (17) :9979-9984
[4]   A missense single-nucleotide polymorphism in a gene encoding a protein tyrosine phosphatase (PTPN22) is associated with rheumatoid arthritis [J].
Begovich, AB ;
Carlton, VEH ;
Honigberg, LA ;
Schrodi, SJ ;
Chokkalingam, AP ;
Alexander, HC ;
Ardlie, KG ;
Huang, QQ ;
Smith, AM ;
Spoerke, JM ;
Conn, MT ;
Chang, M ;
Chang, SYP ;
Saiki, RK ;
Catanese, JJ ;
Leong, DU ;
Garcia, VE ;
McAllister, LB ;
Jeffery, DA ;
Lee, AT ;
Batliwalla, F ;
Remmers, E ;
Criswell, LA ;
Seldin, MF ;
Kastner, DL ;
Amos, CI ;
Sninsky, JJ ;
Gregersen, PK .
AMERICAN JOURNAL OF HUMAN GENETICS, 2004, 75 (02) :330-337
[5]   A large-scale genetic association study confirms IL12B and leads to the identification of IL23R as psoriasis-risk genes [J].
Cargill, Michele ;
Schrodi, Steven J. ;
Chang, Monica ;
Garcia, Veronica E. ;
Brandon, Rhonda ;
Callis, Kristina P. ;
Matsunami, Nori ;
Ardlie, Kristin G. ;
Civello, Daniel ;
Catanese, Joseph J. ;
Leong, Diane U. ;
Panko, Jackie M. ;
McAllister, Linda B. ;
Hansen, Christopher B. ;
Papenfuss, Jason ;
Prescott, Stephen M. ;
White, Thomas J. ;
Leppert, Mark F. ;
Krueger, Gerald G. ;
Begovich, Ann B. .
AMERICAN JOURNAL OF HUMAN GENETICS, 2007, 80 (02) :273-290
[6]   Effector function of type II collagen-stimulated T cells from rheumatoid arthritis patients - Cross-talk between T cells and synovial fibroblasts [J].
Cho, ML ;
Yoon, CH ;
Hwang, SY ;
Park, MK ;
Min, SY ;
Lee, SH ;
Park, SH ;
Kim, HY .
ARTHRITIS AND RHEUMATISM, 2004, 50 (03) :776-784
[7]   New susceptibility locus for rheumatoid arthritis suggested by a genome-wide linkage study [J].
Cornelis, F ;
Faure, S ;
Martinez, M ;
Prud'Homme, JF ;
Fritz, P ;
Dib, C ;
Alves, H ;
Barrera, P ;
De Vries, N ;
Balsa, A ;
Pascual-Salcedo, D ;
Maenaut, K ;
Westhovens, R ;
Migliorini, P ;
Tran, TH ;
Delaye, A ;
Prince, N ;
Lefevre, C ;
Thomas, G ;
Poirier, M ;
Soubigou, S ;
Alibert, O ;
Lasbleiz, S ;
Fouix, S ;
Bouchier, C ;
Lioté, F ;
Loste, MN ;
Lepage, V ;
Charron, D ;
Gyapay, G ;
Lopes-Vaz, A ;
Kuntz, D ;
Bardin, T ;
Weissenbach, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (18) :10746-10750
[8]   A genome-wide association study identifies IL23R as an inflammatory bowel disease gene [J].
Duerr, Richard H. ;
Taylor, Kent D. ;
Brant, Steven R. ;
Rioux, John D. ;
Silverberg, Mark S. ;
Daly, Mark J. ;
Steinhart, A. Hillary ;
Abraham, Clara ;
Regueiro, Miguel ;
Griffiths, Anne ;
Dassopoulos, Themistocles ;
Bitton, Alain ;
Yang, Huiying ;
Targan, Stephan ;
Datta, Lisa Wu ;
Kistner, Emily O. ;
Schumm, L. Philip ;
Lee, Annette T. ;
Gregersen, Peter K. ;
Barmada, M. Michael ;
Rotter, Jerome I. ;
Nicolae, Dan L. ;
Cho, Judy H. .
SCIENCE, 2006, 314 (5804) :1461-1463
[9]   Evolving concepts of rheumatoid arthritis [J].
Firestein, GS .
NATURE, 2003, 423 (6937) :356-361
[10]   Autoimmune inflammation from the Th17 perspective [J].
Furuzawa-Carballeda, Janette ;
Vargas-Rojas, Maria Ines ;
Cabral, Antonio R. .
AUTOIMMUNITY REVIEWS, 2007, 6 (03) :169-175