Genome-wide association analysis of anti-TNF drug response in patients with rheumatoid arthritis

被引:87
作者
Mirkov, Masa Umicevic [1 ]
Cui, Jing [2 ,3 ]
Vermeulen, Sita H. [1 ,4 ]
Stahl, Eli A.
Toonen, Erik J. M. [5 ]
Makkinje, Remco R.
Lee, Annette T. [6 ]
Huizinga, Tom W. J. [7 ]
Allaart, Renee [7 ]
Barton, Anne [8 ,9 ]
Mariette, Xavier [10 ]
Miceli, Corinne Richard [10 ]
Criswell, Lindsey A. [11 ]
Tak, Paul P. [12 ,13 ]
de Vries, Niek [12 ,13 ]
Saevarsdottir, Saedis [14 ]
Padyukov, Leonid [14 ]
Bridges, S. Louis [15 ]
van Schaardenburg, Dirk-Jan [16 ,17 ]
Jansen, Tim L. [18 ]
Dutmer, Ellen A. J. [19 ]
de laar, Mart A. F. J. van [20 ]
Barrera, Pilar [18 ]
Radstake, Timothy R. D. J. [21 ,22 ]
van Riel, Piet L. C. M. [18 ]
Scheffer, Hans [1 ]
Franke, Barbara [1 ,23 ]
Brunner, Han G. [1 ]
Plenge, Robert M. [2 ,3 ]
Gregersen, Peter K. [6 ]
Guchelaar, Henk-Jan [24 ]
Coenen, Marieke J. H. [1 ]
机构
[1] Radboud Univ Nijmegen, Dept Human Genet, Med Ctr, NL-6500 HB Nijmegen, Netherlands
[2] Brigham & Womens Hosp, Dept Rheumatol Immunol & Allergy, Boston, MA 02115 USA
[3] Broad Inst, Boston, MA 02115 USA
[4] Radboud Univ Nijmegen, Med Ctr, Dept Epidemiol Biostat & HTA, NL-6500 HB Nijmegen, Netherlands
[5] Radboud Univ Nijmegen, Med Ctr, Dept Med, NL-6500 HB Nijmegen, Netherlands
[6] Feinstein Inst Med Res, North Shore LIJ, Robert S Boas Ctr Genom & Human Genet, Manhasset, NY USA
[7] Leiden Univ, Dept Rheumatol, Med Ctr, Leiden, Netherlands
[8] Univ Manchester, Arthritis Res UK Epidemiol Unit, Manchester Acad Hlth Sci, Manchester, Lancs, England
[9] Cent Manchester Univ Hosp NHS Fdn Trust, Manchester Acad Hlth Sci Ctr, NIHR Manchester Musculoskeletal Biomed Res Unit, Manchester, Lancs, England
[10] Univ Paris 11, Dept Rheumatol, Hop Univ Paris Sud, AP HP,INSERM U1012, Paris, France
[11] Univ Calif San Francisco, Dept Med, Rosalind Russell Med Res Ctr Arthrit, San Francisco, CA USA
[12] AMC Univ Amsterdam, Dept Clin Immunol & Rheumatol, Amsterdam, Netherlands
[13] GlaxoSmithKline, Stevenage, Herts, England
[14] Karolinska Univ Hosp, Karolinska Inst, Dept Med, Rheumatol Unit, Stockholm, Sweden
[15] Univ Alabama Birmingham, Div Clin Immunol & Rheumatol, Birmingham, AL 35294 USA
[16] Jan van Breemen Inst, Reade Ctr Rehabil & Rheumatol, Dept Rheumatol, Amsterdam, Netherlands
[17] Vrije Univ Amsterdam, Med Ctr, Dept Rheumatol, NL-17DEPART Amsterdam, Netherlands
[18] Radboud Univ Nijmegen, Med Ctr, Dept Rheumatol, NL-6500 HB Nijmegen, Netherlands
[19] Gelderse Vallei Hosp, Dept Rheumatol, Ede, Netherlands
[20] Univ Twente & Med Spectrum Twente, Arthrit Ctr Twente, Dept Rheumatol & Clin Immunol, Enschede, Netherlands
[21] Univ Med Ctr Utrecht, Dept Rheumatol & Clin Immunol, Utrecht, Netherlands
[22] Wilhemina Childrens Hosp, Utrecht, Netherlands
[23] Radboud Univ Nijmegen, Med Ctr, Dept Psychiat, NL-6500 HB Nijmegen, Netherlands
[24] Leiden Univ, Med Ctr, Dept Clin Pharm & Toxicol, Leiden, Netherlands
关键词
Anti-TNF; Gene Polymorphism; Pharmacogenetics; Rheumatoid Arthritis; RECEIVING CONCOMITANT METHOTREXATE; ALPHA MONOCLONAL-ANTIBODY; CLINICAL-PRACTICE; THERAPY; POLYMORPHISMS; TRIAL; LOCI; INFLIXIMAB; REPLICATION; ETANERCEPT;
D O I
10.1136/annrheumdis-2012-202405
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Treatment strategies blocking tumour necrosis factor (anti-TNF) have proven very successful in patients with rheumatoid arthritis (RA). However, a significant subset of patients does not respond for unknown reasons. Currently, there are no means of identifying these patients before treatment. This study was aimed at identifying genetic factors predicting anti-TNF treatment outcome in patients with RA using a genome-wide association approach. Methods We conducted a multistage, genome-wide association study with a primary analysis of 2557253 single-nucleotide polymorphisms (SNPs) in 882 patients with RA receiving anti-TNF therapy included through the Dutch Rheumatoid Arthritis Monitoring (DREAM) registry and the database of Apotheekzorg. Linear regression analysis of changes in the Disease Activity Score in 28 joints after 14weeks of treatment was performed using an additive model. Markers with p<10(-3) were selected for replication in 1821 patients from three independent cohorts. Pathway analysis including all SNPs with p<10(-3) was performed using Ingenuity. Results 772 markers showed evidence of association with treatment outcome in the initial stage. Eight genetic loci showed improved p value in the overall meta-analysis compared with the first stage, three of which (rs1568885, rs1813443 and rs4411591) showed directional consistency over all four cohorts studied. We were unable to replicate markers previously reported to be associated with anti-TNF outcome. Network analysis indicated strong involvement of biological processes underlying inflammatory response and cell morphology. Conclusions Using a multistage strategy, we have identified eight genetic loci associated with response to anti-TNF treatment. Further studies are required to validate these findings in additional patient collections.
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收藏
页码:1375 / 1381
页数:7
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