Genetic Variations in Pattern Recognition Receptor Loci Are Associated with Anti-TNF Response in Patients with Rheumatoid Arthritis

PLoS One. 2015 Oct 6;10(10):e0139781. doi: 10.1371/journal.pone.0139781. eCollection 2015.

Abstract

Objectives: To determine whether genetic variation within genes related to the Toll-like receptor, inflammasome and interferon-γ pathways contributes to the differences in treatment response to tumour necrosis factor inhibitors (anti-TNF) in patients with rheumatoid arthritis (RA).

Methods: In a retrospective case-case study, we assessed 23 functional single nucleotide polymorphisms (SNPs) in 15 genes. We included 538 anti-TNF naïve Danish RA patients from the nationwide DANBIO database. Multivariable logistic regression analyses were performed to detect associations (p-value<0.05) between genotypes and European League Against Rheumatism (EULAR) treatment responses. False Discovery Rate corrections for multiple testing (q-value) and stratified analyses were performed to investigate association with individual therapies and IgM-rheumatoid factor (RF) status.

Results: Six of twenty successfully genotyped polymorphisms were nominally associated with EULAR treatment response. Three of these were in weak to moderate linkage disequilibrium with polymorphisms previously reported associated with anti-TNF treatment response. TLR5(rs5744174) variant allele carriers (odds ratio(OR) = 1.7(1.1-2.5),p = 0.010,q = 0.46) and TLR1(rs4833095) homozygous variant carriers (OR = 2.8(1.1-7.4),p = 0.037,q = 0.46) had higher odds for a positive treatment response. NLRP3(rs10754558) variant allele carriers (odds ratio(OR) = 0.6(0.4-1.0),p = 0.045,q = 0.46) were more likely to have a negative treatment response. The association in TLR5(rs5744174) remained significant after correction for multiple comparisons among patients negative for RF (OR = 6.2(2.4-16.3),p = 0.0002,q = 0.024). No other association withstood correction for multiple testing. Post hoc analyses showed that change in Patient Global score on a visual analogue scale (VAS) and change in pain VAS were the main factors responsible for the association.

Conclusions: We reproduced previously reported associations between genetic variation in the TLR10/1/6 gene cluster, TLR5, and NLRP3 loci and response to anti-TNF treatment in RA. Changes in VAS pain and patient global scores were the main contributors to the association found for TLR5. Furthermore, we identified other candidate genes that require replication in independent cohorts.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adalimumab / therapeutic use
  • Adaptor Proteins, Signal Transducing / genetics*
  • Adult
  • Aged
  • Alleles
  • Antirheumatic Agents / therapeutic use*
  • Apoptosis Regulatory Proteins / genetics*
  • Arthritis, Rheumatoid / drug therapy
  • Arthritis, Rheumatoid / genetics*
  • Etanercept / therapeutic use
  • Female
  • Gene Frequency
  • Genetic Association Studies
  • Genetic Loci
  • Humans
  • Inflammasomes / genetics
  • Infliximab / therapeutic use
  • Interferon-gamma / genetics
  • Linkage Disequilibrium
  • Male
  • Middle Aged
  • NLR Proteins
  • Polymorphism, Single Nucleotide*
  • Retrospective Studies
  • Toll-Like Receptors / genetics*
  • Treatment Outcome

Substances

  • Adaptor Proteins, Signal Transducing
  • Antirheumatic Agents
  • Apoptosis Regulatory Proteins
  • Inflammasomes
  • NLR Proteins
  • NLRP1 protein, human
  • Toll-Like Receptors
  • Interferon-gamma
  • Infliximab
  • Adalimumab
  • Etanercept

Grants and funding

This study was supported by the Danish Rheumatism Association, R95-A1913/R99-A1923 (www.gigtforeningen.dk), Region of Southern Denmark’s PhD Fund, 12/7725 (www.regionsyddanmark.dk) and the Department of Rheumatology, Frederiksberg Hospital (www.frederiksberghospital.dk). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.