PLoS ONE (Jan 2013)

Epistatic interaction between BANK1 and BLK in rheumatoid arthritis: results from a large trans-ethnic meta-analysis.

  • Emmanuelle Génin,
  • Baptiste Coustet,
  • Yannick Allanore,
  • Ikue Ito,
  • Maria Teruel,
  • Arnaud Constantin,
  • Thierry Schaeverbeke,
  • Adeline Ruyssen-Witrand,
  • Shigeto Tohma,
  • Alain Cantagrel,
  • Olivier Vittecoq,
  • Thomas Barnetche,
  • Xavier Le Loët,
  • Patrice Fardellone,
  • Hiroshi Furukawa,
  • Olivier Meyer,
  • Benjamin Fernández-Gutiérrez,
  • Alejandro Balsa,
  • Miguel A González-Gay,
  • Gilles Chiocchia,
  • Naoyuki Tsuchiya,
  • Javier Martin,
  • Philippe Dieudé

DOI
https://doi.org/10.1371/journal.pone.0061044
Journal volume & issue
Vol. 8, no. 4
p. e61044

Abstract

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BACKGROUND: BANK1 and BLK belong to the pleiotropic autoimmune genes; recently, epistasis between BANK1 and BLK was detected in systemic lupus erythematosus. Although BLK has been reproducibly identified as a risk factor in rheumatoid arthritis (RA), reports are conflicting about the contribution of BANK1 to RA susceptibility. To ascertain the real impact of BANK1 on RA genetic susceptibility, we performed a large meta-analysis including our original data and tested for an epistatic interaction between BANK1 and BLK in RA susceptibility. PATIENTS AND METHODS: We investigated data for 1,915 RA patients and 1,915 ethnically matched healthy controls genotyped for BANK1 rs10516487 and rs3733197 and BLK rs13277113. The association of each SNP and RA was tested by logistic regression. Multivariate analysis was then used with an interaction term to test for an epistatic interaction between the SNPs in the 2 genes. RESULTS: None of the SNPs tested individually was significantly associated with RA in the genotyped samples. However, we detected an epistatic interaction between BANK1 rs3733197 and BLK rs13277113 (P(interaction) = 0.037). In individuals carrying the BLK rs13277113 GG genotype, presence of the BANK1 rs3733197 G allele increased the risk of RA (odds ratio 1.21 [95% confidence interval 1.04-1.41], P = 0.015. Combining our results with those of all other studies in a large trans-ethnic meta-analysis revealed an association of the BANK1 rs3733197 G allele and RA (1.11 [1.02-1.21], P = 0.012). CONCLUSION: This study confirms BANK1 as an RA susceptibility gene and for the first time provides evidence for epistasis between BANK1 and BLK in RA. Our results illustrate the concept of pleiotropic epistatic interaction, suggesting that BANK1 and BLK might play a role in RA pathogenesis.