Fine-mapping the MHC locus in juvenile idiopathic arthritis (JIA) reveals genetic heterogeneity corresponding to distinct adult inflammatory arthritic diseases.

Research output: Contribution to journalArticle

  • External authors:
  • Anne Hinks
  • Joanna Cobb
  • H. C. Ainsworth
  • M. C. Marion
  • M. E. Comeau
  • B. Han
  • M. L. Becker
  • J. F. Bohnsack
  • P. I. W. de Bakker
  • J. P. Haas
  • M. Hazen
  • D. J. Lovell
  • P. A. Nigrovic
  • E. Nordal
  • M. Punnaro
  • A. M. Rosenberg
  • M. Rygg
  • C. A. Wise
  • V. Videm
  • L. R. Wedderburn
  • R. S. M. Yeung
  • S. Prahalad
  • C. D. Langefeld
  • Soumya Raychaudhuri
  • S. D. Thompson

Abstract

Objectives:
Juvenile idiopathic arthritis (JIA) is a heterogeneous group of diseases, comprising seven categories. Genetic data could potentially be used to help redefine JIA categories and improve the current classification system. The human leukocyte antigen (HLA) region is strongly associated with JIA. Fine-mapping of the region was performed to look for similarities and differences in HLA associations between the JIA categories and define correspondences with adult inflammatory arthritides.

Methods:
Dense genotype data from the HLA region, from the Immunochip array for 5,043 JIA cases and 14,390 controls, was used to impute SNPs, HLA classical alleles and amino acids. Bivariate analysis was performed to investigate genetic correlation between the JIA categories. Conditional analysis was used to identify additional effects within the region. Comparison of the findings with those in adult inflammatory arthritic diseases was performed.

Results
We identified category-specific associations and have demonstrated for the first time that rheumatoid factor negative polyarticular JIA and oligoarticular JIA are genetically similar in their HLA associations. We also observe that each JIA category potentially has an adult counterpart. The RF-positive polyarthritis association at HLA-DRB1 amino acid at position 13 mirrors the association in adult seropositive rheumatoid arthritis (RA). Interestingly, the combined oligoarthritis and RF-negative polyarthritis dataset shares the same association with adult seronegative RA.

Conclusions
The findings suggest the value of using genetic data in helping to classify the categories of this heterogeneous disease. Mapping JIA categories to adult counterparts could enable shared knowledge of disease pathogenesis and etiology and facilitate transition from paediatric to adult services.

Bibliographical metadata

Original languageEnglish
Pages (from-to)765–772
JournalAnnals of the rheumatic diseases
Volume76
Issue number4
Early online date20 Dec 2016
DOIs
Publication statusPublished - Apr 2017

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