Management of Polyarticular Course Juvenile Idiopathic Arthritis and Temporomandibular Joint Arthritis: A Systematic

Kai Liang Teh1, Mariel B Valmonte2, Taqdees Khaliq3

  • 1Rheumatology and Immunology Service, KK Women's and Children's Hospital, Singapore, Singapore.

Insights

This systematic review provides evidence for managing juvenile idiopathic arthritis (JIA) in the Asia Pacific. It highlights methotrexate and biologics as effective treatments, with emerging support for JAK inhibitors and biosimilars.

Area of Science:

  • Rheumatology
  • Pediatric Rheumatology
  • Systematic Review & Meta-Analysis

Background:

  • Juvenile idiopathic arthritis (JIA) is a common chronic rheumatic disease requiring targeted management to prevent long-term disability.
  • Existing Western guidelines may not fully address Asia Pacific-specific factors like genetic variations and healthcare infrastructure.
  • This study focuses on polyarticular course JIA (pcJIA) and temporomandibular joint (TMJ) arthritis management.

Purpose of the Study:

  • To conduct a systematic literature review (SLR) and meta-analysis to inform the Asia Pacific League of Associations for Rheumatology (APLAR) recommendations.
  • To provide up-to-date evidence for managing pcJIA and TMJ arthritis within the Asia Pacific region.
  • To identify region-specific treatment strategies and evidence gaps.

Main Methods:

  • Systematic review adhering to PRISMA guidelines, searching multiple databases (MEDLINE, Embase, Web of Science, Scopus, CENTRAL) through January 2025.
  • Inclusion of studies on pharmacologic and non-pharmacologic treatments for pcJIA and TMJ involvement, excluding those in existing guidelines.
  • Quality and evidence certainty assessed using Cochrane Rob2 tool and GRADE approach; meta-analyses performed where applicable.

Main Results:

  • Methotrexate remains a cornerstone csDMARD, with subcutaneous administration potentially offering advantages.
  • Biological DMARDs (abatacept, tocilizumab) demonstrate good efficacy and safety; JAK inhibitors show emerging promise.
  • Biosimilars exhibited comparable efficacy and safety to originators in observational studies; limited evidence supports gradual medication tapering to reduce flares.

Conclusions:

  • The SLR provides crucial evidence for region-specific JIA clinical practice, supporting many global recommendations.
  • Significant evidence gaps persist in medication tapering, biosimilar utilization, TMJ management, and non-pharmacological therapies.
  • Findings will directly contribute to APLAR's forthcoming clinical practice guidelines for pcJIA and TMJ arthritis.
Abstract

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