4.5 Article

Inflammatory Bowel Disease in Children With Systemic Juvenile Idiopathic Arthritis

Journal

JOURNAL OF RHEUMATOLOGY
Volume 48, Issue 4, Pages 567-574

Publisher

J RHEUMATOL PUBL CO
DOI: 10.3899/jrheum.200230

Keywords

autoinflammation; cytokine inhibitors; inflammatory bowel disease; pediatric rheumatology; systemic juvenile idiopathic arthritis

Categories

Funding

  1. National Institutes of Health (NIH) [T32AR050942-14]
  2. Tashia and John Morgridge Endowed Postdoctoral Fellow Clinical Trainee Award, Stanford Maternal & Child Health Research Institute
  3. The Marcus Foundation Inc., Atlanta, Georgia
  4. Feldman Family Foundation Visiting Professors Program, Stanford University School of Medicine
  5. Arthritis Foundation Great Western Region Center of Excellence for Arthritis
  6. The Lucile Packard Foundation for Children's Health
  7. National Institute of Arthritis and Musculoskeletal and Skin Diseases of the NIH [RC2AR058934]

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The occurrence of inflammatory bowel disease in the setting of systemic juvenile idiopathic arthritis is rare, with patients showing favorable response to tumor necrosis factor-alpha inhibitors.
Objective. The incidence of inflammatory bowel disease (IBD) in juvenile idiopathic arthritis (JIA) is higher than in the general pediatric population. However, reports of IBD in the systemic JIA (sJIA) subtype are limited. We sought to characterize sJIA patients diagnosed with IBD and to identify potential contributing risk factors. Methods. Using an internationally distributed survey, we identified 16 patients with sJIA who were subsequently diagnosed with IBD (sJIA-IBD cohort). Five hundred twenty-two sJIA patients without IBD were identified from the CARRA Legacy Registry and served as the sJIA-only cohort for comparison. Differences in demographic, clinical characteristics, and therapy were assessed using chi-square test, Fisher exact test, t-test, and univariate and multivariate logistic regression, as appropriate. Results. Of the patients with sJIA-IBD, 75% had a persistent sJIA course and 25% had a history of macrophage activation syndrome. sJIA-IBD subjects were older at sJIA diagnosis, more often non-White, had a higher rate of IBD family history, and were more frequently treated with etanercept or canakinumab compared to sJIA-only subjects. Sixty-nine percent of sJIA-IBD patients successfully discontinued sJIA medications following IBD diagnosis, and sJIA symptoms resolved in 9 of 12 patients treated with tumor necrosis factor-alpha (TNF-alpha) inhibitors. Conclusion. IBD in the setting of sJIA is a rare occurrence. The favorable response of sJIA symptoms to therapeutic TNF-alpha inhibition suggests that the sJIA-IBD cohort may represent a mechanistically distinct sJIA subgroup. Our study highlights the importance of maintaining a high level of suspicion for IBD when gastrointestinal involvement occurs in patients with sJIA and the likely broad benefit of TNF-alpha inhibition in those cases.

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