AI Article Synopsis

  • The study investigates potential adverse reactions and lung disease linked to medications for systemic juvenile idiopathic arthritis (JIA), focusing on the role of HLA-DRB1*15 as a risk factor.
  • HLA typing in 23 subjects revealed that 74% carried the DRB1*15 gene, with all seven patients who developed systemic JIA-related lung disease (JIA-LD) also carrying this allele.
  • High rates of eosinophilia (39%) were found among patients, which correlated with adverse drug reactions and signals of macrophage activation syndrome, highlighting the need for close monitoring in this patient population.

Article Abstract

Objective: Concern exists that medications used to treat patients with systemic juvenile idiopathic arthritis (JIA), particularly interleukin (IL)-1 and IL-6 blocking agents, might be causing adverse drug reactions and lung disease (systemic JIA-LD). Carriage of HLA-DRB1*15 has been reported as a risk factor for adverse drug reactions among patients with systemic JIA. We performed a retrospective chart review to evaluate these factors at our center.

Methods: We reviewed the records of 86 subjects with systemic JIA followed for at least 6 months between 1996 and 2022. HLA typing was performed in 23 of the subjects. We compared characteristics of patients with or without eosinophilia. Among patients with HLA typing, we compared clinical characteristics of subjects with or without DRB1*15 and with or without systemic JIA-LD.

Results: Among the 23 patients with HLA typing, 74% carried DRB1*15, and 63% of patients without systemic JIA-LD carried DRB1*15. Seven subjects had systemic JIA-LD, all of whom carried DRB1*15. Patients with systemic JIA-LD were younger at the time of diagnosis and more likely to have had macrophage activation syndrome. Exposure to IL-1 and IL-6 blockers was common, occurring in 95% of patients. Eosinophilia occurred in 39% of patients with systemic JIA, often before IL-1 or IL-6 blockade. Eosinophilia was associated with adverse drug reactions and macrophage activation syndrome. There was 1 death, unrelated to active systemic JIA disease.

Conclusion: Carriage of DRB1*15 was more common in this cohort of patients with systemic JIA than in the general population. Eosinophilia and systemic JIA-LD were more common among patients with severe systemic JIA complicated by macrophage activation syndrome.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10524250PMC
http://dx.doi.org/10.1002/acr.25132DOI Listing

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