Advancing the treatment of juvenile idiopathic arthritis

Treatment for juvenile idiopathic arthritis has undergone substantial changes in recent decades. These changes are partly due to the availability of new treatments, mainly biological agents, as well as developments in treatment strategies, including a focus on concepts such as treat-to-target. In addition, the creation of large paediatric research networks has improved patient access to, and design of, clinical trials for rare paediatric diseases. Although these advances have resulted in improvements in care for most patients with juvenile idiopathic arthritis, certain subgroups of patients continue to have a poor prognosis. Further research aims to identify patients in these subgroups early, to personalise their care, improve functional outcomes, and minimise long-term damage and harm. Optimising the duration of therapy for those individuals who require systemic immunosuppression is also of importance. Incorporation of novel biomarkers in combination with validated clinical measures in an effort to predict outcomes and target therapy accordingly is an exciting development.

Automated summary

Treatment for juvenile idiopathic arthritis has evolved significantly in recent years, with the availability of new therapies, development of treatment strategies, and establishment of research networks. While most patients have benefited from these advancements, certain subgroups still face poor outcomes. Future research aims to identify these patients early, personalize their care, and minimize long-term damage.