# Advancing Juvenile Spondyloarthritis: Closing Knowledge Gaps with New Axial JSpA Classification Criteria

**Authors:** Brittney N. Newby, Pamela F. Weiss

PMC · DOI: 10.1007/s11926-025-01206-8 · 2025-11-18

## TL;DR

This paper discusses new classification criteria for axial juvenile spondyloarthritis to improve diagnosis and treatment in children.

## Contribution

The paper introduces newly validated pediatric-specific axial JSpA classification criteria to address diagnostic gaps.

## Key findings

- Fewer than 20% of children with JSpA achieve remission within five years of diagnosis.
- Axial JSpA requires distinct management as it does not respond to conventional therapies like methotrexate.
- New 2024 classification criteria include MRI findings, pain patterns, and genetic associations for axial JSpA.

## Abstract

Until recently, the absence of validated, pediatric-specific classification criteria for juvenile spondyloarthritis (JSpA) limited targeted clinical trials evaluating treatment efficacy and advancements in understanding the natural history in pediatric-onset disease. There is an urgent need for efficacy and effectiveness studies in this understudied group.

Most children with JSpA continue to experience disease activity despite current therapies and generally have worse outcomes than those with other juvenile arthritis forms. Fewer than 20% achieve remission within five years of diagnosis. Axial involvement is a distinct manifestation warranting separate study and management, as it does not respond to conventional agents like methotrexate used for peripheral arthritis. Comparative effectiveness data are lacking, and no medications are FDA-approved specifically for “juvenile spondyloarthritis” or “juvenile ankylosing spondylitis.” The only FDA-approved therapy for enthesitis-related arthritis (ERA) is secukinumab. In 2024, pediatric classification criteria for axial disease in JSpA were published. These criteria include seven domains: MRI inflammation, MRI structural lesions, pain chronicity, pain pattern, pain location, stiffness, and genetic association. Imaging evidence of axial disease is necessary but not sufficient for classification.

This review provides an overview of JSpA epidemiology, current and emerging classification criteria, and highlights the key features of the newly validated pediatric axial JSpA classification criteria.

## Linked entities

- **Chemicals:** methotrexate (PubChem CID 4112)
- **Diseases:** juvenile spondyloarthritis (MONDO:0043377), ankylosing spondylitis (MONDO:0005306), enthesitis-related arthritis (MONDO:0019437)

## Full-text entities

- **Diseases:** JSpA (MESH:D013167), axial disease (MESH:C537791), peripheral arthritis (MESH:D001168), ERA (MESH:D001171), inflammation (MESH:D007249), pain (MESH:D010146)
- **Chemicals:** methotrexate (MESH:D008727), secukinumab (MESH:C555450)

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12627101/full.md

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Source: https://tomesphere.com/paper/PMC12627101