Differences in clinical features between axial psoriatic arthritis and axial spondyloarthritis: a systematic review and meta-analysis of observational studies - Scorecard - MDSpire

Differences in clinical features between axial psoriatic arthritis and axial spondyloarthritis: a systematic review and meta-analysis of observational studies

  • By

  • Zhihao Qiu

  • Zijie Chen

  • Zhe Yang

  • Ruibo Xia

  • Weikai Chen

  • Yuwei Zhu

  • Weijie Wang

  • Zhengfu Li

  • Kepeng Yang

  • June 22, 2026

  • 0 min

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Clinical Scorecard: Comparative Analysis of Clinical Characteristics in Axial Psoriatic Arthritis and Axial Spondyloarthritis: A Systematic Review and Meta-Analysis of Observational Research

At a Glance

CategoryDetail
ConditionAxial Psoriatic Arthritis and Axial Spondyloarthritis
Key MechanismsHLA-B27 positivity and IL-23/IL-17 axis activation
Target PopulationPatients with axial involvement in Psoriatic Arthritis and Axial Spondyloarthritis
Care SettingObservational studies and clinical trials

Key Highlights

  • No significant differences in disease activity scores between ax-PsA and ax-SpA.
  • ax-PsA associated with lower HLA-B27 positivity compared to ax-SpA.
  • Subgroup analyses show ax-PsA has modestly better BASFI scores than ax-SpA.
  • IL-23 inhibitors may improve axial symptoms in ax-PsA patients.
  • Clinical differentiation should include HLA-B27 testing and imaging.

Guideline-Based Recommendations

Diagnosis

  • Incorporate HLA-B27 testing for clinical differentiation.

Management

  • Consider IL-23 inhibitors for improving axial symptoms in ax-PsA.

Monitoring & Follow-up

  • Evaluate disease activity scores and imaging findings.

Risks

  • Limited efficacy of biologics targeting downstream inflammatory cytokines in ax-SpA.

Patient & Prescribing Data

Patients with axial Psoriatic Arthritis and Axial Spondyloarthritis.

IL-23 inhibitors may be more effective for ax-PsA than for ax-SpA.

Clinical Best Practices

  • Utilize standardized diagnostic criteria where available.
  • Conduct thorough assessments of disease activity and functional outcomes.
  • Consider regional variations in HLA-B27 positivity in clinical evaluations.

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