Risk factors associated with disease relapse in healing/healed arterial injury and biopsy-proven giant cell arteritis

Wei Sim1, Jack Mouhanna2, Danah Albreiki1

  • 1Department of Ophthalmology, University of Ottawa, Ottawa, ON, Canada.

Insights

Giant cell arteritis (GCA) relapse characteristics were compared to healing/healed (HH) arterial injury. Large-vessel vasculitis, like aortitis, independently predicts relapse in GCA patients, suggesting similar clinical management for both groups.

Area of Science:

  • Rheumatology
  • Immunology
  • Vascular Medicine

Background:

  • Giant cell arteritis (GCA) is a systemic vasculitis primarily affecting large arteries.
  • Temporal artery biopsy (TAB) is crucial for diagnosis, distinguishing active GCA from healing/healed (HH) arterial injury.
  • Understanding relapse patterns in both GCA and HH groups is essential for effective patient management.

Purpose of the Study:

  • To compare relapse characteristics in patients with biopsy-proven GCA versus those with HH arterial injury on TAB.
  • To identify risk factors associated with symptomatic or biochemical relapses in these patient cohorts.

Main Methods:

  • Retrospective cohort study involving 135 patients with GCA-positive or HH arterial injury on TAB.
  • Minimum 12-month follow-up period (January 2009 - December 2018).
  • Evaluation of clinical characteristics and serological markers as potential relapse risk factors.

Main Results:

  • Relapse rates were similar between HH (16.9%) and GCA-positive (25.7%) groups (p=0.21).
  • Aortitis was significantly associated with relapse and earlier relapse rates in GCA-positive patients (p=0.007).
  • Aortitis and jaw claudication were independent risk factors for relapse in GCA; aortitis and aortic aneurysm were associated with relapse in HH patients.

Conclusions:

  • Large-vessel vasculitis, including aortitis, is linked to disease relapse in both GCA and HH biopsy groups.
  • Similar relapse characteristics suggest clinicians can manage both patient groups similarly based on clinical history.
  • Management decisions should not solely rely on TAB pathology findings but integrate clinical context.
Abstract