Infection is associated with increased risk of MPO- but not PR3-ANCA-associated vasculitis

Jens Rathmann1, Pavlos Stamatis1, Göran Jönsson2

  • 1Department of Clinical Sciences, Rheumatology.

Abstract

Insights

Prior infections, particularly respiratory ones, are linked to developing ANCA-associated vasculitis (AAV), especially MPO-ANCA types. Infections also correlate with increased disease activity at diagnosis.

Area of Science:

  • Immunology
  • Rheumatology
  • Epidemiology

Background:

  • ANCA-associated vasculitis (AAV) is a group of rare autoimmune diseases.
  • The role of prior infections in AAV development and disease characteristics requires further investigation.

Purpose of the Study:

  • To investigate the association between prior infections and the development of AAV.
  • To determine if prior infections influence AAV disease characteristics and patient outcomes.

Main Methods:

  • A case-control study identified incident AAV cases in Sweden (2000-2016) and matched them with population controls.
  • Infections occurring before the AAV diagnosis date were identified using administrative databases.
  • Conditional logistic regression was used to calculate odds ratios (OR) for AAV development, and analyses explored associations with disease characteristics and outcomes.

Main Results:

  • 54% of AAV patients had a prior infection compared to 48% of controls.
  • Infections of the upper respiratory tract (OR 1.57) and pneumonia (OR 1.68) were associated with increased AAV risk.
  • This association was significant for myeloperoxidase-ANCA (MPO-ANCA) vasculitis (OR 1.99) but not proteinase 3-ANCA (PR3-ANCA) vasculitis.
  • Patients with prior infections exhibited higher disease activity at AAV diagnosis.

Conclusions:

  • Respiratory tract infections are associated with the development of MPO-ANCA vasculitis.
  • Prior infections are linked to heightened disease activity at the time of AAV diagnosis.
  • No significant differences in disease characteristics, comorbidities, or outcomes were observed based on prior infection status.

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