Serious infections in patients with myasthenia gravis: population-based cohort study

C D Kassardjian1, J Widdifield2,3,4, J M Paterson3,4

  • 1Division of Neurology, Department of Medicine, St Michael's Hospital, University of Toronto, Toronto, ON.

Abstract

Insights

Patients with myasthenia gravis (MG) face double the risk of serious infections compared to the general population. This increased risk, particularly for respiratory infections, requires consideration in treatment and prevention strategies.

Area of Science:

  • Neurology
  • Infectious Diseases
  • Epidemiology

Background:

  • Myasthenia gravis (MG) is an autoimmune disorder affecting neuromuscular junctions.
  • The risk of serious infections in MG patients is not fully characterized.
  • Understanding infection risk is crucial for managing MG patients.

Purpose of the Study:

  • To determine the frequency and risk of serious infections in patients diagnosed with myasthenia gravis (MG).
  • To compare infection rates in MG patients against age, sex, and area-matched general population controls.
  • To identify specific types of infections prevalent in the MG cohort.

Main Methods:

  • A population-based cohort study was conducted in Ontario, Canada.
  • Newly-diagnosed MG patients (n=3823) were compared to 1:4 matched controls (n=15,292).
  • Serious infections were identified via hospitalization or emergency department records; Cox regression analyzed adjusted hazard ratios.

Main Results:

  • MG patients had a significantly higher incidence of serious infections (33.4%) versus controls (19.4%).
  • Crude infection rates were doubled in MG patients (72.5 vs. 35.0 per 1000 person-years).
  • MG was associated with a 39% increased risk of serious infection (aHR, 1.39; 95% CI, 1.28-1.51), with respiratory infections being most common.

Conclusions:

  • Patients with myasthenia gravis have a substantially elevated risk of serious infections.
  • This heightened risk necessitates careful consideration in MG treatment selection and prophylaxis planning.
  • Further research is needed to differentiate infection risk attributed to MG versus its immunosuppressive treatments.

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