Prevalence of cerebral microemboli in systemic lupus erythematosus: transcranial Doppler

J Kron1, U M Hamper, M Petri

  • 1Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA.

Insights

Microemboli detected by transcranial Doppler (TCD) in patients with systemic lupus erythematosus (SLE) occurred in 9.8% of cases. These events were linked to valve surgery and disease activity, not traditional stroke factors.

Area of Science:

  • Neurology
  • Rheumatology
  • Vascular Medicine

Background:

  • Systemic lupus erythematosus (SLE) is associated with an increased risk of cerebrovascular events.
  • Identifying predictors of stroke in SLE patients is crucial for risk stratification.
  • Transcranial Doppler (TCD) can detect microembolic signals (MES) as indicators of embolic activity.

Purpose of the Study:

  • To investigate the prevalence of microemboli using TCD in patients diagnosed with SLE.
  • To identify potential predictors associated with the presence of TCD-detected microemboli in this cohort.

Main Methods:

  • A cohort of 167 patients with SLE underwent TCD examinations.
  • Microembolic events were identified and quantified during TCD testing.
  • Statistical analysis was performed to determine predictors, including valve surgery history, SLE Disease Activity Index (SLEDAI), antiphospholipid antibodies, and carotid plaque presence.

Main Results:

  • Microembolic events were detected in 15 out of 153 (9.8%) SLE patients who completed TCD.
  • Predictors for TCD microemboli included prior valve repair or replacement (p < 0.0001) and a higher SLEDAI score (p = 0.07).
  • No significant association was found between TCD microemboli and antiphospholipid antibodies or carotid atherosclerotic plaque.

Conclusions:

  • TCD-detected microemboli may serve as a noninvasive marker for stroke risk assessment in SLE patients.
  • These microembolic events in SLE appear unrelated to conventional stroke risk factors.
  • Further longitudinal studies are warranted to establish the predictive value of TCD microemboli for future stroke events in SLE.
Abstract