QT-interval parameters are increased in systemic lupus erythematosus patients

C R L Cardoso1, M A O Sales, J A S Papi

  • 1Department of Internal Medicine, Clementino Fraga Filho University Hospital, Medical School, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil. claudiacardoso@hucff.ufrj.br

Lupus
|November 24, 2005
PubMed

Insights

Systemic lupus erythematosus (SLE) patients exhibit prolonged QT-interval parameters, indicating heightened cardiovascular risk. These findings suggest potential subclinical atherosclerotic cardiovascular disease in SLE patients.

Area of Science:

  • Cardiology
  • Rheumatology
  • Electrocardiography

Background:

  • Systemic lupus erythematosus (SLE) is associated with increased cardiovascular morbidity and mortality.
  • QT-interval parameters are recognized markers of cardiovascular risk.
  • Previous evaluations of QT-interval parameters in SLE patients are lacking.

Purpose of the Study:

  • To evaluate QT-interval parameters (QTcmax and QTd) in female SLE outpatients.
  • To compare these parameters with age- and BMI-matched healthy controls.
  • To identify factors associated with QT-interval prolongation in SLE.

Main Methods:

  • Standard 12-lead ECGs were performed on 140 female SLE patients and 37 controls.
  • QT interval was measured, and heart rate-corrected maximum QT-interval duration (QTcmax) and QT-interval dispersion (QTd) were calculated.
  • Clinical data, cardiovascular risk factors, lupus disease activity, and damage were recorded.

Main Results:

  • SLE patients demonstrated significantly increased QTcmax and QTd compared to controls (P < 0.001 for both).
  • These differences remained significant even after excluding patients with hypertension, diabetes, or ECG abnormalities (P = 0.041 for QTcmax, P = 0.001 for QTd).
  • ECG-LVH, ST-T abnormalities, and left atrial enlargement were associated with QTcmax; age, ECG-LVH, and ST-T abnormalities were associated with QTd.

Conclusions:

  • SLE patients exhibit prolonged QT-interval parameters, suggesting an elevated cardiovascular risk.
  • This prolongation may be attributed to subclinical atherosclerotic cardiovascular disease in SLE.
  • QT-interval parameters warrant further investigation as potential biomarkers for cardiovascular risk in SLE.