The early cardiovascular changes in pediatric patients with systemic lupus erythematosus

Betul Sozeri1, Murat Deveci, Nida Dincel

  • 1Department of Pediatric Rheumatology, Faculty of Medicine, Ege University, Bornova, Izmir, Turkey. betulsozeri@yahoo.com

Insights

Pediatric patients with Systemic Lupus Erythematosus (SLE) exhibit early cardiovascular changes (CVCs) independent of traditional risk factors. These functional and morphological CVCs correlate with SLE disease activity, highlighting the need for early monitoring.

Area of Science:

  • Cardiovascular Medicine
  • Pediatric Rheumatology
  • Immunology

Background:

  • Systemic Lupus Erythematosus (SLE) is associated with increased cardiovascular morbidity and mortality.
  • Inflammatory and immune mechanisms in SLE contribute to atherosclerosis and cardiovascular changes (CVCs).
  • The presence and impact of CVCs in pediatric SLE patients require investigation.

Purpose of the Study:

  • To assess functional and morphological cardiovascular changes in pediatric SLE patients.
  • To determine if these changes are independent of traditional cardiovascular risk factors.
  • To explore the correlation between cardiovascular changes and SLE disease activity.

Main Methods:

  • Study included 51 pediatric SLE patients and 25 healthy controls.
  • Arterial stiffness assessed using carotid-femoral pulse wave velocity (PWVcf) and augmentation index (AIx).
  • Carotid intima-media thickness (cIMT) and left ventricular mass index (LVMi) were measured.

Main Results:

  • SLE patients showed significantly higher PWVcf, AIx, cIMT, and LVMi compared to controls.
  • These differences persisted despite similar exposure to traditional cardiovascular risk factors.
  • Cardiovascular parameters correlated significantly with SLE disease activity scores.

Conclusions:

  • Pediatric SLE patients exhibit early functional and morphological cardiovascular changes.
  • These changes are independent of traditional cardiovascular risk factors.
  • Cardiovascular changes in early-stage pediatric SLE correlate with disease activity.
Abstract

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