Vascular Reactivity of Adult-Onset Systemic Lupus Erythematosus Patients

Mohammad Adawi1,2, Tair Abu-Gabel1,2, Firas Sabbah1,2

  • 1Department of Rheumatology, Padeh Medical Center, Poriya, Israel.

Insights

Systemic lupus erythematosus (SLE) patients, particularly women, face higher cardiovascular disease (CVD) risks. This study found impaired endothelial function in adult-onset SLE females despite modern treatments, indicating a persistent CVD risk.

Area of Science:

  • Rheumatology and Immunology
  • Cardiology
  • Vascular Biology

Background:

  • Systemic lupus erythematosus (SLE) significantly increases cardiovascular disease (CVD) risk compared to the general population.
  • Women with SLE are disproportionately affected, often developing CVD at younger ages, including pre-menopause, unlike the general female population.

Purpose of the Study:

  • To assess endothelial function in adult-onset SLE female patients from Northern Israel.
  • To investigate if contemporary management strategies, including biological therapies, mitigate CVD risk in these patients.

Main Methods:

  • A prospective study involving 13 pre-menopausal females with adult-onset SLE (without renal involvement) and 11 age-matched healthy female controls.
  • Evaluation of clinical parameters (age, BMI, height), laboratory markers (CRP, hemoglobin), and vascular responsiveness (flow-mediated dilation percentage change [FMD%]).
  • Statistical comparison using the Student's t-test to identify significant differences between the SLE and control groups.

Main Results:

  • No significant differences were found in age, BMI, or hemoglobin levels between SLE patients and controls.
  • SLE patients exhibited significantly higher C-reactive protein (CRP) levels (P=0.001) and impaired vascular responsiveness (FMD%) (P=0.012).
  • A significant difference in height was also noted (P=0.009).

Conclusions:

  • Adult-onset SLE in females is associated with impaired endothelial function, a key indicator of cardiovascular risk.
  • Current treatment protocols, even those including biological agents, do not fully restore endothelial function in these patients.
  • This suggests a continued elevated CVD risk in pre-menopausal women with SLE, necessitating ongoing monitoring and potentially novel therapeutic approaches.
Abstract

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