Effects of belimumab on the lipid profile in systemic lupus erythematosus patients: an observational study

Di Liang1, Shimei Huang1, Rui Ding2

  • 1Department of Rheumatology, Zhongshan Hospital Xiamen University, School of Medicine, Xiamen University, Xiamen, Fujian, China.

Clinical Rheumatology
|June 14, 2024
PubMed

Insights

Belimumab treatment significantly increased high-density lipoprotein (HDL) cholesterol in systemic lupus erythematosus (SLE) patients. This improvement in HDL levels correlated with reduced disease activity and may help manage cardiovascular risk in SLE.

Area of Science:

  • Rheumatology and Immunology
  • Cardiovascular Risk Management in Autoimmune Diseases

Background:

  • Systemic lupus erythematosus (SLE) is associated with dyslipidemia and increased cardiovascular risk.
  • Belimumab, a biologic therapy, targets B-cell pathways in SLE management.
  • The impact of belimumab on lipid profiles in SLE patients requires further investigation.

Purpose of the Study:

  • To investigate the effects of belimumab on lipid profiles in patients with systemic lupus erythematosus (SLE).
  • To compare lipid profile changes in SLE patients treated with belimumab versus those not receiving the treatment.
  • To explore the relationship between lipid level changes, clinical response, and disease activity markers in belimumab-treated SLE patients.

Main Methods:

  • Retrospective analysis of 41 SLE patients treated with belimumab for at least 6 months.
  • Comparison with a control group of 56 age- and sex-matched SLE patients not on belimumab.
  • Longitudinal assessment of lipid profiles (HDL, LDL, triglycerides, ApoA-I, ApoB) and disease activity markers (IgG, anti-dsDNA, C3, SLEDAI-2K) using Generalized Estimating Equation (GEE) analyses.

Main Results:

  • Belimumab treatment led to a significant sustained increase in high-density lipoprotein (HDL) cholesterol levels over 6 months (7.6% increase from baseline).
  • Significant increases in HDL and apolipoprotein A-I (apoA-I) were observed as early as 1 month into treatment.
  • No significant changes were noted in total cholesterol, triglycerides, LDL cholesterol, or apolipoprotein B. HDL increases were associated with reduced disease activity (IgG, anti-dsDNA, C3) and significant only in patients with a clinical response (≥4-point SLEDAI-2K reduction).

Conclusions:

  • Belimumab treatment can lead to a significant and sustained improvement in HDL cholesterol levels in SLE patients.
  • The observed increase in HDL may be linked to improved control of lupus disease activity.
  • This lipid profile modification could potentially contribute to mitigating cardiovascular risk in SLE patients.