Objectives
Systemic lupus erythematosus (SLE) associates with accelerated atherosclerotic cardiovascular disease. SLE patients have adverse lipoprotein parameters, but little is known about how these change with treatment and disease activity. The NMR LipoProfile test® contains a glycoprotein signal termed GlycA, an inflammatory marker, which has not been evaluated in SLE. We assessed patients longitudinally to determine how lipoproteins and GlycA change with active SLE.
Methods
Sera from selected clinical visits of patients in the Hopkins Lupus Cohort were analyzed for lipoprotein and GlycA levels. Univariate and multivariate analyses were performed to evaluate lipoprotein parameters and their relationship to ethnicity, disease activity, prednisone use and hydroxychloroquine therapy.
Results
52 patients were included over 229 visits. Adverse changes in lipoprotein parameters with disease activity were demonstrated. For each point increase in SLEDAI there was a decrease in high-density lipoprotein (HDL) even after adjusting for corticosteroid use. Prednisone associated with higher VLDL, LDL, HDL and triglycerides. Hydroxychloroquine associated with more favorable parameters. GlycA levels were higher than in normal populations and increased with disease activity.
Conclusion
Adverse changes in lipoprotein profiles associated with SLE activity and prednisone therapy. This gives insight into mechanisms of atherosclerosis in SLE. Favorable lipoprotein parameters occurred in those taking hydroxychloroquine. GlycA increased with disease activity and was higher than in healthy populations.