At present, there are very few studies that look at the effect of urem
ia, prednisone and cyclosporine therapy on the lipid profiles of child
ren. This effect is important because of the potential association of
hyperlipidemia and increased risk of cardiovascular morbidity and mort
ality and glomerulosclerosis. We measured fasting lipid profiles in 73
children. There were 21 controls, 18 patients treated with cyclospori
ne and prednisone, 9 patients treated with cyclosporine alone and 25 d
ialysis patients. Lipoprotein (a) levels were measured using direct bi
nding 'sandwich' ELISA. Uremic children had higher levels of triglycer
ides and very-low-density lipoprotein as compared with the control gro
up. Children receiving combination of cyclosporine and prednisone also
had higher total cholesterol, triglycerides, low-density lipoprotein,
very-low-density lipoprotein as compared to the control group. Howeve
r, children receiving cyclosporine monotherapy had lipid profiles simi
lar to the control group. Patients receiving cyclosporine and predniso
ne had higher total cholesterol, high-density lipoprotein and low-dens
ity lipoprotein as compared with the dialysis group. Evaluating lipopr
otein (a) levels, children on cyclosporine monotherapy had lower lipop
rotein (a) levels as compared with children on dialysis and those rece
iving both combination therapy. The total cholesterol/high-density lip
oprotein-cholesterol ratio (TC/HDL) was similar among the study groups
. In summary, uremic children and children receiving steroids with cyc
losporine have elevated lipid levels. However, the increased risk for
atherosclerosis is not evident because of similar levels of lipoprotei
n (a) and TC/HDL ratios among the study groups.