Hypercholesterolemia has been related to aortic valve stenosis (AS). Polymo
rphisms of apolipoproteins (apo) AI, B, and E are associated with variable
levels of plasma lipids, but the association between these polymorphisms an
d AS is unknown. In a case-control study of groups matched by age, sex, com
parable body mass index, hypertension, triglycerides, high-density lipoprot
ein (HDL) cholesterol, and low-density lipoprotein (LDL) cholesterol, we an
alyzed the distribution of apo AI A/G mutation, apo B signal peptide insert
ion/deletion, apo B XbaI restriction fragment length, and apo E polymorphis
ms in 62 non-diabetic patients with severe aortic valve stenosis and 62 con
trol subjects. All patients underwent echocardiographic analysis. Univariat
e analysis showed a higher prevalence of the XbaI X + /X + genotype (p = 0.
007) of apo B and the apo E2 allele (p = 0.034) in patients with severe AS.
Apo polymorphisms were not associated with lipid levels, left ventricular
mass, or the aortic gradient.