To contribute to the analysis of the genetic background of atheroscler
osis, especially endothelial dysfunction, we searched for DNA polymorp
hisms in the genes encoding E-, P-, and L-selectin, and ICAM-I and VCA
M-I. We detected 17 mutations by single-strand conformation polymorphi
sms analysis and direct sequencing. Five of them resulted in an amino
acid substitution. In E-selectin, exchanges from serine to arginine (p
osition 128), from leucine to phenylalanine (position 554), and a DNA
mutation from guanine to thymine (position 98) present significantly d
ifferent allele frequencies in young patients with angiographically es
tablished, severe atherosclerosis, compared with an unselected populat
ion. Results suggest that these polymorphisms are associated with a hi
gher risk for early severe atherosclerosis.