The association of genetic markers at the apolipoprotein B gene (APOB) (Xbal, Mspl, and ZscoRI polymorphisms) and the lipoprotein lipase gene (LPL) (PvuU polymorphism) with coronary artery disease (CAD) and with variation in plasma lipid levels (total cholesterol, high-density lipoprotein cholesterol, and total triglycerides) was studied in 94 male patients with CAD diagnosed by angiography and in 122 unrelated men of Russian descent free of clinical signs of CAD. The frequent allele (M + ) of the APOB Mspl RFLP was seen more frequently in CAD patients than in control subjects (0.963 vs. 0.898, p < 0.025). No significant differences in allele frequencies were observed for the APOB Xbal and EcoRl polymorphisms or for the LPL Pvull polymorphism. In patients, carriers of the rare allele ( E - ) of the EcoRl RFLP had higher mean triglyceride levels than homozygotes for E+ (p < 0.05). No significant differences in lipid variables were determined for the other three polymorphisms studied. Analysis of intragenotype variances and the multivariate measure of mean values of lipid concentrations showed that genetic variability within the APOB locus may contribute to a certain extent to the level and variability of serum lipid levels in this Russian population.
Stepanov, Vadim A.; Puzyrev, Valery P.; Karpov, Rostislav S.; and Kutmin, Alexey I.
"Genetic Markers in Coronary Artery Disease in a Russian Population,"
1, Article 4.
Available at: https://digitalcommons.wayne.edu/humbiol/vol70/iss1/4