Taql B1/B2 and-629A/C cholesteryl ester transfer protein (CETP) gene polymorphisms and their association with CETP activity and high-density lipoprotein cholesterol levels in a Tehranian population. Part of the Tehran Lipid and Glucose Study ( TLGS)

We examined the cholesteryl ester transfer protein (CETP) gene Taql intron 1 B1/B2 polymorphism and the -629A/C CETP promoter polymorphism in respect to high-density lipoprotein cholesterol (HDL-C) in a healthy Iranian population taken from the Tehran Lipid and Glucose Study (TLGS). The relationship between CETP activity and HDL-C level was also determined along with body mass index, blood pressure and tobacco smoking status. PCR-RFLP used to amplify a segment of the CETP intron 1 Taql (B2/B1) polymorphism from 1021 individuals and we selected 345 individuals from the lowest, middle and highest HDL-C deciles and investigated the -629A/C polymorphism. We also evaluated the CETP activity of 103 of these individuals, each with at least one homozygous allele. The presence of the Taql B2 and -629A/C A alleles were significantly associated with increased HDL-C levels (B2B2 = 1.19 +/- 0.31 mmolL(-1) vs. B1B1 = 1.01 +/- 0.2 mmol L-1 for p < 0.001; AA = 1.15 +/- 0.41 mmol L-1 vs. CC = 0.95 +/- 0.28 mmol L-1 for p < 0.001) and decreased the CETP activity (B1B1 = 67.8 +/- 8.9 pmol L-1 vs. B2B2 = 62.6 +/- 9.6 pmol L-1 for p < 0.01; CC = 68.6 +/- 8.4 pmol L-1 vs. AA = 62.7 +/- 9.7 pmol L-1 for p < 0.002). The frequencies were 0.382 for the Taql B2 allele and 0.462 for the -629A/C A allele, with linkage disequilibrium analysis giving D = 0.0965 and D' = 0.4695. We demonstrated that the Taql B1 and B2 alleles and the -629A/C A and C alleles were in linkage disequilibrium in our population and that there was a significant association between the B2 and A alleles and high HDL-C levels and low CETP activity. Linkage disequilibrium between the Taql A and B2 alleles also detected.