Abstract

BackgroundThe present study was conducted to investigate the possible outcome of interaction between endothelial nitric oxide (NOS3) G894T and cholesteryl ester transfer TaqIB variants on the risk of coronary artery disease (CAD) and type 2 diabetes mellitus (T2DM). The sample included a total of 207 CAD patients (102 CAD patients with T2DM and 105 CAD patients without T2DM). There were also 101 patients with T2DM and 92 age- and sex-matched healthy individuals as controls. All study participants were from Western Iran. The sample was genotyped by polymerase chain reaction-restriction fragment length polymorphism.ResultsThe presence of NOS3 T allele was not associated with the risk of CAD or T2DM, and the CETP B1 allele was only significantly associated with the increased risk of CAD in total CAD patients (odds ratio (OR) = 5.1, p = 0.019). However, the concomitant presence of both CETP B1 and NOS3 T alleles significantly increased the risk of CAD in total CAD patients (OR = 18.1, p < 0.001), in CAD patients without T2DM (OR = 27.1, p = 0.03), and in CAD patients with T2DM (OR = 13.5, p = 0.002). Also, the presence of both alleles increased the risk of T2DM (OR = 12, p = 0.004).ConclusionsOur findings, for the first time, indicate that NOS3 T allele strongly interacts with CETP B1 allele to augment the risk of CAD and T2DM in the population of Western Iran.

Highlights

  • Cholesteryl ester transfer protein (CETP) participates in reverse cholesterol transport by transfering cholesteryl esters from high-density lipoprotein-cholesterol (HDLC) to apolipoprotein-B containing particles in exchange for triglycerides (TG), thereby reducing the concentration of HDL-C [1,2,3].CETP gene located on chromosome 16q21 consists of 16 exons and 15 introns and has several genetic polymorphisms affecting CETP activity among which TaqIB polymorphism has been most widely studied

  • The plasma level of low-density lipoprotein-cholesterol (LDL-C) and TG was significantly higher, and HDL-C level was significantly lower in both coronary artery disease (CAD) and type 2 diabetes mellitus (T2DM) patients compared to controls

  • Higher level of TG and lower level of HDL-C were observed in CAD/T2DM patients

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Summary

Introduction

CETP gene located on chromosome 16q21 consists of 16 exons and 15 introns and has several genetic polymorphisms affecting CETP activity among which TaqIB polymorphism has been most widely studied This polymorphism results from G to A base pair change at nucleotide 277 in intron 1 of the CETP gene which disrupts TaqI restriction site (single-nucleotide polymorphism (SNP) rs708272). The association of CETP variants with coronary artery disease (CAD) and type 2 diabetes mellitus (T2DM) has been investigated in several studies without consistent results [1,6,7,8,9]. The present study was conducted to investigate the possible outcome of interaction between endothelial nitric oxide (NOS3) G894T and cholesteryl ester transfer TaqIB variants on the risk of coronary artery disease (CAD) and type 2 diabetes mellitus (T2DM). The sample was genotyped by polymerase chain reaction-restriction fragment length polymorphism

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