Effect of Genetic Variant (rs11887534) inABCG8Gene in Coronary Artery Disease and Response to Atorvastatin Therapy

Abstract

Background:ATP-binding cassette transporter ABCG8 plays an important role in excretion of cholesterol from liver. Common genetic polymorphisms inABCG8gene may genetically predispose an individual to coronary artery disease (CAD) along with response to atorvastatin therapy. Thus, we aimed to examine the role ofABCG8D19H polymorphism (rs11887534) in susceptibility to CAD and its influence on atorvastatin response.Methodology:The study included 213 CAD patients and 220 controls. Genotyping ofABCG8D19H polymorphism was done by PCR-RFLP.Results:Our results showed that ABCG8 ‘H’ allele was conferring significant risk for CAD in a dominant model (OR = 2.54;p= 0.014). This increased risk for CAD was more pronounced in males (OR = 2.69;p= 0.030). No correlation ofABCG8genotypes with the risk factors (diabetes, hypertension and smoking) of CAD was observed. On atorvastatin treatment there was a significant decrease in the LDL-C levels (p= 0.021). However, stepwise multiple regression analysis showed that this decease was not associated withABCG8genetic variant (p= 0.845). Observed determinants of variation in interindividual response to atorvastatin therapy were pre-treatment LDL-C (p= 0.024) and TC (p= 0.017).Conclusion:Although the genetic variant 19H ofABCG8confers risk for CAD in North Indian population, it is not associated with interindividual response to atorvastatin therapy.