APOE Polymorphisms Contribute to Reduced Atorvastatin Response in Chilean Amerindian Subjects
AbstractGenetic factors can determine the high variability observed in response to lipid-lowering therapy with statins. Nonetheless, the frequency of single nucleotide polymorphisms (SNPs) and their impact can vary due to ethnicity. Because the Chilean population carries a strong Amerindian background, the objective of this study was to evaluate the influence of apolipoprotein E (APOE) variants (rs429358, rs7412) and the 1959C>T SNP (rs5925) in the low-density lipoprotein receptor (LDLR) in response to atorvastatin treatment in hypercholesterolemic individuals. A hundred and thirty nine subjects undergoing statin therapy were included. Identification of Amerindian mtDNA haplogroups was determined by polymerase chain reaction (PCR) and PCR followed by restriction fragment length polymorphism (RFLP), respectively. SNPs were determined by PCR-RFLP. Out of the 139 individuals studied, 84.4% had an Amerindian background, according to mtDNA analysis. In relation to APOE variants, carriers of the E3/4 genotype presented lower cholesterol reduction compared to genotype E3/3 (LDL-C: −18% vs. −29%, p ˂ 0.001). On the other hand, the LDLR rs5925 SNP was not related to atorvastatin response (p = 0.5760). Our results suggest that APOE SNPs are potential predictors to atorvastatin therapy in Amerindian Chilean subjects. View Full-Text
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Lagos, J.; Zambrano, T.; Rosales, A.; Salazar, L.A. APOE Polymorphisms Contribute to Reduced Atorvastatin Response in Chilean Amerindian Subjects. Int. J. Mol. Sci. 2015, 16, 7890-7899.
Lagos J, Zambrano T, Rosales A, Salazar LA. APOE Polymorphisms Contribute to Reduced Atorvastatin Response in Chilean Amerindian Subjects. International Journal of Molecular Sciences. 2015; 16(4):7890-7899.Chicago/Turabian Style
Lagos, Jenny; Zambrano, Tomás; Rosales, Alexy; Salazar, Luis A. 2015. "APOE Polymorphisms Contribute to Reduced Atorvastatin Response in Chilean Amerindian Subjects." Int. J. Mol. Sci. 16, no. 4: 7890-7899.