TY - JOUR
T1 - Variants in the APOA5 gene region and the response to combination therapy with statins and fenofibric acid in a randomized clinical trial of individuals with mixed dyslipidemia
AU - Brautbar, Ariel
AU - Covarrubias, Daniel
AU - Belmont, John
AU - Lara-Garduno, Fremiet
AU - Virani, Salim S.
AU - Jones, Peter H.
AU - Leal, Suzanne M.
AU - Ballantyne, Christie M.
N1 - Funding Information:
DNA extraction and genotyping funded by Abbott Pharmaceuticals.
PY - 2011/12
Y1 - 2011/12
N2 - Objective: Atherogenic dyslipidemia is highly associated with coronary heart disease and is characterized by elevated triglycerides (TG), low high-density lipoprotein cholesterol (HDL-C), and elevated low-density lipoprotein cholesterol (LDL-C). The combination of statins and fibrates is a common modality to treat individuals with atherogenic dyslipidemia. We sought to identify single nucleotide polymorphisms (SNPs) associated with HDL-C, TG, and apolipoprotein A1 (ApoA-I) response to combination therapy with statins and fenofibric acid (FA) in individuals with atherogenic dyslipidemia. Methods: 2228 individuals with mixed dyslipidemia who were participating in a multicenter, randomized, double-blind, active-controlled study comparing FA alone, in combination with a statin, or statin alone for a 12-week period, were genotyped for 304 candidate SNPs. A multivariate linear regression analysis for percent change in HDL-C, ApoA-I and TG levels was performed. Results: SNPs in the apolipoprotein (APO) A5-ZNF259 region rs3741298 (P=1.8×10 -7), rs964184 (P=3.6×10 -6), rs651821 (P=4.5×10 -5), and rs10750097 (P=1×10 -4), were significantly associated with HDL-C response to combination therapy with statins and FA, with a similar association identified for ApoA-I. A haplotype composed of the minor alleles of SNPs rs3741298, rs964184, and rs10750097, was associated with a positive response to statins and FA (P=8.7×10 -7) and had a frequency of 18% in the study population. Conclusion: In a population with atherogenic dyslipidemia, common SNPs and haplotypes within the APOA5-ZNF259 region are highly associated with HDL-C and ApoA-I response to combination therapy with statins and FA.
AB - Objective: Atherogenic dyslipidemia is highly associated with coronary heart disease and is characterized by elevated triglycerides (TG), low high-density lipoprotein cholesterol (HDL-C), and elevated low-density lipoprotein cholesterol (LDL-C). The combination of statins and fibrates is a common modality to treat individuals with atherogenic dyslipidemia. We sought to identify single nucleotide polymorphisms (SNPs) associated with HDL-C, TG, and apolipoprotein A1 (ApoA-I) response to combination therapy with statins and fenofibric acid (FA) in individuals with atherogenic dyslipidemia. Methods: 2228 individuals with mixed dyslipidemia who were participating in a multicenter, randomized, double-blind, active-controlled study comparing FA alone, in combination with a statin, or statin alone for a 12-week period, were genotyped for 304 candidate SNPs. A multivariate linear regression analysis for percent change in HDL-C, ApoA-I and TG levels was performed. Results: SNPs in the apolipoprotein (APO) A5-ZNF259 region rs3741298 (P=1.8×10 -7), rs964184 (P=3.6×10 -6), rs651821 (P=4.5×10 -5), and rs10750097 (P=1×10 -4), were significantly associated with HDL-C response to combination therapy with statins and FA, with a similar association identified for ApoA-I. A haplotype composed of the minor alleles of SNPs rs3741298, rs964184, and rs10750097, was associated with a positive response to statins and FA (P=8.7×10 -7) and had a frequency of 18% in the study population. Conclusion: In a population with atherogenic dyslipidemia, common SNPs and haplotypes within the APOA5-ZNF259 region are highly associated with HDL-C and ApoA-I response to combination therapy with statins and FA.
KW - Combination therapy
KW - Genetic variants
KW - Mixed dyslipidemia
UR - http://www.scopus.com/inward/record.url?scp=82955247614&partnerID=8YFLogxK
U2 - 10.1016/j.atherosclerosis.2011.08.015
DO - 10.1016/j.atherosclerosis.2011.08.015
M3 - Article
C2 - 21889769
AN - SCOPUS:82955247614
SN - 0021-9150
VL - 219
SP - 737
EP - 742
JO - Atherosclerosis
JF - Atherosclerosis
IS - 2
ER -