Background-The gene encoding the target of calcium channel blockers, the (alpha)1c-subunit of the L-type calcium channel (CACNA1C), has not been well characterized, and only small pharmacogenetic studies testing this gene have been published to date. Methods and Results-Resequencing of CACNA1C was performed followed by a nested case-control study of the INternational VErapamil SR/trandolapril STudy (INVEST) GENEtic Substudy (INVEST-GENES). Of 46 polymorphisms identified, 8 were assessed in the INVEST-GENES. Rs1051375 was found to have a significant interaction with treatment strategy (P=0.0001). Rs1051375 A/A genotype was associated with a 46% reduction in the primary outcome among those randomized to verapamil SR treatment, when compared with atenolol treatment (odds ratio 0.54 95% CI 0.32 to 0.92). In heterozygous A/G individuals, there was no difference in the occurrence of the primary outcome when randomized to verapamil SR versus atenolol treatment (odds ratio 1.47 95% CI 0.86 to 2.53), whereas homozygous G/G individuals had a greater than 4-fold increased risk of the primary outcome with verapamil treatment compared with those randomized to atenolol treatment (odds ratio 4.59 95% CI 1.67 to 12.67). We did not identify allelic expression imbalance or differences in mRNA expression in heart tissue by rs1051375 genotype. Conclusions-Variation in CACNA1C is associated with treatment response among hypertensive patients with stable coronary artery disease. Our data suggest a genetically defined group of patients that benefit most from calcium channel blocker therapy, a group that benefits most from =-blocker therapy, and a third group in which calcium channel blocker and (beta)-blocker therapy are equivalent. Copyright (copyright) 2009 American Heart Association. (copyright) 2009 American Heart Association, Inc.
CITATION STYLE
A.L., B., H., N., D., W., Y., G., J., W., J.I., M., … J.A., J. (2009). CACNA1C gene polymorphisms, cardiovascular disease outcomes, and treatment response. Circulation: Cardiovascular Genetics, 2(4), 362–370. Retrieved from http://www.embase.com/search/results?subaction=viewrecord&from=export&id=L358874445
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