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Clin Transl Sci ; 10(2): 102-109, 2017 03.
Article in English | MEDLINE | ID: mdl-28075528

ABSTRACT

Genetic variation in the platelet endothelial aggregation receptor 1 (PEAR1) gene, most notably rs12041331, is implicated in altered on-aspirin platelet aggregation and increased cardiovascular event risk. We prospectively tested the effects of aspirin administration at commonly prescribed doses (81, 162, and 324 mg/day) on agonist-induced platelet aggregation by rs12041331 genotype in 67 healthy individuals. Prior to aspirin administration, rs12041331 minor allele carriers had significantly reduced adenosine diphosphate (ADP)-induced platelet aggregation compared with noncarriers (P = 0.03) but was not associated with other platelet pathways. In contrast, rs12041331 was significantly associated with on-aspirin platelet aggregation when collagen and epinephrine were used to stimulate platelet aggregation (P < 0.05 for all associations), but not ADP. The influence of PEAR1 rs12041331 on platelet aggregation is pathway-specific and is altered by aspirin at therapeutic doses, but not in a dose-dependent manner. Additional studies are needed to determine the impact of PEAR1 on cardiovascular events in aspirin-treated patients.


Subject(s)
Aspirin/pharmacology , Platelet Aggregation Inhibitors/pharmacology , Platelet Aggregation/drug effects , Polymorphism, Single Nucleotide , Receptors, Cell Surface/genetics , Adenosine Diphosphate/pharmacology , Adult , Alleles , Amish/genetics , Biomarkers/urine , Blood Platelets/drug effects , Blood Platelets/metabolism , Collagen/pharmacology , Epinephrine/pharmacology , Female , Genotype , Healthy Volunteers , Humans , Male , Middle Aged , Prospective Studies , Thromboxane B2/urine
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