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Pharmacogenomics in cardiovascular disease: focus on aspirin and ADP receptor antagonists
被引:25
作者:
Wurtz, M.
[1
]
Lordkipanidze, M.
[2
]
Grove, E. L.
[1
]
机构:
[1] Aarhus Univ Hosp, Dept Cardiol, DK-8200 Aarhus, Denmark
[2] Univ Birmingham, Ctr Cardiovasc Sci, Inst Biomed Res, Coll Med & Dent Sci, Birmingham, W Midlands, England
关键词:
ADP receptor antagonists;
aspirin;
cardiovascular disease;
clopidogrel;
pharmacogenomics;
PERCUTANEOUS CORONARY INTERVENTION;
CLOPIDOGREL PLATELET REACTIVITY;
CYTOCHROME-P450;
2C19;
GENOTYPE;
OF-FUNCTION POLYMORPHISM;
PROTON PUMP INHIBITORS;
807 C/T POLYMORPHISM;
CYP2C19;
GENETIC POLYMORPHISMS;
STENT THROMBOSIS;
RESPONSE VARIABILITY;
D O I:
10.1111/jth.12318
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Antiplatelet agents like aspirin and adenosine diphosphate receptor antagonists are effective in reducing recurrent ischemic events. Considerable inter-individual variability in the platelet inhibition obtained with these drugs has initiated a search for explanatory mechanisms and ways to improve treatment. In recent years, numerous genetic polymorphisms have been linked with reduced platelet inhibition and lack of clinical efficacy of antiplatelet drugs, particularly clopidogrel and aspirin. Consequently, attempts to adjust antiplatelet treatment according to genotype have been made, but the clinical benefit has been modest in studies performed so far. The progress in genome science over the last decade and the declining cost of sequencing technologies hold the promise of enabling genetically tailored antiplatelet therapy. However, more evidence is needed to clarify which polymorphisms may serve as targets to improve treatment. The present review outlines the panel of polymorphisms affecting the benefit of aspirin and adenosine diphosphate receptor antagonists, including novel and ongoing studies evaluating whether genotyping may be beneficial in tailoring antiplatelet therapy.
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页码:1627 / 1639
页数:13
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