Comparative Study of Effects of Vonoprazan and Esomeprazole on Antiplatelet Function of Clopidogrel or Prasugrel in Relation to CYP2C19 Genotype.

Author: FurutaTakahisa, HamayaYasushi, IwaizumiMoriya, KagamiTakuma, MiyajimaHiroaki, OsawaSatoshi, SugimotoKen, SuzukiTakahiro, UmemuraKazuo, UotaniTakahiro, YamadeMihoko

Paper Details 
Original Abstract of the Article :
Drug-drug interaction between antiacid and antiplatelet agents has not been fully elucidated. Vonoprazan, a new potassium competitive acid blocker, has been available in Japan. CYP2C19 and CYP3A4 are involved in the metabolism of clopidogrel, prasugrel, esomeprazole, and vonoprazan. Using a P2Y12 as...See full text at original site
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引用元:
https://doi.org/10.1002/cpt.863

データ提供:米国国立医学図書館(NLM)

Vonoprazan and Esomeprazole: Impact on Antiplatelet Function

This study explores the complex world of pharmacology, investigating the potential drug-drug interactions between antiacid medications and antiplatelet agents. The researchers are trying to understand how two proton pump inhibitors, vonoprazan and esomeprazole, affect the antiplatelet function of clopidogrel and prasugrel. They conducted a study with 31 healthy volunteers, analyzing the impact of these medications on platelet aggregation based on the CYP2C19 genotype.

Vonoprazan's Greater Impact on Antiplatelet Function

The study found that vonoprazan, a new potassium competitive acid blocker, decreased the antiplatelet function of both clopidogrel and prasugrel more potently than esomeprazole. This suggests that vonoprazan may have a greater impact on platelet function and potentially increase the risk of bleeding when used concurrently with antiplatelet agents.

Dr. Camel's Conclusion

This study highlights the importance of carefully considering potential drug-drug interactions when prescribing medications, particularly for patients taking antiplatelet agents. It underscores the need for ongoing research to better understand the impact of various medications on platelet function and optimize patient safety.
Date :
  1. Date Completed 2019-05-20
  2. Date Revised 2022-12-07
Further Info :

Pubmed ID

28875498

DOI: Digital Object Identifier

10.1002/cpt.863

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English

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