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Updated: Apr 25, 2026

Studies of Chaperone-Cochaperone Interactions using Homogenous Bead-Based Assay
Published on: July 21, 2021
Interaction between thienopyridines and proton pump inhibitors
Banu Sahin Yildiz, Mustafa Yildiz, Ibrahim Akin1
1Department of Cardiology, University of Mannheim, Theodor-Kutzer Ufer, 1-3, 68167 Mannheim, Germany. akinibra@med.uni-rostock.de.
Adenosine diphosphate (ADP) inhibition prevents cardiovascular events. This review examines thienopyridines, P2Y12 inhibitors, and their potential interaction with proton pump inhibitors (PPIs) that may increase cardiac risk.
Area of Science:
- Pharmacology
- Cardiovascular Medicine
- Drug Interactions
Background:
- Adenosine diphosphate (ADP) is critical for thrombus formation, making its inhibition a strategy to prevent cardiovascular events in Acute Coronary Syndrome (ACS) and Percutaneous Coronary Intervention (PCI) patients.
- The P2Y12 receptor, a key target for ADP, is a viable pharmacological target due to its limited tissue distribution.
- Thienopyridines are a class of drugs that irreversibly inhibit the P2Y12 receptor, often used with aspirin.
Purpose of the Study:
- To provide an overview of the pharmacokinetic and pharmacodynamic properties of thienopyridine drugs.
- To critically discuss the suspected interaction between thienopyridines, particularly clopidogrel, and proton pump inhibitors (PPIs).
- To evaluate the impact of this interaction on platelet inhibition and cardiac event risk.
Main Methods:
- Review of existing literature on thienopyridines, P2Y12 inhibition, and PPIs.
- Analysis of pharmacokinetic and pharmacodynamic data for thienopyridine drugs.
- Critical evaluation of studies investigating drug-drug interactions between thienopyridines and PPIs.
Main Results:
- Thienopyridines are effective P2Y12 inhibitors used in cardiovascular disease management.
- A potential interaction exists between thienopyridines (especially clopidogrel) and PPIs.
- This interaction may reduce the antiplatelet effect of thienopyridines, potentially increasing cardiac event risk.
Conclusions:
- Understanding thienopyridine pharmacology is crucial for optimizing ACS and PCI patient care.
- The interaction between thienopyridines and PPIs warrants careful consideration to mitigate risks.
- Further research is needed to fully elucidate and manage this drug interaction.
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