Publication Date

6-1-2022

Journal

Cardiovascular Drugs and Therapy

DOI

10.1007/s10557-021-07224-9

PMID

34245446

PMCID

PMC8271326

PubMedCentral® Posted Date

7-10-2021

PubMedCentral® Full Text Version

Post-Print

Published Open-Access

yes

Keywords

Adenosine, Animals, Aspirin, Dipyridamole, Hydroxymethylglutaryl-CoA Reductase Inhibitors, Rats, Vasodilator Agents, Dipyridamole, Coronary artery disease, Adenosine, Statins, Infarct size, Platelets, Phosphodiesterase inhibitors

Abstract

Dipyridamole is an old anti-platelet and coronary vasodilator agent that inhibits platelet phosphodiesterase and increases interstitial adenosine levels. Its use in coronary artery disease (CAD) has fallen out of practice in the modern era with the advent of new anti-platelet agents, and most modern guidelines on the management of CAD either neglect to comment on its utility or outright recommend against it. The majority of the studies used in these guidelines are outdated and took place in an era when high doses of aspirin were used and statins were not widely utilized. There is growing evidence in rat models of dipyridamole's synergy with statins through adenosine modulation resulting in significant myocardial protection against ischemia-reperfusion injury and limitation of infract size. The data in human studies are limited but show a similar potential synergy between dipyridamole and statins. It would thus be prudent to reconsider the recommendations against the use of dipyridamole in CAD and to re-evaluate its possible role and potential benefits through well-designed randomized trials combining it with statins, low-dose aspirin, and/or other anti-platelet agents.

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