Low-dose aspirin, coxibs, and other NSAIDS: a clinical mosaic emerges.

Aspirin has been a commercial drug for over a century, although for most of this history, an understanding of its mechanism of action, as an inhibitor of cyclooxygenase (COX) activity and thus of prostanoid synthesis, was lacking. Over the past fifty years, a large number of other nonsteroidal antii...

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Bibliografische gegevens
Hoofdauteurs: Patrono, C, Baigent, C
Formaat: Journal article
Taal:English
Gepubliceerd in: 2009
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author Patrono, C
Baigent, C
author_facet Patrono, C
Baigent, C
author_sort Patrono, C
collection OXFORD
description Aspirin has been a commercial drug for over a century, although for most of this history, an understanding of its mechanism of action, as an inhibitor of cyclooxygenase (COX) activity and thus of prostanoid synthesis, was lacking. Over the past fifty years, a large number of other nonsteroidal antiinflammatory drugs (NSAIDs) have been developed, and a much deeper understanding of inflammation and prostanoid action has emerged. Indeed, a new class of selective inhibitors of the cyclooxygenase-2 isozyme was introduced, about ten years ago, and these so-called coxibs quickly became regarded as preferable, in certain clinical contexts, to avoid side effects associated with the use of aspirin and previously developed NSAIDs. This regard for coxibs has been challenged, sometimes infamously, as cardiovascular events associated with coxib use have become apparent. A variety of clinical trials have led to seemingly conflicting data concerning the roles of COX-1 and COX-2, and the implications of their relative inhibition, in cardiovascular health and disease. In this Review, the authors offer an assessment of drug pharmacokinetics and enzyme physiology that reconciles cardiovascular appraisals from a wide array of clinical data.
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spelling oxford-uuid:fa04c388-b1a9-4e0e-98c7-f4524e54af142022-03-27T13:02:25ZLow-dose aspirin, coxibs, and other NSAIDS: a clinical mosaic emerges.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:fa04c388-b1a9-4e0e-98c7-f4524e54af14EnglishSymplectic Elements at Oxford2009Patrono, CBaigent, CAspirin has been a commercial drug for over a century, although for most of this history, an understanding of its mechanism of action, as an inhibitor of cyclooxygenase (COX) activity and thus of prostanoid synthesis, was lacking. Over the past fifty years, a large number of other nonsteroidal antiinflammatory drugs (NSAIDs) have been developed, and a much deeper understanding of inflammation and prostanoid action has emerged. Indeed, a new class of selective inhibitors of the cyclooxygenase-2 isozyme was introduced, about ten years ago, and these so-called coxibs quickly became regarded as preferable, in certain clinical contexts, to avoid side effects associated with the use of aspirin and previously developed NSAIDs. This regard for coxibs has been challenged, sometimes infamously, as cardiovascular events associated with coxib use have become apparent. A variety of clinical trials have led to seemingly conflicting data concerning the roles of COX-1 and COX-2, and the implications of their relative inhibition, in cardiovascular health and disease. In this Review, the authors offer an assessment of drug pharmacokinetics and enzyme physiology that reconciles cardiovascular appraisals from a wide array of clinical data.
spellingShingle Patrono, C
Baigent, C
Low-dose aspirin, coxibs, and other NSAIDS: a clinical mosaic emerges.
title Low-dose aspirin, coxibs, and other NSAIDS: a clinical mosaic emerges.
title_full Low-dose aspirin, coxibs, and other NSAIDS: a clinical mosaic emerges.
title_fullStr Low-dose aspirin, coxibs, and other NSAIDS: a clinical mosaic emerges.
title_full_unstemmed Low-dose aspirin, coxibs, and other NSAIDS: a clinical mosaic emerges.
title_short Low-dose aspirin, coxibs, and other NSAIDS: a clinical mosaic emerges.
title_sort low dose aspirin coxibs and other nsaids a clinical mosaic emerges
work_keys_str_mv AT patronoc lowdoseaspirincoxibsandothernsaidsaclinicalmosaicemerges
AT baigentc lowdoseaspirincoxibsandothernsaidsaclinicalmosaicemerges