COX-2 inhibitors and cardiovascular risk. Inferences based on biology and clinical studies

Thromb Haemost. 2006 Oct;96(4):401-6.

Abstract

Even though non-steroidal anti-inflammatory drugs (NSAIDs) have been widely used for a long time, the search continues for anti-inflammatory drugs with few side-effects. COX-2 inhibitors are currently most debated, because they have less gastrointestinal side effects but have been linked to increased cardiovascular morbidity and mortality, presumably related to thrombotic events. This has brought about the withdrawal of rofecoxib and other COX-2 inhibitors from the market. Although the results of several large studies with prospective, randomized design and meta-analysis of different trials have led to the demise of many popular COX-2 inhibitors, yet the conclusion seems to be rather simplistic. This review presents evidence from basic biology and clinical studies with the expectation that a balanced position, particularly in relation to increase in cardiovascular events, may be elucidated.

Publication types

  • Review

MeSH terms

  • Animals
  • Blood Platelets / drug effects*
  • Blood Platelets / metabolism
  • Cardiovascular Diseases / chemically induced*
  • Cardiovascular Diseases / metabolism
  • Celecoxib
  • Cyclooxygenase 2 / metabolism
  • Cyclooxygenase 2 Inhibitors / adverse effects*
  • Diclofenac / adverse effects
  • Diclofenac / analogs & derivatives
  • Drug Labeling
  • Endothelium, Vascular / drug effects*
  • Endothelium, Vascular / metabolism
  • Epoprostenol / metabolism
  • Humans
  • Lactones / adverse effects
  • Platelet Aggregation
  • Product Surveillance, Postmarketing
  • Pyrazoles / adverse effects
  • Randomized Controlled Trials as Topic
  • Risk Assessment
  • Sulfonamides / adverse effects
  • Sulfones / adverse effects
  • Thromboxane A2 / metabolism

Substances

  • Cyclooxygenase 2 Inhibitors
  • Lactones
  • Pyrazoles
  • Sulfonamides
  • Sulfones
  • rofecoxib
  • Diclofenac
  • Thromboxane A2
  • Epoprostenol
  • Cyclooxygenase 2
  • Celecoxib
  • lumiracoxib