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[Recent development of selective cyclooxygenase-2 inhibitors].

Abstract
Nonsteroidal anti-inflammatory drugs(NSAIDs) are clinically effective against the inflammatory symptoms of rheumatoid arthritis. Recent attention has been focused on selective cyclooxygenase(COX)-2 inhibitors, a type of NSAID that inhibits a subtype of COX. Because of the different actions of COX-1 and COX-2, selective COX-2 inhibitors were expected to reduce adverse reactions such as gastrointestinal disorders. Various clinical studies have confirmed that the efficacy of COX-2 inhibitors for RA is similar to that of conventional NSAIDs, but they cause fewer severe gastrointestinal disorders. The incidence of complications related to renal dysfunction, such as edema and hypertension, is not different. Patients using selective COX-2 inhibitors have recently been reported to show an increase in thrombotic complications such as myocardial infarction. Therefore, more data on adverse events should be collected in the future from large-scale clinical studies to further clarify the actual value of selective COX-2 inhibitors.
AuthorsShinichi Kawai
JournalNihon rinsho. Japanese journal of clinical medicine (Nihon Rinsho) Vol. 60 Issue 12 Pg. 2370-7 (Dec 2002) ISSN: 0047-1852 [Print] Japan
PMID12510364 (Publication Type: English Abstract, Journal Article, Review)
Chemical References
  • Anti-Inflammatory Agents, Non-Steroidal
  • Cyclooxygenase 2 Inhibitors
  • Cyclooxygenase Inhibitors
  • Isoenzymes
  • Membrane Proteins
  • Prostaglandins
  • Cyclooxygenase 1
  • Cyclooxygenase 2
  • PTGS1 protein, human
  • PTGS2 protein, human
  • Prostaglandin-Endoperoxide Synthases
  • Ptgs1 protein, rat
Topics
  • Animals
  • Anti-Inflammatory Agents, Non-Steroidal
  • Arthritis, Rheumatoid (drug therapy)
  • Cyclooxygenase 1
  • Cyclooxygenase 2
  • Cyclooxygenase 2 Inhibitors
  • Cyclooxygenase Inhibitors (adverse effects, therapeutic use)
  • Digestive System (drug effects)
  • Humans
  • Isoenzymes (antagonists & inhibitors, chemistry)
  • Kidney Diseases (chemically induced)
  • Membrane Proteins
  • Myocardial Infarction (chemically induced)
  • Prostaglandin-Endoperoxide Synthases (chemistry)
  • Prostaglandins (metabolism)
  • Rats

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