Low dose rofecoxib, inflammation and prostacyclin synthesis in acute coronary syndromes

Rocz Akad Med Bialymst. 2005:50:339-42.

Abstract

Purpose: To assess the influence of low dose rofecoxib on inflammatory mediators and prostacyclin synthesis in patients with acute coronary syndromes (ACS) in a short-term follow up.

Material and methods: Twenty nine patients with ACS without ST elevation were randomized to simvastatin alone or together with low dose rofecoxib. Serum levels of interleukin 6 (IL-6), 6-keto-PGF-1alpha--stable product of prostacyclin (PGT2) and hs-C-reactive protein (hs-CRP) were assessed on enrollment and after 30-day follow up.

Results: Combination of rofecoxib with statin significantly decreased levels of hs-CRP after one month therapy (5.21 mg/l +/- 4.12 vs 2.11 mg/l +/- 2.1; p=0.0092). This effect was not evident in a group on statin alone (3.95 mg/l +/- 3.33 vs 2.48 mg/l +/- 2.39; p=0.31). 6-keto-PGF-1alpha increased not significantly in both groups. IL-6 concentration has not changed during follow up.

Conclusions: Low dose of selective COX-2 inhibitor exerts significant anti-inflammatory effect and does not diminish PG12 synthesis in study group of patients with ACS.

Publication types

  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • 6-Ketoprostaglandin F1 alpha / blood
  • Acute Disease
  • Aged
  • Anti-Inflammatory Agents, Non-Steroidal / administration & dosage*
  • Anticholesteremic Agents / administration & dosage
  • C-Reactive Protein / metabolism
  • Coronary Disease / blood
  • Coronary Disease / drug therapy*
  • Dose-Response Relationship, Drug
  • Drug Therapy, Combination
  • Epoprostenol / biosynthesis*
  • Female
  • Follow-Up Studies
  • Humans
  • Inflammation Mediators / metabolism*
  • Interleukin-6 / blood
  • Lactones / administration & dosage*
  • Male
  • Middle Aged
  • Simvastatin / administration & dosage
  • Sulfones / administration & dosage*
  • Syndrome

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Anticholesteremic Agents
  • Inflammation Mediators
  • Interleukin-6
  • Lactones
  • Sulfones
  • rofecoxib
  • 6-Ketoprostaglandin F1 alpha
  • C-Reactive Protein
  • Simvastatin
  • Epoprostenol