Selective COX-2 Inhibition Improves Endothelial Function in Coronary Artery Disease
| Autor: | Rémy Chenevard, David Hürlimann, Markus Béchir, Frank Enseleit, Lukas Spieker, Matthias Hermann, Walter Riesen, Steffen Gay, Renate E. Gay, Michel Neidhart, Beat Michel, Thomas F. Lüscher, Georg Noll, Frank Ruschitzka |
|---|---|
| Rok vydání: | 2003 |
| Předmět: |
Male
medicine.medical_specialty Endothelium Coronary Artery Disease Placebo Coronary artery disease Double-Blind Method Physiology (medical) Internal medicine medicine.artery medicine Humans Cyclooxygenase Inhibitors Brachial artery Aged Ultrasonography Sulfonamides Aspirin Cross-Over Studies Cyclooxygenase 2 Inhibitors Vascular disease business.industry Membrane Proteins Arteriosclerosis Middle Aged medicine.disease Isoenzymes Lipoproteins LDL Vasodilation C-Reactive Protein medicine.anatomical_structure Celecoxib Cyclooxygenase 2 Prostaglandin-Endoperoxide Synthases Anesthesia Cardiology Pyrazoles Endothelium Vascular Cardiology and Cardiovascular Medicine business Biomarkers medicine.drug |
| Zdroj: | Circulation. 107:405-409 |
| ISSN: | 1524-4539 0009-7322 |
| DOI: | 10.1161/01.cir.0000051361.69808.3a |
| Popis: | Background— There is an ongoing debate as to whether the gastrointestinal safety of COX-2 inhibition compared with nonsteroidal antiinflammatory drugs (NSAIDs) may come at the cost of increased cardiovascular events. In view of the large number of patients at cardiovascular risk requiring chronic analgesic therapy with COX-2 inhibitors for arthritic and other inflammatory conditions, the effects of selective COX-2 inhibition on clinically useful surrogates for cardiovascular disease, particularly endothelial function, need to be determined. Methods and Results— Fourteen male patients (mean age, 66±3 years) with severe coronary artery disease (average of 2.6 vessels with stenosis >75%) undergoing stable background therapy with aspirin and statins were included. The patients received celecoxib (200 mg BID) or placebo for a duration of 2 weeks in a double-blind, placebo-controlled, crossover fashion. After each treatment period, flow-mediated dilation of the brachial artery, high-sensitivity C-reactive protein, oxidized LDL, and prostaglandins were measured. Celecoxib significantly improved endothelium-dependent vasodilation compared with placebo (3.3±0.4% versus 2.0±0.5%, P =0.026), whereas endothelium-independent vasodilation, as assessed by nitroglycerin, remained unchanged (9.0±1.6% versus 9.5±1.3%, P =0.75). High-sensitivity C-reactive protein was significantly lower after celecoxib (1.3±0.4 mg/L) than after placebo (1.8±0.5 mg/L, P =0.019), as was oxidized LDL (43.6±2.4 versus 47.6±2.6 U/L, P =0.028), whereas prostaglandins did not change. Conclusions— This is the first study to demonstrate that selective COX-2 inhibition improves endothelium-dependent vasodilation and reduces low-grade chronic inflammation and oxidative stress in coronary artery disease. Thus, selective COX-2 inhibition holds the potential to beneficially impact outcome in patients with cardiovascular disease. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
|