Cargando…
Cox-2: where are we in 2003? - Cardiovascular risk and Cox-2 inhibitors
Selective cyclooxygenase-2 (COX-2) inhibitors were developed to reduce the gastrointestinal toxicity of conventional nonsteroidal anti-inflammatory agents. However, COX-2 inhibitors decrease prostacyclin production and may disrupt the normal homeostatic balance, leading to a prothrombotic state and...
Autores principales: | , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2003
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC154429/ https://www.ncbi.nlm.nih.gov/pubmed/12716442 http://dx.doi.org/10.1186/ar609 |
_version_ | 1782120748915097600 |
---|---|
author | Mukherjee, Debabrata Topol, Eric J |
author_facet | Mukherjee, Debabrata Topol, Eric J |
author_sort | Mukherjee, Debabrata |
collection | PubMed |
description | Selective cyclooxygenase-2 (COX-2) inhibitors were developed to reduce the gastrointestinal toxicity of conventional nonsteroidal anti-inflammatory agents. However, COX-2 inhibitors decrease prostacyclin production and may disrupt the normal homeostatic balance, leading to a prothrombotic state and offsetting the potential gastrointestinal benefits. Available clinical data and basic biological studies raise significant concern about the potential prothrombotic effect of this class of drugs. Two recent studies with a newer, more selective COX-2 inhibitor have added to the already existing concern about the cardiovascular safety of these agents. The widespread use of these agents mandates prospective, randomized evaluation of the cardiovascular safety of COX-2 inhibitors. |
format | Text |
id | pubmed-154429 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2003 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-1544292003-05-07 Cox-2: where are we in 2003? - Cardiovascular risk and Cox-2 inhibitors Mukherjee, Debabrata Topol, Eric J Arthritis Res Ther Commentary Selective cyclooxygenase-2 (COX-2) inhibitors were developed to reduce the gastrointestinal toxicity of conventional nonsteroidal anti-inflammatory agents. However, COX-2 inhibitors decrease prostacyclin production and may disrupt the normal homeostatic balance, leading to a prothrombotic state and offsetting the potential gastrointestinal benefits. Available clinical data and basic biological studies raise significant concern about the potential prothrombotic effect of this class of drugs. Two recent studies with a newer, more selective COX-2 inhibitor have added to the already existing concern about the cardiovascular safety of these agents. The widespread use of these agents mandates prospective, randomized evaluation of the cardiovascular safety of COX-2 inhibitors. BioMed Central 2003 2002-10-28 /pmc/articles/PMC154429/ /pubmed/12716442 http://dx.doi.org/10.1186/ar609 Text en Copyright © 2003 BioMed Central Ltd |
spellingShingle | Commentary Mukherjee, Debabrata Topol, Eric J Cox-2: where are we in 2003? - Cardiovascular risk and Cox-2 inhibitors |
title | Cox-2: where are we in 2003? - Cardiovascular risk and Cox-2 inhibitors |
title_full | Cox-2: where are we in 2003? - Cardiovascular risk and Cox-2 inhibitors |
title_fullStr | Cox-2: where are we in 2003? - Cardiovascular risk and Cox-2 inhibitors |
title_full_unstemmed | Cox-2: where are we in 2003? - Cardiovascular risk and Cox-2 inhibitors |
title_short | Cox-2: where are we in 2003? - Cardiovascular risk and Cox-2 inhibitors |
title_sort | cox-2: where are we in 2003? - cardiovascular risk and cox-2 inhibitors |
topic | Commentary |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC154429/ https://www.ncbi.nlm.nih.gov/pubmed/12716442 http://dx.doi.org/10.1186/ar609 |
work_keys_str_mv | AT mukherjeedebabrata cox2wherearewein2003cardiovascularriskandcox2inhibitors AT topolericj cox2wherearewein2003cardiovascularriskandcox2inhibitors |