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Research article summary (published 30 Jul 2009):

Selective cyclooxygenase-2 inhibition reduces endothelial dysfunction and improves inflammatory status in patients with intermittent claudication.

Full Abstract

INTRODUCTION AND OBJECTIVES: Both endothelial dysfunction and a proinflammatory state are present during the early stages of atherosclerosis. In this context, increased expression of cyclooxygenase-2 (COX-2) results in higher levels of vasoconstrictive and proinflammatory substances. The aim of this study was to investigate the influence of COX-2 activity on endothelial dysfunction associated with peripheral arterial disease (PAD). METHODS: Brachial artery flow-mediated dilatation (BAFMD), endothelin and high-sensitivity C-reactive protein (hsCRP) levels, and the lipid profile were assessed in 40 patients with intermittent claudication. Of these, 20 were randomly assigned to a group in which they received the selective COX-2 inhibitor celecoxib for 1 week (Group 1), while the other 20 served as controls (Group 2). RESULTS: In Group 1, BAFMD increased significantly both 3 hours after the first dose of celecoxib (3.33+/-4.11 vs. 6.97+/-3.27%; P=.008) and 1 week after (3.33+/-4.11 vs. 7.09+/-4.40%; P=.001). The endothelin level decreased significantly in Group 1 (2.92+/-1.87 vs. 1.93+/-1.07 pg/ ml; P=.018), as did the levels of hsCRP (4.78+/-2.73 vs. 2.95+/-2.11 mg/l; P=.023) and low-density lipoprotein cholesterol (106.38+/-18.89 vs. 90.8+/-28.58 mg/dl; P=.019). In Group 2, none of these parameters changed significantly. CONCLUSIONS: COX-2 products contribute to endothelial dysfunction and an inflammatory state in PAD. This study's findings provide evidence that these phenomena are implicated in the initiation of atherosclerosis and could prove a new means of investigating alternative approaches to the treatment of early-stage disease.

 

Author information

Author/s: Flórez, Aurora (A); de Haro, Joaquín (J); Martínez, Esther (E); Varela, César (C); Bleda, Silvia (S); Acín, Francisco (F);

Affiliation: Servicio de Angiología y Cirugía Vascular. Hospital Universitario de Getafe. Getafe. Madrid. España. aurora.florez(-atsign-)terra.es

Journal and publication information

Publication Type: Journal Article; Randomized Controlled Trial

Journal: Revista española de cardiología (Rev Esp Cardiol), published in Spain. (Language: eng)

Reference: 2009-Aug; vol 62 (issue 8) : pp 851-7

Dates: Created 2009/08/26; Completed 2009/10/30;

PMID: 19706240, status: MEDLINE (last retrieval date: 10/30/2009, IMS Date: )

Sourced from the National Library of Medicine. Abstract text and other information may be subject to copyright.

Comments and Corrections

CommentIn: Rev Esp Cardiol. 2009 Aug;62(8):839-42. (PMID: 19706237)

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MeSH headings (categories)

This article was linked to the MESH Headings shown below.

Associated Chemicals: Cyclooxygenase 2 Inhibitors (0) ; Pyrazoles (0) ; Sulfonamides (0) ; celecoxib (169590-42-5)

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