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Effect of treatment with 5-lipoxygenase inhibitor VIA-2291 (atreleuton) on coronary plaque progression: a serial CT angiography study.

Authors :
Matsumoto S
Ibrahim R
Grégoire JC
L'Allier PL
Pressacco J
Tardif JC
Budoff MJ
Source :
Clinical cardiology [Clin Cardiol] 2017 Apr; Vol. 40 (4), pp. 210-215. Date of Electronic Publication: 2016 Nov 24.
Publication Year :
2017

Abstract

Background: Inflammation has a key role in the process of atherosclerosis. Production of leukotrienes by 5-lipoxygenase has been linked to atherosclerotic plaques and cardiovascular events.<br />Hypothesis: In this study, a selective 5-LO inhibitor will slow plaque progression using serial cardiac computed tomographic angiography (CCTA).<br />Methods: Patients with recent acute coronary syndrome (ACS) were prospectively assigned to one of 3 VIA-2291 doses (25 mg, 50 mg, 100 mg) or placebo by oral administration. All groups underwent CCTA at baseline and at 6 months' follow-up. Plaque types such as low-attenuation plaque (LAP), fibro-fatty tissue (FF), fibro-calcified plaque (FC), and dense calcium plaque (DC) were measured based upon predefined density threshold, and changes from baseline CCTA were analyzed.<br />Results: The final analysis included 54 patients (age, 56 ± 9 years; 85.1% male) with CCTA at baseline and 24 weeks. Evaluating on treatment VIA-2291 (all 3 doses, n = 37) demonstrated significant reductions in plaque progression compared with placebo (n = 17). VIA-2291 significantly reduced LAP (5.9 ± 20.7 mm <superscript>3</superscript> vs -9.7 ± 33.3 mm <superscript>3</superscript> ), FF (11.1 mm <superscript>3</superscript>  ± 13.3 mm <superscript>3</superscript> vs -0.9 ± 2.7 mm <superscript>3</superscript> ), and FC (-0.1 ± 6.22 mm <superscript>3</superscript> vs -14.3 ± 6.2 mm <superscript>3</superscript> ; all P < 0.05) and retarded the progression of DC (3.9 ± 3.2 mm <superscript>3</superscript> vs 0.2 ± 0.4 mm <superscript>3</superscript> ) compared with placebo.<br />Conclusions: VIA-2291 resulted in slowed plaque progression compared with placebo across different plaque subtypes in patients with recent ACS (http://ClinicalTrials.gov NCT00358826).<br /> (© 2016 Wiley Periodicals, Inc.)

Details

Language :
English
ISSN :
1932-8737
Volume :
40
Issue :
4
Database :
MEDLINE
Journal :
Clinical cardiology
Publication Type :
Academic Journal
Accession number :
27883201
Full Text :
https://doi.org/10.1002/clc.22646