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

Autor: Jean-Claude Tardif, Reda Ibrahim, Josephine Pressacco, Jean Grégoire, Suguru Matsumoto, Philippe L. L’Allier, Matthew J. Budoff
Rok vydání: 2017
Předmět:
Time Factors
Computed Tomography Angiography
030204 cardiovascular system & hematology
Cardiorespiratory Medicine and Haematology
Imaging
0302 clinical medicine
Clinical trials
Oral administration
Coronary plaque
80 and over
Medicine
Hydroxyurea
acute coronary syndromes
030212 general & internal medicine
Lipoxygenase Inhibitors
Prospective Studies
Plaque
Atherosclerotic
Aged
80 and over

medicine.diagnostic_test
General Medicine
Middle Aged
Coronary Vessels
Plaque
Atherosclerotic

Treatment Outcome
Atreleuton
Cardiology
Disease Progression
Radiology
medicine.symptom
Drug
Cardiology and Cardiovascular Medicine
Adult
medicine.medical_specialty
Acute coronary syndrome
Ischemic heart disease
Clinical Investigations
Inflammation
and over
Placebo
Dose-Response Relationship
03 medical and health sciences
Internal medicine
Multidetector Computed Tomography
Humans
Acute Coronary Syndrome
Aged
Dose-Response Relationship
Drug

business.industry
computed tomography
medicine.disease
Clinical trial
Cardiovascular System & Hematology
Angiography
business
Follow-Up Studies
Zdroj: Clinical cardiology, vol 40, iss 4
Matsumoto, S; Ibrahim, R; Gregoire, JC; L'Allier, PL; Pressacco, J; Tardif, J-C; et al.(2017). Effect of treatment with 5-lipoxygenase inhibitor VIA-2291 (atreleuton) on coronary plaque progression: a serial CT angiography study. CLINICAL CARDIOLOGY, 40(4), 210-215. doi: 10.1002/clc.22646. UCLA: Retrieved from: http://www.escholarship.org/uc/item/9f65w0rm
DOI: 10.1002/clc.22646.
Popis: 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. HYPOTHESIS: In this study, a selective 5‐LO inhibitor will slow plaque progression using serial cardiac computed tomographic angiography (CCTA). 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. 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(3) vs −9.7 ± 33.3 mm(3)), FF (11.1 mm(3) ± 13.3 mm(3) vs −0.9 ± 2.7 mm(3)), and FC (−0.1 ± 6.22 mm(3) vs −14.3 ± 6.2 mm(3); all P < 0.05) and retarded the progression of DC (3.9 ± 3.2 mm(3) vs 0.2 ± 0.4 mm(3)) compared with placebo. CONCLUSIONS: VIA‐2291 resulted in slowed plaque progression compared with placebo across different plaque subtypes in patients with recent ACS (http://ClinicalTrials.gov NCT00358826).
Databáze: OpenAIRE