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Virtual histology evaluation of atherosclerosis regression during atorvastatin and ezetimibe administration: HEAVEN study
T. Kovarnik, GS. Mintz, H. Skalicka, A. Kral, J. Horak, R. Skulec, J. Uhrova, P. Martasek, RW. Downe, A. Wahle, M. Sonka, V. Mrazek, M. Aschermann, A. Linhart,
Language English Country Japan
Document type Journal Article, Randomized Controlled Trial, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't
NLK
Free Medical Journals
from 2002
J-STAGE (Japan Science & Technology Information Aggregator, Electronic) - English
from 2002
J-STAGE (Japan Science & Technology Information Aggregator, Electronic) Freely Available Titles - English
from 2002
Open Access Digital Library
from 2002-01-01
- MeSH
- Anticholesteremic Agents therapeutic use MeSH
- Plaque, Atherosclerotic drug therapy pathology ultrasonography MeSH
- Azetidines therapeutic use MeSH
- Cholesterol metabolism MeSH
- Ultrasonography, Interventional MeSH
- Single-Blind Method MeSH
- Drug Therapy, Combination MeSH
- Coronary Vessels metabolism pathology ultrasonography MeSH
- Heptanoic Acids therapeutic use MeSH
- Middle Aged MeSH
- Humans MeSH
- Lipoproteins metabolism MeSH
- Cell Adhesion Molecules metabolism MeSH
- Coronary Artery Disease drug therapy pathology ultrasonography MeSH
- Disease Progression MeSH
- Pyrroles therapeutic use MeSH
- Aged MeSH
- Treatment Outcome MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Randomized Controlled Trial MeSH
- Research Support, N.I.H., Extramural MeSH
BACKGROUND: There is no study focusing on changes in coronary atherosclerosis during dual lipid-lowering therapy with statin and ezetimibe. METHODS AND RESULTS: Eighty-nine patients with stable angina randomized in a 1:1 ratio to Group A (aggressive therapy: atorvastatin 80mg, ezetimibe 10mg) and Group S (standard therapy) were analyzed. Treatment period was 12 months. Coronary arteries were examined by intravascular ultrasound and virtual histology. We found a decrease in the percent atheroma volume (PAV) (-0.4%) in Group A compared with an increase (+1.4%) in Group S (P=0.014) and this was accompanied by an increased frequency of combined atherosclerosis regression (increased lumen volume+decreased PAV) in group A (40.5%) compared with group S (14.9%) (P=0.007). The target low-density lipoprotein cholesterol level <2mmol/L, presence of at least 4 of 5 atherosclerotic risk factors, and decreased level of vascular cellular adhesive molecule were independent predictors of plaque regression. There were no significant differences in plaque composition between the 2 groups over the study duration. However, during analysis of the 2 groups together, fibrous and fibro-fatty tissues decreased and dense calcification and necrotic core increased during follow-up. CONCLUSIONS: Dual lipid-lowering therapy starts atherosclerosis regression, but does not lead to significant changes in plaque composition. The continuous shift in plaque from fibro and fibro-fatty to necrotic with calcification was present in both groups.
References provided by Crossref.org
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