Effect of Atorvastatin (80 mg/day) versus Pravastatin (40 mg/day) on arterial remodeling at coronary branch points (from the REVERSAL study)

被引:16
作者
Nicholls, SJ [1 ]
Tuzcu, EM [1 ]
Schoenhagen, P [1 ]
Sipahi, I [1 ]
Crowe, T [1 ]
Kapadia, S [1 ]
Nissen, SE [1 ]
机构
[1] Cleveland Clin Fdn, Dept Cardiovasc Med, Cleveland, OH 44195 USA
关键词
D O I
10.1016/j.amjcard.2005.07.085
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The effect of moderate and intensive lipid lowering on plaque progression and arterial remodeling at coronary branch points was investigated. Intensive (+ 1 +/- 19.6%), but not moderate (+ 4.1 +/- 15.1%), lipid lowering prevented an increase in plaque area at the branch points. The 2 strategies were associated with increased areas of the lumen (+7.6% to 9.4%) and external elastic membrane (+9.6% to 10.8%). In contrast, there was no significant change in plaque, lumen, and/or external elastic membrane areas at the nonbranch point site. These results suggest that intensive lipid lowering can have a dramatic effect on atheroma-prone regions and that remodeling in response to changes in plaque is a heterogenous process. (C) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:1636 / 1639
页数:4
相关论文
共 9 条
[1]   Gene expression profiling of vascular endothelial cells exposed to fluid mechanical forces: Relevance for focal susceptibility to atherosclerosis [J].
Brooks, AR ;
Lelkes, PI ;
Rubanyi, GM .
ENDOTHELIUM-JOURNAL OF ENDOTHELIAL CELL RESEARCH, 2004, 11 (01) :45-57
[2]   COMPENSATORY ENLARGEMENT OF HUMAN ATHEROSCLEROTIC CORONARY-ARTERIES [J].
GLAGOV, S ;
WEISENBERG, E ;
ZARINS, CK ;
STANKUNAVICIUS, R ;
KOLETTIS, GJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1987, 316 (22) :1371-1375
[3]   Endothelial function and coronary artery disease [J].
Kinlay, S ;
Libby, P ;
Ganz, P .
CURRENT OPINION IN LIPIDOLOGY, 2001, 12 (04) :383-389
[4]   FOCAL COMPENSATORY ENLARGEMENT OF HUMAN ARTERIES IN RESPONSE TO PROGRESSIVE ATHEROSCLEROSIS - IN-VIVO DOCUMENTATION USING INTRAVASCULAR ULTRASOUND [J].
LOSORDO, DW ;
ROSENFIELD, K ;
KAUFMAN, J ;
PIECZEK, A ;
ISNER, JM .
CIRCULATION, 1994, 89 (06) :2570-2577
[5]   EARLY EVIDENCE OF ENDOTHELIAL VASODILATOR DYSFUNCTION AT CORONARY BRANCH-POINTS [J].
MCLENACHAN, JM ;
VITA, J ;
FISH, RD ;
TREASURE, CB ;
COX, DA ;
GANZ, P ;
SELWYN, AP .
CIRCULATION, 1990, 82 (04) :1169-1173
[6]   Effect of intensive compared with moderate lipid-lowering therapy on progression of coronary atherosclerosis - A randomized controlled trial [J].
Nissen, SE ;
Tuzcu, EM ;
Schoenhagen, P ;
Brown, BG ;
Ganz, P ;
Vogel, RA ;
Crowe, T ;
Howard, G ;
Cooper, CJ ;
Brodie, B ;
Grines, CL ;
DeMaria, AN .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2004, 291 (09) :1071-1080
[7]   Early statin treatment in patients with acute coronary syndrome - Demonstration of the beneficial effect on atherosclerotic lesions by serial volumetric intravascular ultrasound analysis during half a year after coronary event: The ESTABLISH study [J].
Okazaki, S ;
Yokoyama, T ;
Miyauchi, K ;
Shimada, K ;
Kurata, T ;
Sato, H ;
Daida, H .
CIRCULATION, 2004, 110 (09) :1061-1068
[8]   PARADOXICAL ARTERIAL-WALL SHRINKAGE MAY CONTRIBUTE TO LUMINAL NARROWING OF HUMAN ATHEROSCLEROTIC FEMORAL ARTERIES [J].
PASTERKAMP, G ;
WENSING, PJW ;
POST, MJ ;
HILLEN, B ;
MALI, WPTM ;
BORST, C .
CIRCULATION, 1995, 91 (05) :1444-1449
[9]   Fluid mechanics of vascular systems, diseases, and thrombosis [J].
Wootton, DM ;
Ku, DN .
ANNUAL REVIEW OF BIOMEDICAL ENGINEERING, 1999, 1 :299-329