RESTENOSIS AFTER CORONARY ANGIOPLASTY

被引:48
作者
HAMON, M
BAUTERS, C
MCFADDEN, EP
WERNERT, N
LABLANCHE, JM
DUPUIS, B
BERTRAND, ME
机构
[1] UNIV LILLE, DEPT CARDIOL, LILLE, FRANCE
[2] UNIV LILLE, DEPT PATHOL, LILLE, FRANCE
[3] UNIV LILLE, DEPT PHARMACOL, LILLE, FRANCE
关键词
CORONARY ANGIOPLASTY; RESTENOSIS; SMOOTH MUSCLE CELL; BALLOON DENUDATION;
D O I
10.1093/eurheartj/16.suppl_I.33
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The major disadvantage of using percutaneous transluminal coronary angioplasty to treat patients with atherosclerotic coronary disease is the frequent occurrence of restenosis after an initially successful procedure. Studies in animals and histological observations in man have demonstrated that restenosis is characterized by neointimal hyperplasia due to smooth muscle cell proliferation and to the synthesis of extracellular matrix. Improvements in technology or pharmacological interventions have had no significant impact on the rate of restenosis. In spite of our increased understanding of the molecular mechanisms of restenosis, no effective treatment is available at the present time. Gene therapy which has produced encouraging initial results in experimental models, may provide a solution in the medium term.
引用
收藏
页码:33 / 48
页数:16
相关论文
共 161 条
  • [1] CYTOKINES AND GROWTH-FACTORS POSITIVELY AND NEGATIVELY REGULATE INTERSTITIAL COLLAGEN GENE-EXPRESSION IN HUMAN VASCULAR SMOOTH-MUSCLE CELLS
    AMENTO, EP
    EHSANI, N
    PALMER, H
    LIBBY, P
    [J]. ARTERIOSCLEROSIS AND THROMBOSIS, 1991, 11 (05): : 1223 - 1230
  • [2] LOW-DENSITY LIPOPROTEINS INHIBIT ENDOTHELIUM-DEPENDENT RELAXATION IN RABBIT AORTA
    ANDREWS, HE
    BRUCKDORFER, KR
    DUNN, RC
    JACOBS, M
    [J]. NATURE, 1987, 327 (6119) : 237 - 239
  • [3] AN ACTIVATED FORM OF TRANSFORMING GROWTH FACTOR-BETA IS PRODUCED BY COCULTURES OF ENDOTHELIAL-CELLS AND PERICYTES
    ANTONELLIORLIDGE, A
    SAUNDERS, KB
    SMITH, SR
    DAMORE, PA
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (12) : 4544 - 4548
  • [4] DOES NITRIC-OXIDE INHIBIT SMOOTH-MUSCLE PROLIFERATION
    ASSENDER, JW
    SOUTHGATE, KM
    NEWBY, AC
    [J]. JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 1991, 17 : S104 - S107
  • [5] CELLULAR-TRANSFORMATION BY COORDINATED ACTION OF 3 PEPTIDE GROWTH-FACTORS FROM HUMAN-PLATELETS
    ASSOIAN, RK
    GROTENDORST, GR
    MILLER, DM
    SPORN, MB
    [J]. NATURE, 1984, 309 (5971) : 804 - 806
  • [6] HEPARIN INHIBITS COLLAGENASE GENE-EXPRESSION MEDIATED BY PHORBOL ESTER-RESPONSIVE ELEMENT IN PRIMATE ARTERIAL SMOOTH-MUSCLE CELLS
    AU, YPT
    MONTGOMERY, KF
    CLOWES, AW
    [J]. CIRCULATION RESEARCH, 1992, 70 (05) : 1062 - 1069
  • [7] INTIMAL PROLIFERATION OF SMOOTH-MUSCLE CELLS AS AN EXPLANATION FOR RECURRENT CORONARY-ARTERY STENOSIS AFTER PERCUTANEOUS TRANS-LUMINAL CORONARY ANGIOPLASTY
    AUSTIN, GE
    RATLIFF, NB
    HOLLMAN, J
    TABEI, S
    PHILLIPS, DF
    [J]. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1985, 6 (02) : 369 - 375
  • [8] BALCON R, 1992, CIRCULATION, V86, P100
  • [9] INSULIN, INSULIN-LIKE GROWTH FACTOR-I AND PLATELET-DERIVED GROWTH-FACTOR INTERACT ADDITIVELY IN THE INDUCTION OF THE PROTOONCOGENE C-MYC AND CELLULAR PROLIFERATION IN CULTURED BOVINE AORTIC SMOOTH-MUSCLE CELLS
    BANSKOTA, NK
    TAUB, R
    ZELLNER, K
    KING, GL
    [J]. MOLECULAR ENDOCRINOLOGY, 1989, 3 (08) : 1183 - 1190
  • [10] BASSOLS A, 1988, J BIOL CHEM, V263, P3039