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
  • [91] RESTENOSIS AFTER CORONARY ANGIOPLASTY - POTENTIAL BIOLOGIC DETERMINANTS AND ROLE OF INTIMAL HYPERPLASIA
    LIU, MW
    ROUBIN, GS
    KING, SB
    [J]. CIRCULATION, 1989, 79 (06) : 1374 - 1387
  • [92] IMMUNOHISTOCHEMICAL AND BIOCHEMICAL-EVIDENCE FOR A CARDIOVASCULAR MINERALOCORTICOID RECEPTOR
    LOMBES, M
    OBLIN, ME
    GASC, JM
    BAULIEU, EE
    FARMAN, N
    BONVALET, JP
    [J]. CIRCULATION RESEARCH, 1992, 71 (03) : 503 - 510
  • [93] INHIBITION OF MYOINTIMAL PROLIFERATION OF THE RAT CAROTID-ARTERY BY THE PEPTIDES, ANGIOPEPTIN AND BIM-23034
    LUNDERGAN, C
    FOEGH, ML
    VARGAS, R
    EUFEMIO, M
    BORMES, GW
    KOT, PA
    RAMWELL, PW
    [J]. ATHEROSCLEROSIS, 1989, 80 (01) : 49 - 55
  • [94] LUNDERGAN CF, 1991, J AM COLL CARDIOL, V17, pB132
  • [95] HEPARIN AND RELATED GLYCOSAMINOGLYCANS MODULATE THE SECRETORY PHENOTYPE OF VASCULAR SMOOTH-MUSCLE CELLS
    MAJACK, RA
    BORNSTEIN, P
    [J]. JOURNAL OF CELL BIOLOGY, 1984, 99 (05) : 1688 - 1695
  • [96] HEPARIN REGULATES SMOOTH-MUSCLE S-PHASE ENTRY IN THE INJURED RAT CAROTID-ARTERY
    MAJESKY, MW
    SCHWARTZ, SM
    CLOWES, MM
    CLOWES, AW
    [J]. CIRCULATION RESEARCH, 1987, 61 (02) : 296 - 300
  • [97] TISSUE FACTOR IS RAPIDLY INDUCED IN ARTERIAL SMOOTH-MUSCLE AFTER BALLOON INJURY
    MARMUR, JD
    ROSSIKHINA, M
    GUHA, A
    FYFE, B
    FRIEDRICH, V
    MENDLOWITZ, M
    NEMERSON, Y
    TAUBMAN, MB
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1993, 91 (05) : 2253 - 2259
  • [98] THROMBIN STIMULATES PROLIFERATION OF CULTURED RAT AORTIC SMOOTH-MUSCLE CELLS BY A PROTEOLYTICALLY ACTIVATED RECEPTOR
    MCNAMARA, CA
    SAREMBOCK, IJ
    GIMPLE, LW
    FENTON, JW
    COUGHLIN, SR
    OWENS, GK
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1993, 91 (01) : 94 - 98
  • [99] MIANO JM, 1993, AM J PATHOL, V142, P715
  • [100] MIANO JM, 1990, AM J PATHOL, V137, P761