Acute coronary syndromes: Virchow's triad revisited

被引:32
作者
Lee, KW [1 ]
Lip, GYH [1 ]
机构
[1] Univ Birmingham, City Hosp, Dept Med, Haemostasis Thrombosis & Vasc Biol Unit, Birmingham B18 7QH, W Midlands, England
关键词
acute coronary syndrome; unstable angina; thrombus;
D O I
10.1097/00001721-200310000-00001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The acute coronary syndromes (ACS), which include unstable angina, non-ST-segment and ST-segment elevation acute myocardial infarction, all share common pathophysiology processes that are characterized by coronary plaque disruption with superimposed thrombus formation, leading to myocardial ischaemia. A greater understanding of these processes has enable us to correlate the abnormalities in arterial vessel wall substrates ('vessel abnormalities'), rheologic and biomechanical conditions ('abnormal flow'), and blood thrombogenicity ('abnormal blood constituents') to the contribution of coronary plaque disruption and subsequent thrombosis, with the basic concepts of Virchow's triad for thrombus formation (thrombogenesis) described about 150 years ago. This improved understanding has led to the identification of newer therapeutic targets and, hence, novel pharmacological agents targeting different components of Virchow's triad, particularly in altering thrombus formation and plaque vulnerability.
引用
收藏
页码:605 / 625
页数:21
相关论文
共 242 条
[71]  
FRINK RJ, 1994, J INVASIVE CARDIOL, V6, P173
[72]  
Fuster V, 1998, Vasc Med, V3, P231, DOI 10.1177/1358836X9800300310
[73]   Matrix metalloproteinases in vascular remodeling and atherogenesis - The good, the bad, and the ugly [J].
Galis, ZS ;
Khatri, JJ .
CIRCULATION RESEARCH, 2002, 90 (03) :251-262
[74]   MICROSCOPIC LOCALIZATION OF ACTIVE PROTEASES BY IN-SITU ZYMOGRAPHY - DETECTION OF MATRIX METALLOPROTEINASE ACTIVITY IN VASCULAR TISSUE [J].
GALIS, ZS ;
SUKHOVA, GK ;
LIBBY, P .
FASEB JOURNAL, 1995, 9 (10) :974-980
[75]   Cerivastatin, an inhibitor of HMG-CoA reductase, inhibits urokinase/urokinase-receptor expression and MMP-9 secretion by peripheral blood monocytes -: A possible protective mechanism against atherothrombosis [J].
Ganné, F ;
Vasse, M ;
Beaudeux, JL ;
Peynet, J ;
François, A ;
Mishal, Z ;
Chartier, A ;
Tobelem, G ;
Vannier, JP ;
Soria, J ;
Soria, C .
THROMBOSIS AND HAEMOSTASIS, 2000, 84 (04) :680-688
[76]   ACUTE MYOCARDIAL-INFARCTION TRIGGERED BY EMOTIONAL-STRESS [J].
GELERNT, MD ;
HOCHMAN, JS .
AMERICAN JOURNAL OF CARDIOLOGY, 1992, 69 (17) :1512-1513
[77]   Fas is expressed in human atherosclerotic intima and promotes apoptosis of cytokine-primed human vascular smooth muscle cells [J].
Geng, YJ ;
Henderson, LE ;
Levesque, EB ;
Muszynski, M ;
Libby, P .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1997, 17 (10) :2200-2208
[78]   Therapeutic potential of matrix metalloproteinase inhibitors in atherosclerosis [J].
George, SJ .
EXPERT OPINION ON INVESTIGATIONAL DRUGS, 2000, 9 (05) :993-1007
[79]   HEMODYNAMIC SHEAR FORCE IN RUPTURE OF CORONARY ARTERIAL ATHEROSCLEROTIC PLAQUES [J].
GERTZ, SD ;
ROBERTS, WC .
AMERICAN JOURNAL OF CARDIOLOGY, 1990, 66 (19) :1368-1372
[80]   Tissue factor on the loose [J].
Giesen, PLA ;
Nemerson, V .
SEMINARS IN THROMBOSIS AND HEMOSTASIS, 2000, 26 (04) :379-384