Von Willebrand factor in cardiovascular disease focus on acute coronary syndromes

被引:340
作者
Spiel, Alexander O. [1 ]
Gilbert, James C. [2 ]
Jilma, Bernd [1 ]
机构
[1] Med Univ Vienna, Dept Clin Pharmacol, A-1090 Vienna, Austria
[2] Archemix Corp, Cambridge, MA USA
关键词
coronary disease; myocardial infarction; platelets; thrombosis von Willebrand factor;
D O I
10.1161/CIRCULATIONAHA.107.722827
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
von Willebrand factor (VWF) plays a pivotal role in platelet adhesion and aggregation at sites of high shear rates (eg, in coronary arteries that have stenotic or ruptured atherosclerotic plaque lesions). Numerous studies have investigated the relationship between VWF plasma levels and thromboembolic cardiovascular events. In contrast to the rather weak association in the general population, in patients with preexisting vascular disease, VWF is significantly predictive for adverse cardiac events, including death. Likewise, VWF typically rises during the course of acute coronary syndrome, and the extent of this VWF release is an independent predictor of adverse clinical outcome in these patients. Various lines of evidence indicate that VWF is not only a marker but also actually an important effector in the pathogenesis of myocardial infarction. This central role of VWF in thrombogenesis has made it a promising target for research into new antiplatelet therapies that specifically inhibit VWF. This review focuses on the role of VWF in acute coronary syndrome and further outlines the relevance of therapeutic interventions targeting VWF for acute coronary syndrome patients.
引用
收藏
页码:1449 / 1459
页数:11
相关论文
共 144 条
[1]   TREATMENT OF VONWILLEBRANDS DISEASE [J].
ALEDORT, LM .
MAYO CLINIC PROCEEDINGS, 1991, 66 (08) :841-846
[2]   ACC/AHA 2007 Guidelines for the Management of Patients With unstable Angina/Non-ST-Elevation Myocardial Infarction A Report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines (Writing Committee to Revise the 2002 Guidelines for the Management of Patients With Unstable Angina/Non-ST-Elevation Myocardial Infarction) Developed in Collaboration with the American College of Emergency Physicians, the Society for Cardiovascular Angiography and Interventions, and the Society of Thoracic Surgeons Endorsed by the American Association of Cardiovascular and Pulmonary Rehabilitation and the Society for Academic Emergency Medicine [J].
Anderson, Jeffrey L. ;
Adams, Cynthia D. ;
Antman, Elliott M. ;
Bridges, Charles R. ;
Califf, Robert M. ;
Casey, Donald E., Jr. ;
Chavey, William E. ;
Fesmire, Francis M. ;
Hochman, Judith S. ;
Levin, Thomas N. ;
Lincoff, A. Michael ;
Peterson, Eric D. ;
Theroux, Pierre ;
Wenger, Nanette Kass ;
Wright, R. Scott ;
Smith, Sidney C. ;
Jacobs, Alice K. ;
Halperin, Jonathan L. ;
Hunt, Sharon A. ;
Krumholz, Harlan M. ;
Kushner, Frederick G. ;
Lytle, Bruce W. ;
Nishimura, Rick ;
Ornato, Joseph P. ;
Page, Richard L. ;
Riegel, Barbara .
CIRCULATION, 2007, 116 (07) :E148-E304
[3]   EARLY CORONARY REPERFUSION BLUNTS THE PROCOAGULANT RESPONSE OF PLASMINOGEN-ACTIVATOR INHIBITOR-1 AND VONWILLEBRAND-FACTOR IN ACUTE MYOCARDIAL-INFARCTION [J].
ANDREOTTI, F ;
RONCAGLIONI, MC ;
HACKETT, DR ;
KHAN, MI ;
REGAN, T ;
HAIDER, AW ;
DAVIES, GJ ;
KLUFT, C ;
MASERI, A .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1990, 16 (07) :1553-1560
[4]  
ANDREOTTI F, 1992, THROMB HAEMOSTASIS, V68, P678
[5]   Collagen-bound von Willebrand factor has reduced affinity for factor VIII [J].
Bendetowicz, AV ;
Wise, RJ ;
Gilbert, GE .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (18) :12300-12307
[6]   FREE-RADICALS, ANTIOXIDANTS, AND ENDOTHELIAL-CELL DAMAGE AFTER PERCUTANEOUS TRANSLUMINAL CORONARY ANGIOPLASTY [J].
BLANN, A ;
MIDGLEY, H ;
BURROWS, G ;
MAXWELL, S ;
UTTING, S ;
DAVIES, M ;
WAITE, M ;
MCCOLLUM, C .
CORONARY ARTERY DISEASE, 1993, 4 (10) :905-910
[7]  
BLANN A, 1993, BRIT J BIOMED SCI, V50, P125
[8]  
BOND L, 1988, NEW ENGL J MED, V318, P121
[9]   Shielding the front-strand β3 of the !von Willebrand factor A1 domain inhibits its binding to platelet glycoprotein Ibα [J].
Bonnefoy, A ;
Yamamoto, H ;
Thys, C ;
Kito, M ;
Vermylen, J ;
Hoylaerts, MF .
BLOOD, 2003, 101 (04) :1375-1383
[10]   TRANSPLANTATION OF NORMAL BONE-MARROW INTO A PIG WITH SEVERE VONWILLEBRANDS DISEASE [J].
BOWIE, EJW ;
SOLBERG, LA ;
FASS, DN ;
JOHNSON, CM ;
KNUTSON, GJ ;
STEWART, ML ;
ZOECKLEIN, LJ .
JOURNAL OF CLINICAL INVESTIGATION, 1986, 78 (01) :26-30