Plasma von Willebrand factor, thrombosis, and the endothelium: The first 30 years

被引:146
作者
Blann, AD [1 ]
机构
[1] Univ Birmingham, City Hosp, Dept Med, Haemostasis Thrombosis & Vasc Biol Unit, Birmingham B18 7QH, W Midlands, England
关键词
endothelium; vonWillebrand factor; thrombosis; atherosclerosis;
D O I
10.1160/TH05-07-0527
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
It is quite useless to argue the questions concerning the development of intimal scleroses if we study and discuss the late stages of the disease alone. If we wish to gain insight into the complex question of arterio-sclerosis we must attempt to follow the lesion from its earliest beginning (Klotz and Manning, J Path Bact 1911: 16; 211-20). Over thirty years ago Boneu and colleagues published a report of raised levels of plasma von Willebrand factor (vWf) in patients with arteritis, diabetes and sepsis. They concluded that raised levels of this molecule indicate endothelial damage, and may possibly be a contributory factor in thrombosis in arterial disease. The former aspect of this conclusion is now accepted, and numerous studies on the risk factors for atherosclerosis provide mechanisms for this damage. Other studies have demonstrated raised levels in cancer and in connective tissue disease. Numerous long-term follow-up studies have also demonstrated that increased vWf predicts major cardiovascular end points. However, the link between these studies, and the latter aspect of Boneu's conclusion, that raised vWf contributes to thrombosis is, although attractive, nevertheless unproven. Despite this, vWf remains the most important plasma marker of endothelial damage/dysfunction and as such attracts clinical attention.
引用
收藏
页码:49 / 55
页数:7
相关论文
共 109 条
[21]  
Blann AD, 1997, AM J HEMATOL, V55, P15, DOI 10.1002/(SICI)1096-8652(199705)55:1<15::AID-AJH3>3.0.CO
[22]  
2-6
[23]   Endothelial cell activation, injury, damage and dysfunction: separate entities or mutual terms? [J].
Blann, AD .
BLOOD COAGULATION & FIBRINOLYSIS, 2000, 11 (07) :623-630
[24]   CHANGES IN BLOOD-COAGULATION AND FIBRINOLYSIS IN PATIENTS ON DIFFERENT TREATMENT REGIMENS FOR PROSTATIC-CANCER - PREDICTORS FOR CARDIOVASCULAR COMPLICATIONS [J].
BLOMBACK, M ;
HEDLUND, PO ;
SAWE, U .
THROMBOSIS RESEARCH, 1988, 49 (01) :111-121
[25]  
BONEU B, 1975, LANCET, V1, P1430
[26]   AN INVITRO MODEL FOR THE STUDY OF ACUTE RELEASE OF VONWILLEBRAND-FACTOR FROM HUMAN-ENDOTHELIAL CELLS [J].
BOOTH, F ;
ALLINGTON, MJ ;
CEDERHOLMWILLIAMS, SA .
BRITISH JOURNAL OF HAEMATOLOGY, 1987, 67 (01) :71-78
[27]   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
[28]   BOWIE SYMPOSIUM ON VONWILLEBRANDS DISEASE .3. VONWILLEBRAND-FACTOR AND ANIMAL-MODELS - CONTRIBUTIONS TO GENE-THERAPY, THROMBOTIC THROMBOCYTOPENIC PURPURA, AND CORONARY-ARTERY THROMBOSIS [J].
BRINKHOUS, KM ;
REDDICK, RL ;
READ, MS ;
NICHOLS, TC ;
BELLINGER, DA ;
GRIGGS, TR .
MAYO CLINIC PROCEEDINGS, 1991, 66 (07) :733-742
[29]  
BRINKHOUS KM, 1970, THROMB DIATH HAEMO, V40, P1
[30]   Serum soluble vascular cell adhesion molecule-1: Role as a surrogate marker of angiogenesis [J].
Byrne, GJ ;
Ghellal, A ;
Iddon, J ;
Blann, AD ;
Venizelos, V ;
Kumar, S ;
Howell, A ;
Bundred, NJ .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2000, 92 (16) :1329-1336