Markers of coagulation activation, endothelial stimulation and inflammation in patients with peripheral arterial disease

被引:76
作者
Cassar, K
Bachoo, P
Ford, I
Greaves, M
Brittenden, J
机构
[1] Aberdeen Royal Infirm, Vasc Unit, Aberdeen AB25 2ZN, Scotland
[2] Univ Aberdeen, Dept Vasc Surg, Aberdeen, Scotland
[3] Univ Aberdeen, Dept Med & Therapeut, Aberdeen, Scotland
关键词
haemostasis; thrombosis and vascular biology; peripheral arterial disease;
D O I
10.1016/j.ejvs.2004.11.001
中图分类号
R61 [外科手术学];
学科分类号
摘要
Objectives. Patients with peripheral arterial disease have a significantly increased risk of cardiovascular and cerebrovascular mortality. Studies have shown that some haemostatic and inflammatory markers are elevated in these patients but the effect of the severity of the disease has not been fully documented. The aim of this study was to assess the level of coagulation activation, endothelial stimulation and inflammation in patients with claudication and critical limb ischaemia (CLI) compared to healthy controls. Design and methods. A prospective observational study was conducted amongst 202 subjects: 132 claudicants, 30 patients with critical ischaemia, and 40 controls. D-dimer (DD) and thrombin-antithrombin III (TAT) levels measured using ELISA as markers of coagulation activation. von Willebrand factor (vWF) and high-sensitivity C-reactive protein (CRP) levels were measured as markers of endothelial and inflammatory stimulation. Results, vWF and CRP levels were significantly higher in patients with intermittent claudication (1.9 U/ml, range 0.78-4.05; p < 0.001; 3.4 mg/l, range 0.15-24; p > 0.001, respectively) and critical ischaemia (2.36 U/ml; range 1.03-5.69; p < 0.001; 7.17 mg/ml, range 0.15-174; p < 0.001, respectively) compared to controls (1.28 U/ml, range 0.62-3.13; 1.04, range 0.15-7.59 mg/l). DD was also significantly higher in claudicants (48.6 mug/ml; range 2-1741; p < 0.001) and in patients with CLI (61.1 mug/ml, range 3.65-1963; p < 0.001) compared to controls (26.1 mug/ml, range 9.65-203.1). TAT levels were significantly higher in CLI (3.14 mg/l, range 2.09-58.11), compared to controls (2.36 mg/l, range 1.49-7.38; p = 0.004). Patients with CLI had significantly higher levels of CRP, vWF, and TAT than claudicants. Conclusions. Coagulation activation and endothelial stimulation arc significantly increased ill patients with peripheral arterial disease compared to healthy controls. Coagulation and endothelial activation increases with the severity of the arterial disease.
引用
收藏
页码:171 / 176
页数:6
相关论文
共 33 条
[1]  
Baigent C, 2002, BMJ-BRIT MED J, V324, P71, DOI 10.1136/bmj.324.7329.71
[2]   Need to test the arterial inflammation hypothesis [J].
Bhatt, DL ;
Topol, EJ .
CIRCULATION, 2002, 106 (01) :136-140
[3]   THE ACUTE INFLUENCE OF SMOKING ON THE ENDOTHELIUM [J].
BLANN, AD .
ATHEROSCLEROSIS, 1992, 96 (2-3) :249-250
[4]  
BLANN AD, 1993, J HUM HYPERTENS, V7, P107
[5]   The effect of peripheral percutaneous transluminal angioplasty on quality of life in patients with intermittent claudication [J].
Cassar, K ;
Bachoo, P ;
Brittenden, J .
EUROPEAN JOURNAL OF VASCULAR AND ENDOVASCULAR SURGERY, 2003, 26 (02) :130-136
[6]   The role of platelets in peripheral vascular disease [J].
Cassar, K ;
Bachoo, P ;
Brittenden, J .
EUROPEAN JOURNAL OF VASCULAR AND ENDOVASCULAR SURGERY, 2003, 25 (01) :6-15
[7]  
Chesebro JH, 1997, HAEMOSTASIS, V27, P12
[8]   THE PREVALENCE OF PERIPHERAL ARTERIAL-DISEASE IN A DEFINED POPULATION [J].
CRIQUI, MH ;
FRONEK, A ;
BARRETTCONNOR, E ;
KLAUBER, MR ;
GABRIEL, S ;
GOODMAN, D .
CIRCULATION, 1985, 71 (03) :510-515
[9]  
Dormandy J, 1999, Semin Vasc Surg, V12, P123
[10]   Fibrinogen and von Willebrand factor in IDDM: Relationships to lipid vascular risk factors, blood pressure, glycaemic control and urinary albumin excretion rate: The EURODIAB IDDM complications study [J].
Greaves, M ;
Malia, RG ;
Goodfellow, K ;
Mattock, M ;
Stevens, LK ;
Stephenson, JM ;
Fuller, JH ;
Karamanos, B ;
Tountas, C ;
Kofinis, A ;
Petrou, K ;
Katsilambros, N ;
Giorgino, R ;
Cignarelli, M ;
DeCicco, ML ;
Ramunni, I ;
IonescuTirgoviste, C ;
Iosif, CM ;
Pitei, D ;
Buligescu, S ;
Tamas, G ;
Kerenyi, Z ;
Ahmed, AM ;
Toth, J ;
Kempler, P ;
Muntoni, S ;
Songini, M ;
Stabilini, M ;
Fossarello, M ;
Pintus, S ;
Ferriss, JB ;
Cronin, CC ;
Whyte, AE ;
Cleary, PE ;
Toeller, M ;
Klischan, A ;
Forst, T ;
Gries, FA ;
Rottiers, R ;
Priem, H ;
Ebeling, P ;
Sinisalo, M ;
Koivisto, VA ;
IdziorWalus, B ;
Solnica, B ;
SzopinskaCiba, L ;
Solnica, K ;
Krans, HMJ ;
Lemkes, HHPJ ;
Jansen, JJ .
DIABETOLOGIA, 1997, 40 (06) :698-705