Thrombin-activatable fibrinolysis inhibitor (TAFI): a novel predictor of angiographic coronary restenosis

被引:20
作者
Lau, HK
Segev, A
Hegele, RA
Sparkes, JD
Teitel, JM
Chisholm, RJ
Strauss, BH
机构
[1] Terrence Donnelly Heart Ctr, Roy & Ann Foss Cardiovasc Res Program, Toronto, ON, Canada
[2] Univ Toronto, St Michaels Hosp, Div Hematol & Oncol, Toronto, ON M5B 1W8, Canada
[3] John P Robarts Res Inst, London, ON, Canada
关键词
TAFI; PAI-I; restenosis; fibrinolysis;
D O I
10.1160/TH03-05-0308
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The fibrinolytic system is closely related to several processes that are involved in restenosis. We previously showed that low PAI-I plasma levels predicted restenosis. Recently, a different fibrinolytic inhibitor, TAFI, has been described. The aims of this study were to evaluate the relationship between pre-procedural plasma levels of TAFI and late angiographic restenosis and the interaction between TAFI and PAI-I. We prospectively studied 159 patients with stable angina who underwent successful elective angioplasty or stenting of de novo native coronary artery lesions. TAFI and PAI-I antigen levels were measured in plasma samples drawn before the procedure. Follow-up coronary angiography was performed in 92% of patients. There was a significant correlation between pre-procedural TAFI levels and 6-month % diameter stenosis (DS) (r = 0.21; p = 0.013). The overall angiographic restenosis rate (DS>50%) was 31%. Pre-procedural TAFI levels were significantly higher in patients with restenosis (108 +/- 33% versus 94 +/- 30%, p = 0.011). Restenosis rates for patients in the upper tertile of TAFI levels were 2-fold higher than for those in the lowest tertile (45% versus 22%; p = 0.016). A combination of high TAFI and low PAI-I levels identified patients at the highest risk of restenosis (53%) compared to 14% in patients with low TAFInd high PAI-I levels; p = 0.027. In conclusion, pre-procedural plasma TAFI antigen levels identify patients at increased risk for restenosis after PCI.
引用
收藏
页码:1187 / 1191
页数:5
相关论文
共 30 条
[1]   TAFI, or plasma procarboxypeptidase B, couples the coagulation and fibrinolytic cascades through the thrombin-thrombomodulin complex [J].
Bajzar, L ;
Morser, J ;
Nesheim, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (28) :16603-16608
[2]   PURIFICATION AND CHARACTERIZATION OF TAFI, A THROMBIN-ACTIVABLE FIBRINOLYSIS INHIBITOR [J].
BAJZAR, L ;
MANUEL, R ;
NESHEIM, ME .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (24) :14477-14484
[3]   Thrombin activatable fibrinolysis inhibitor and an antifibrinolytic pathway [J].
Bajzar, L .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2000, 20 (12) :2511-2518
[4]   Characterization of the gene encoding human TAFI (thrombin-activable fibrinolysis inhibitor; plasma procarboxypeptidase B) [J].
Boffa, MB ;
Reid, TS ;
Joo, E ;
Nesheim, ME ;
Koschinsky, ML .
BIOCHEMISTRY, 1999, 38 (20) :6547-6558
[5]   Biological profiles in subjects with recurrent acute coronary events compared with subjects with long-standing stable angina [J].
Bogaty, P ;
Poirier, P ;
Simard, S ;
Boyer, L ;
Solymoss, S ;
Dagenais, GR .
CIRCULATION, 2001, 103 (25) :3062-3068
[6]  
EATON DL, 1991, J BIOL CHEM, V266, P21833
[7]   QUANTITATIVE CORONARY ANGIOGRAPHY (QCA) IN INTERVENTIONAL CARDIOLOGY - CLINICAL-APPLICATION OF QCA MEASUREMENTS [J].
FOLEY, DP ;
ESCANED, J ;
STRAUSS, BH ;
DIMARIO, C ;
HAASE, J ;
KEANE, D ;
HERMANS, WRM ;
RENSING, BJ ;
DEFEYTER, PJ ;
SERRUYS, PW .
PROGRESS IN CARDIOVASCULAR DISEASES, 1994, 36 (05) :363-384
[8]   Prospective study of fibrinolytic factors and incident coronary heart disease - The Atherosclerosis Risk in Communities (ARIC) Study [J].
Folsom, AR ;
Aleksik, N ;
Park, E ;
Salomaa, V ;
Juneja, H ;
Wu, KK .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2001, 21 (04) :611-617
[9]  
HENDRIKS D, 1989, J CLIN CHEM CLIN BIO, V27, P277
[10]   Identification of polymorphisms in the promoter and the 3′ region of the TAFI gene:: evidence that plasma TAFI antigen levels are strongly genetically controlled [J].
Henry, M ;
Aubert, H ;
Morange, PE ;
Nanni, I ;
Alessi, MC ;
Tiret, L ;
Juhan-Vague, I .
BLOOD, 2001, 97 (07) :2053-2058