P-selectin/PSGL-1 Inhibitors versus enoxaparin in the resolution of venous thrombosis: A meta-analysis

被引:40
作者
Ramacciotti, Eduardo [1 ]
Myers, Daniel D., Jr. [2 ]
Wrobleski, Shirley K.
Deatrick, K. Barry
Londy, Frank J. [3 ]
Rectenwald, John E.
Henke, Peter K.
Schaub, Robert G. [4 ]
Wakefield, Thomas W.
机构
[1] Univ Michigan, Sch Med, Vasc Surg Sect, Jobst Vasc Surg Res Lab,Cardiovasc Ctr, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Unit Lab Anim Med, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Dept Radiol, Ann Arbor, MI 48109 USA
[4] Archemix Corp, Cambridge, MA USA
关键词
P-selectin; inflammation; venous thrombosis; enoxaparin; animal model; meta-analysis; SOLUBLE P-SELECTIN; THROMBOEMBOLISM; RISK; ANTICOAGULATION; COAGULATION; LEUKOCYTES; HEPARINS; DISEASE; MODEL; WALL;
D O I
10.1016/j.thromres.2009.10.022
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: P-selectin antagonism has been shown to decrease thrombogenesis and inflammation in animal models of deep venous thrombosis (DVT). Objective: To determine the effectiveness of P-selectin inhibitors versus saline and enoxaparin in venous thrombus resolution in nonhuman primate models of venous thrombosis. Methods: Studies reporting vein re-opening, inflammation expressed as Gadolinium enhancement and coagulation parameters were searched in the literature and pooled into a meta-analysis using an inverse variance with random effects. Results: Five studies were identified comparing P-selectin/ PSGL-1 inhibitors versus saline or enoxaparin regarding venous thrombosis resolution. Vein re-opening was significantly higher on P-selectin/ PSGL-1 compounds, when compared to saline (Inverse Variance [IV] 95% CI; 44.37 [17.77-70.96], p = 0.001, I(2) = 97%) and similar to enoxaparin (IV 95% CI; 5.03 [-8.88-18.95], p = 0.48, I(2) = 41%). Inflammation, reflected as Gadolinium enhancement at magnetic resonance venography (MRV), was significantly decreased in the P-selectin treated group when compared to saline (IV 95% CI; -17.84 [-14.98--8.30], p<0.00001, I(2) = 80%). No significant differences on vein wall inflammation were observed between P-selectin/ PSGL-1 inhibitors and enoxaparin treated animals (IV95% CI; -3.59 [-10.67-3.48], p - 0.32, I(2) - 66%). In addition, there was no differences in the coagulation parameters (aPTT, TCT, BT, D-Dimer, fibrinogen, platelets) between P-selectin/ PSGL-1 inhibitors and enoxaparin (IV 95% CI; -1.12[-2.36-0.11], p = 0.07, I(2) = 92%), although there was a trend showing less of a prolongation in TCT with P-selectin/ PSGL-1 inhibitors compared to enoxaparin (p<0.0001). Conclusion: P-selectin antagonism successfully paralleled the low-molecular-weight-heparin enoxaparin, for the treatment of DVT in nonhuman primate models, by decreasing both thrombus burden and inflammation without causing any bleeding complications and without increasing coagulation times. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:E138 / E142
页数:5
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