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

Eduardo Ramacciotti, Daniel D Myers Jr, Shirley K Wrobleski, K Barry Deatrick, Frank J Londy, John E Rectenwald, Peter K Henke, Robert G Schaub, Thomas W Wakefield, Eduardo Ramacciotti, Daniel D Myers Jr, Shirley K Wrobleski, K Barry Deatrick, Frank J Londy, John E Rectenwald, Peter K Henke, Robert G Schaub, Thomas W Wakefield

Abstract

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.

Figures

Figure 1
Figure 1
Forest plot of comparison: P-selectin inhibitors vs. saline, outcome: vein re-opening. Note that the mean difference in inverse variance was 44.37 in favor of P-selectin inhibitors.
Figure 2
Figure 2
Forest plot of comparison: P-selectin inhibitors vs. enoxaparin, outcome: Vein re-opening
Figure 3
Figure 3
Forest plot of comparison: P-selectin inhibitors vs. saline, outcome: Gd Enhancement (Inflammation)
Figure 4
Figure 4
Forest plot of comparison: P-selectin inhibitors vs. enoxaparin, outcome: Gd Enhancement (Inflammation)
Figure 5
Figure 5
Forest plot of comparison: P-selectin inhibitor vs. enoxaparin, outcome: coagulation tests 6 days post thrombosis.

Source: PubMed

3
Abonnieren