Key result
Embolic events in infective endocarditis are linked to ~2-fold higher plasma P-selectin levels.
Why the study?
Inflammation-induced procoagulant changes and endothelial cell activation appear to play an important role in thromboembolic complications of infective endocarditis, motivating a comparison of plasma soluble E- and P-selectin levels across patients with and without embolic events and healthy subjects.
Are plasma levels of soluble adhesion molecules E-selectin and P-selectin elevated in infective endocarditis patients with embolic events compared to those without embolic events and healthy controls?
Observational (n=76)
Are plasma levels of soluble adhesion molecules E-selectin and P-selectin elevated in infective endocarditis patients with embolic events compared to those without embolic events and healthy controls?
Absolute Event Rate: 58.69% vs 29.65%
p-value: p=<0.001
Elevated plasma levels of soluble E-selectin and P-selectin are associated with embolic events in patients with infective endocarditis and may serve as useful markers to identify patients at high thromboembolic risk.
Higher selectin levels may flag embolic risk in infective endocarditis; hypothesis-generating and should not change practice.
AIMS: Inflammation-induced procoagulant changes and endothelial cell activation appear to play an important role in thromboembolic complications of infective endocarditis. Hence, the aim of this study was to compare the plasma levels of soluble adhesion molecules E- and P-selectin in infective endocarditis patients with and without embolic events, and healthy subjects. METHODS AND RESULTS: The study group consisted of 76 consecutive patients (mean age=26 years old, range from 8 to 64 years) with definite infective endocarditis according to the Duke criteria. Thirteen of the patients (17.1%) had embolic events. Transoesophageal echocardiographic examinations were performed on all patients within 3 days of initiation of antimicrobial therapy. Although there was a trend towards a higher rate of vegetations detected in those with embolic events than in those without, this did not reach statistical significance (84.6% vs 80.9%, P>0.05). Significantly larger vegetations were observed in patients with embolic events as compared to those without embolic events (1.4 cm vs 1.0 cm, P=0.03). The mean plasma concentrations of P-selectin were elevated in patients with embolic events as compared to both patients without embolic events and control subjects (58.69+/-7.49 ng x ml(-1)vs 29.65+/-5.69 ng x ml(-1), P=<0.001 and 58.69+/- 7.49 ng x ml(-1) vs 25.82+/-5.38 ng x ml(-1), P<0.001). Similarly, the patients with embolic events had increased plasma levels of E-selectin compared to those without embolic events and the control group (73.15+/-11.47 ng x ml(-1) vs 42.84+/-8.77 ng x ml(-1), P<0.001 and 73.15+/- 11.47 ng x ml(-1) vs 34.23+/-5.92 ng x ml(-1), P<0.001). CONCLUSION: Determination of these membrane activation molecules may provide useful markers with which to identify patients at high thromboembolic risk from infective endocarditis.
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Şule Korkmaz (2001) conducted an observational in Infective endocarditis (n=76). Embolic events in infective endocarditis vs. Infective endocarditis patients without embolic events and healthy subjects was evaluated on Plasma levels of soluble adhesion molecules P-selectin and E-selectin (ng/mL) (p=<0.001). Embolic events in infective endocarditis were associated with higher plasma P-selectin (58.69 vs 29.65 ng/mL, P<0.001) and E-selectin (73.15 vs 42.84 ng/mL, P<0.001) than non-embolic cases.
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