Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2934300 | International Journal of Cardiology | 2009 | 5 Pages |
BackgroundThere is increasing evidence that cellular adhesion molecules (CAMs) play an important role in the pathophysiology of acute ischaemic stroke. We examined the prognostic value of soluble intercellular adhesion molecule-1 (sICAM-1) and soluble vascular cell adhesion molecule-1 (sVCAM-1) on in-hospital mortality in patients with ischaemic stroke.MethodsWe recruited 241 consecutive patients ≤ 65 years of age who were admitted with acute ischaemic stroke. Serum levels of sICAM-1 and sVCAM-1 were determined within 12 h from admission. Seventy-six subjects without evidence of cardiovascular disease, matched for age and sex, served as controls.ResultsPatients with acute ischaemic stroke had higher sICAM levels compared to controls [267 (220–325) versus 200 (179–225) ng/ml, p < 0.001]. Sixteen (6.6%) patients died during hospitalization. sICAM-1 and sVCAM-1 levels were significantly higher in patients who died compared to those who survived [370 (324–453) versus 260 (219–313) ng/ml, p < 0.001 and 790 (495–985) versus 576 (494–671) ng/ml, p = 0.01, respectively] but only sICAM-1 levels were independently associated with early death, after adjusting for various confounding factors. For 10 ng/ml increase in sICAM-1 levels there was a 9% higher risk of dying. Cut-off point analysis revealed that sICAM-1 levels > 322 ng/ml were the optimal points that discriminated those who died from the rest of the patients.ConclusionsHigh sICAM-1 levels on admission are associated with early death in ischaemic middle-aged stroke patients suggesting a pathogenetic role of inflammation in the evolution of ischaemic stroke.