
@Article{ecn.2006.0048,
AUTHOR = {Arnon Blum, Khaled Khazim, Monir Merei, Aviva Peleg, Nava Blum, Vladimir Vaispapir},
TITLE = {The Stroke Trial – can we predict clinical outcome of patients with ischemic stroke by measuring soluble cell adhesion molecules (CAM)?},
JOURNAL = {European Cytokine Network},
VOLUME = {17},
YEAR = {2006},
NUMBER = {4},
PAGES = {295--298},
URL = {http://www.techscience.com/ECN/v17n4/66143},
ISSN = {1952-4005},
ABSTRACT = {Background. Several studies have found that an increased concentration of haemostatic or
inﬂammation markers was associated with worse prognosis in vascular disease. The inﬂammatory components in
ischemic stroke are of current interest, and there is some experimental evidence that they may be linked.
Hypothesis. The study was performed to determine the association between the neurological clinical outcome and
levels of cell adhesion molecules in the ﬁrst four days of hospitalization in patients with acute ischemic event.
Methods. This prospective, pilot, case-controlled study examined the association between the clinical outcome and
inﬂammatory markers within the ﬁrst few days of hospitalization. The neurological evaluation was performed
using the NIH score on admission and four days later, and levels of cell adhesion molecules were measured by
ELISA methods on admission and four days later. Results. Twenty three patients with an acute cerebral event
(mean age 71 ± 15 y, 12 women and 11 men) were examined neurologically on admission and four days later.
Among 19 patients who improved, there was a signiﬁcant decrease in the NIH neurological scale, from 3.8 ± 3.2
to 1.3 ± 1.8 (p = 0.01), which was accompanied by a signiﬁcant decrease in the cell adhesion molecules that were
measured (E-selectin, ICAM-1 and VCAM-1). Of the four patients who did not improve, their mean clinical NIH
score was 10 ± 4.6 and worsened or remained unchanged after four days of follow-up. In this group, we could not
demonstrate a signiﬁcant change in levels of cell adhesion molecules between days one and four. Conclusions.
Patients who improved clinically within the ﬁrst four days of hospitalization demonstrated a remarkable
inhibition of all three cell adhesion molecules that were measured (E-selectin, ICAM-1, and VCAM-1). Patients
who did not improve had more severe cerebral infarcts, a higher NIH score on admission (10 ± 4.6), and no change
was observed in levels of cell adhesion molecules during the follow-up period. Measuring cell adhesion molecule
levels may predict objectively the clinical outcome in hospitalized patients with acute ischemic stroke.},
DOI = {10.1684/ecn.2006.0048}
}



