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Article type: Research Article
Authors: Selakovic, Vesna | Raicevic, Ranko | Radenovic, Lidija
Affiliations: Institute for Medical Research, MMA, Belgrade, Serbia | Clinic of Neurology, MMA, Belgrade, Serbia | Department of Physiology and Biochemistry, Faculty of Biology, University of Belgrade, Serbia
Note: [] Corresponding author: Lidija Radenovic, Ph.D. Associate Professor, Department of Physiology and Biochemistry, Faculty of Biology, University of Belgrade, P.O.B. 52, Studentski trg 16, 11000 Belgrade, Serbia. Tel.: +381 11 3032356; Fax: +381 11 2638500; 3032356; E-mail: [email protected]
Abstract: The aim of this study was to define concentration changes of soluble adhesion molecules (sICAM-1, sVCAM-1 and sE-Selectin) in cerebrospinal fluid and plasma, as well as, number of peripheral blood leukocytes and the albumin coefficient in the patients with the acute brain infarction. We also, analyzed the correlation between the measured levels, the infarct volume and the degree of neurological and the functional deficit. The study included 50 patients with the acute cerebral infarction and the control group consisted of 16 patients, age and sex matched. Obtained results showed significant increase in number of leukocytes, the albumin coefficient and the level of soluble adhesion molecules within the first seven days in patients. The highest values of measured parameters were noted within the third and the fourth day after the insult, which is the suggested period of maximal intensity of inflammatory reactions. Significant correlation was found between measured parameters and the infarct volume, the degree of neurological and the functional deficit. The results suggest that investigated parameters in CSF and blood represent a dynamic index of inflammatory events as one of the fundametal mechanisms responsible for neuron damage during acute phase of brain infarction.
Keywords: Brain infarction, inflammation, soluble adhesion molecules, leukocytes number, albumin coefficient, cerebrospinal fluid
DOI: 10.3233/DMA-2009-0608
Journal: Disease Markers, vol. 26, no. 2, pp. 65-74, 2009
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