Pregled bibliografske jedinice broj: 88207
Cerebrospinal fluid and serum Interleukin-6 and its receptors levels in relapsing-remitting multiple sclerosis patients
Cerebrospinal fluid and serum Interleukin-6 and its receptors levels in relapsing-remitting multiple sclerosis patients // European Journal of Neurology
Oxford: Wiley-Blackwell, 2002. str. 135-135 (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 88207 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Cerebrospinal fluid and serum Interleukin-6 and its receptors levels in relapsing-remitting multiple sclerosis patients
Autori
Horvat, Gordana ; Vladić, Anton ; Zadro, Ivana ; Vukadin, Stipe ; Čulo, Filip
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
European Journal of Neurology
/ - Oxford : Wiley-Blackwell, 2002, 135-135
Skup
6th Congress of European Federation of Neurological Societies
Mjesto i datum
Beč, Austrija, 26.10.2002. - 29.10.2002
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
Il-6; RRMS; CSF; serum
Sažetak
Introduction: Inteleukin-6 (IL-6) has recently been implicated in the pathogenesis of multiple sclerosis, as it was found localized in MS lesions. The functional receptor for IL-6 is a complex of signal transducing subunit glycoprotein 130 (sgp130) and the ligand binding subunit gp80 (sIL-6R). They interact to mediate intracellular signalling. The aim of this study was to measure IL-6 and its soluble receptors (sIL-6R and sgp130) in the cerebrospinal fluid (CSF) and serum from relapsing-remitting MS patients (RRMS). Patients and methods: We analysed CSF and serum samples of 21 RRMS patients during acute exacerbation of the disease, and 19 patients with noninflammatory neurological diseases (NIND), as controls. IL-6, sIL-6R and sgp130 levels were measured using enzymeimmuno test (ELISA). One-way ANOVA was applied for statistical analysis of the data. Results: Our preliminary results (mean&plusmn ; S.D. in pg/mL) showed statistically different serum IL-6 level in RRMS (27.79&plusmn ; 61.33) and NIND (106.04&plusmn ; 125.93) patients. However, there was no statistical difference between CSF IL-6 level in RRMS (2.90&plusmn ; 2.68) and NIND (2.97&plusmn ; 2.59) patients. Serum sIL-6R level was not statistically different between RRMS (25 795.55&plusmn ; 8511.27) and NIND (21840.12&plusmn ; 6379.43) patients, but CSF level were statistically different between RRMS (630.26&plusmn ; 522.19) and NIND (159.84&plusmn ; 273.41) group. Serum sgp130 levels were statistically different in RRMS (333750&plusmn ; 88070) and NIND (415590&plusmn ; 124160) patients. The CSF sgp130 level between RRMS (46710&plusmn ; 26280) and NIND (54250&plusmn ; 22560) group was not statistically different. Conclusion: Our preliminary results suggest that IL-6 and its soluble receptors (sIL-6R and sgp130) regulation may be altered in RRMS during acute exacerbation of the disease.
Izvorni jezik
Engleski
Znanstvena područja
Farmacija
POVEZANOST RADA
Ustanove:
Medicinski fakultet, Zagreb