Pregled bibliografske jedinice broj: 1228362
Clinical relevance of antibodies against myelin oligodendrocyte glycoprotein in different clinical types of multiple sclerosis
Clinical relevance of antibodies against myelin oligodendrocyte glycoprotein in different clinical types of multiple sclerosis // Clinical Neurology and Neurosurgery, 109 (2007), 1; 23-26 doi:10.1016/j.clineuro.2006.04.006 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 1228362 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Clinical relevance of antibodies against myelin
oligodendrocyte glycoprotein in different clinical
types of multiple sclerosis
Autori
Zadro, Ivana ; Brinar, Vesna ; Horvat, Gordana ; Brinar, Marko
Izvornik
Clinical Neurology and Neurosurgery (0303-8467) 109
(2007), 1;
23-26
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
myelin oligodendrocyte glycoprotein ; multiple sclerosis ; clinical type
Sažetak
Objective: Myelin oligodendrocyte glycoprotein (MOG) is a highly immunogenic minor component on the outside surface of CNS myelin which is believed to be one of the autoantigens in multiple sclerosis. The aim of this study was to evaluate the diagnostic potential of anti-MOG IgG antibody levels in cerebrospinal fluid (CSF) and serum of patients with relapsing-remitting multiple sclerosis (RRMS), primary progressive multiple sclerosis (PPMS) and non-inflammatory neurological diseases (NIND) as markers for the different clinical types of multiple sclerosis. Patients and methods: Consecutive serum and cerebrospinal fluid samples were taken from 21 patients with RRMS, 7 patients with PPMS and 19 patients with NIND. The antibody responses to MOG were determined in paired samples of these different clinical groups by enzyme-linked immunoassay using a recombinant human MOG protein. Results: The performed analysis indicated that the differences in levels of anti-MOG IgG antibody in serum and cerebrospinal fluid from the patients with RRMS, PPMS or NIND were not statistically significant. Conclusion: The assay is not sensitive or specific enough to be used as a differential diagnostic tool for the clinical types of MS, nor for MS itself.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
POVEZANOST RADA
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE