2016
Proteomic analysis of cerebrospinal fluid for relapsing-remitting multiple sclerosis and clinically isolated syndrome
PAVELEK, Zbyšek; Oldřich VYŠATA; Vojtěch TAMBOR; Kristýna PIMKOVÁ; Dai Long VU et. al.Základní údaje
Originální název
Proteomic analysis of cerebrospinal fluid for relapsing-remitting multiple sclerosis and clinically isolated syndrome
Autoři
PAVELEK, Zbyšek; Oldřich VYŠATA; Vojtěch TAMBOR; Kristýna PIMKOVÁ; Dai Long VU; Kamil KUČA; Pavel ŠTOURAČ a Martin VALIŠ
Vydání
Biomedical Reports, Athens, Spandidos Publications, 2016, 2049-9434
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30000 3. Medical and Health Sciences
Stát vydavatele
Řecko
Utajení
není předmětem státního či obchodního tajemství
Kód RIV
RIV/00216224:14110/16:00093167
Organizační jednotka
Lékařská fakulta
UT WoS
000379957300007
EID Scopus
2-s2.0-84989848724
Klíčová slova anglicky
multiple sclerosis; clinically isolated syndrome; cerebrospinal fluid; proteomic analysis; biomarkers; proteins
Štítky
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 25. 1. 2017 12:12, Ing. Mgr. Věra Pospíšilíková
Anotace
V originále
Early diagnosis and treatment of multiple sclerosis (MS) in the initial stages of the disease can significantly retard its progression. The aim of the present study was to identify changes in the cerebrospinal fluid proteome in patients with relapsing-remitting MS and clinically isolated MS syndrome who are at high risk of developing MS (case group) compared to healthy population (control) in order to identify potential new markers, which could ultimately aid in early diagnosis of MS. The protein concentrations of each of the 11 case and 15 control samples were determined using a bicinchoninic acid assay. Nanoscale liquid chromatography coupled with tandem mass spectrometry was used for protein identification. Proteomics data were processed using the Perseus software suite and R. The results were filtered using the Benjamini-Hochberg procedure for the false discovery rate (FDR) correction (FDR<0.05). The results showed that, 26 proteins were significantly dysregulated in case samples compared to the controls. Nine proteins were found to be significantly less abundant in case samples, while the abundance of 17 proteins was significantly increased in case samples compared to controls. Three of the proteins were previously linked to RR MS, including immunoglobulin (Ig) gamma-1 chain C region, Ig heavy chain V-III region BRO and Ig kappa chain C region. Three proteins that were uniquely expressed in patients with RR MS were identified and these proteins may serve as prognostic biomarkers for identifying patients with a high risk of developing RR MS.