Cerebrospinal fluid proteome comparison between multiple sclerosis patients and controls

被引:62
|
作者
Kroksveen, A. C. [1 ,2 ]
Guldbrandsen, A. [1 ,2 ]
Vedeler, C. [1 ,3 ]
Myhr, K. M. [1 ,3 ]
Opsahl, J. A. [2 ]
Berven, F. S. [1 ,2 ,3 ]
机构
[1] Univ Bergen, Dept Clin Med, KG Jebsen Ctr MS Res, Bergen, Norway
[2] Univ Bergen, Dept Biomed, Prote Unit PROBE, Bergen, Norway
[3] Haukeland Hosp, Dept Neurol, Norwegian Multiple Sclerosis Competence Ctr, N-5021 Bergen, Norway
来源
关键词
multiple sclerosis; cerebrospinal fluid; biomarkers; proteomics; label-free quantitative mass spectrometry; IgG; vitamin D-binding protein; D-BINDING PROTEIN; APOLIPOPROTEIN-D EXPRESSION; CENTRAL-NERVOUS-SYSTEM; VITAMIN-D; OLIGODENDROCYTE MATURATION; DIAGNOSTIC-CRITERIA; GC-GLOBULIN; PLASMA; CONVERSION; RECEPTOR;
D O I
10.1111/ane.12029
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objectives - The aim of the present study was to identify proteins in cerebrospinal fluid (CSF) with different abundance between patients with relapsing-remitting multiple sclerosis (RRMS) and controls. Such proteins may be diagnostic biomarkers and contribute with novel information about the disease pathogenesis. Materials and methods - Cerebrospinal fluid from patients with RRMS (n = 17) and controls (n = 17) were trypsin digested and analyzed in a label-free fashion using liquid chromatography mass spectrometry. The resulting data were analyzed using SearchGUI, PeptideShaker, and the Progenesis software. Results - Two hundred and ninety-one proteins were identified, of which 32 were significantly differentially abundant between the patients with RRMS and controls (P-value <= 0.05, two or more peptides quantified). Among these were proteins which previously have been linked to MS, including immunoglobulin subunits, vitamin D-binding protein, apolipoprotein D, kallikrein-6, neuronal pentraxin receptor, Dickkopf-related protein 3, and contactin-1. Conclusion - The study provides an overview of differentially abundant proteins between RRMS and controls, and a few of these are further discussed. It should be stressed that a larger verification study is needed to reveal the potential value of these proteins as biomarkers for RRMS and their involvement in the disease pathogenesis.
引用
收藏
页码:90 / 96
页数:7
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