Decreased Neuro-Axonal Proteins in CSF at First Attack of Suspected Multiple Sclerosis.
Marcel P StoopTessel F RuniaChristoph StinglRoos M van der Vuurst de VriesTheo M LuiderRogier Q HintzenPublished in: Proteomics. Clinical applications (2017)
The pathology of multiple sclerosis is located in the central nervous system, therefore cerebrospinal fluid (CSF) is an attractive biofluid for biomarker research for proteins related to the early stages of this disease. In this study, the CSF proteome of patients with a clinically isolated syndrome of demyelination (CIS, a first attack of multiple sclerosis) is compared to the CSF proteome of control patients to identify differentially abundant proteins. CSF samples of 47 CIS patients and 45 control subjects are enzymatically digested and subsequently measured by LC-MS/MS (LTQ-Orbitrap). Following mass spectrometry differential abundances of the identified proteins between groups are investigated. A total of 3159 peptides are identified, relating to 485 proteins. One protein is significantly more abundant in CSF of CIS patients than in controls: Ig kappa chain C region. In contrast, 35 proteins are significantly lower in CIS patients than controls, most of them with functions in nervous system development and function, such as amyloid-like protein 1 (validated by ELISA in an independent sample set (p < 0.01)), contactin 1, contactin 2 and neuronal cell adhesion molecule. A remarkably lower abundance of neuro-axonal proteins is observed in patients with a first demyelinating event compared to controls.
Keyphrases
- multiple sclerosis
- end stage renal disease
- mass spectrometry
- ejection fraction
- chronic kidney disease
- cerebrospinal fluid
- prognostic factors
- magnetic resonance imaging
- spinal cord injury
- patient reported outcomes
- immune response
- magnetic resonance
- high resolution
- inflammatory response
- risk assessment
- microbial community
- blood brain barrier
- protein protein