Cargando…

A multi‐biomarker follow‐up study of patients with multiple sclerosis

OBJECTIVES: This study aimed to examine the levels of the macrophage marker sCD163 and other biomarkers at the time of diagnosis of patients with either clinically isolated syndrome (CIS) or relapsing‐remitting multiple sclerosis (RRMS), and assess relation to clinical indicators of prognosis, disea...

Descripción completa

Detalles Bibliográficos
Autores principales: Stilund, Morten, Gjelstrup, Mikkel Carstensen, Christensen, Tove, Møller, Holger Jon, Petersen, Thor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5036432/
https://www.ncbi.nlm.nih.gov/pubmed/27688939
http://dx.doi.org/10.1002/brb3.509
_version_ 1782455554292056064
author Stilund, Morten
Gjelstrup, Mikkel Carstensen
Christensen, Tove
Møller, Holger Jon
Petersen, Thor
author_facet Stilund, Morten
Gjelstrup, Mikkel Carstensen
Christensen, Tove
Møller, Holger Jon
Petersen, Thor
author_sort Stilund, Morten
collection PubMed
description OBJECTIVES: This study aimed to examine the levels of the macrophage marker sCD163 and other biomarkers at the time of diagnosis of patients with either clinically isolated syndrome (CIS) or relapsing‐remitting multiple sclerosis (RRMS), and assess relation to clinical indicators of prognosis, disease activity (DA), and changes in the levels of these biomarkers at follow‐up. MATERIALS AND METHODS: The clinical status and MRI were reevaluated in 56 patients more than 1 year after diagnosis with a median follow‐up time of 2 years. Levels of biomarkers in serum and cerebrospinal fluid (CSF) samples were evaluated by enzyme‐linked immunosorbent assays. RESULTS: There was no significant difference in time to DA between patients with CIS and RRMS. A high sCD163 ratio (>0.07) was significantly (P = 0.04) associated with time to DA in the untreated patient group. In 21 patients reevaluated with serum and CSF samples, the sCD163 ratio levels decreased from 0.068 to 0.054 (P = 0.026) in the CIS/RRMS‐treated group. The CSF CXCL13, CXCL13 ratio, CSF neurofilament light polypeptide and osteopontin levels also decreased significantly in the CIS/RRMS‐treated group. CONCLUSIONS: The levels of all biomarkers changed concurrently with MS treatment. The sCD163 ratio was identified as a potential novel marker for time to DA.
format Online
Article
Text
id pubmed-5036432
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-50364322016-09-29 A multi‐biomarker follow‐up study of patients with multiple sclerosis Stilund, Morten Gjelstrup, Mikkel Carstensen Christensen, Tove Møller, Holger Jon Petersen, Thor Brain Behav Original Research OBJECTIVES: This study aimed to examine the levels of the macrophage marker sCD163 and other biomarkers at the time of diagnosis of patients with either clinically isolated syndrome (CIS) or relapsing‐remitting multiple sclerosis (RRMS), and assess relation to clinical indicators of prognosis, disease activity (DA), and changes in the levels of these biomarkers at follow‐up. MATERIALS AND METHODS: The clinical status and MRI were reevaluated in 56 patients more than 1 year after diagnosis with a median follow‐up time of 2 years. Levels of biomarkers in serum and cerebrospinal fluid (CSF) samples were evaluated by enzyme‐linked immunosorbent assays. RESULTS: There was no significant difference in time to DA between patients with CIS and RRMS. A high sCD163 ratio (>0.07) was significantly (P = 0.04) associated with time to DA in the untreated patient group. In 21 patients reevaluated with serum and CSF samples, the sCD163 ratio levels decreased from 0.068 to 0.054 (P = 0.026) in the CIS/RRMS‐treated group. The CSF CXCL13, CXCL13 ratio, CSF neurofilament light polypeptide and osteopontin levels also decreased significantly in the CIS/RRMS‐treated group. CONCLUSIONS: The levels of all biomarkers changed concurrently with MS treatment. The sCD163 ratio was identified as a potential novel marker for time to DA. John Wiley and Sons Inc. 2016-07-11 /pmc/articles/PMC5036432/ /pubmed/27688939 http://dx.doi.org/10.1002/brb3.509 Text en © 2016 The Authors. Brain and Behavior published by Wiley Periodicals, Inc. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Stilund, Morten
Gjelstrup, Mikkel Carstensen
Christensen, Tove
Møller, Holger Jon
Petersen, Thor
A multi‐biomarker follow‐up study of patients with multiple sclerosis
title A multi‐biomarker follow‐up study of patients with multiple sclerosis
title_full A multi‐biomarker follow‐up study of patients with multiple sclerosis
title_fullStr A multi‐biomarker follow‐up study of patients with multiple sclerosis
title_full_unstemmed A multi‐biomarker follow‐up study of patients with multiple sclerosis
title_short A multi‐biomarker follow‐up study of patients with multiple sclerosis
title_sort multi‐biomarker follow‐up study of patients with multiple sclerosis
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5036432/
https://www.ncbi.nlm.nih.gov/pubmed/27688939
http://dx.doi.org/10.1002/brb3.509
work_keys_str_mv AT stilundmorten amultibiomarkerfollowupstudyofpatientswithmultiplesclerosis
AT gjelstrupmikkelcarstensen amultibiomarkerfollowupstudyofpatientswithmultiplesclerosis
AT christensentove amultibiomarkerfollowupstudyofpatientswithmultiplesclerosis
AT møllerholgerjon amultibiomarkerfollowupstudyofpatientswithmultiplesclerosis
AT petersenthor amultibiomarkerfollowupstudyofpatientswithmultiplesclerosis
AT stilundmorten multibiomarkerfollowupstudyofpatientswithmultiplesclerosis
AT gjelstrupmikkelcarstensen multibiomarkerfollowupstudyofpatientswithmultiplesclerosis
AT christensentove multibiomarkerfollowupstudyofpatientswithmultiplesclerosis
AT møllerholgerjon multibiomarkerfollowupstudyofpatientswithmultiplesclerosis
AT petersenthor multibiomarkerfollowupstudyofpatientswithmultiplesclerosis