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...
Autores principales: | , , , , |
---|---|
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 |