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Increased Levels of Chitotriosidase and YKL-40 in Cerebrospinal Fluid from Patients with Alzheimer's Disease
BACKGROUND: The cerebrospinal fluid (CSF) biomarkers total tau, abnormally phosphorylated tau and amyloid β 1-42 are strongly associated with Alzheimer's disease (AD). Apart from the pathologic hallmarks that these biomarkers represent, other processes such as inflammation and microglial activa...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
S. Karger AG
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4164083/ https://www.ncbi.nlm.nih.gov/pubmed/25254036 http://dx.doi.org/10.1159/000362164 |
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author | Rosén, Christoffer Andersson, Carl-Henrik Andreasson, Ulf Molinuevo, José L. Bjerke, Maria Rami, Lorena Lladó, Albert Blennow, Kaj Zetterberg, Henrik |
author_facet | Rosén, Christoffer Andersson, Carl-Henrik Andreasson, Ulf Molinuevo, José L. Bjerke, Maria Rami, Lorena Lladó, Albert Blennow, Kaj Zetterberg, Henrik |
author_sort | Rosén, Christoffer |
collection | PubMed |
description | BACKGROUND: The cerebrospinal fluid (CSF) biomarkers total tau, abnormally phosphorylated tau and amyloid β 1-42 are strongly associated with Alzheimer's disease (AD). Apart from the pathologic hallmarks that these biomarkers represent, other processes such as inflammation and microglial activation are present in the brains of patients with AD. New biomarkers related to these processes could be valuable for the diagnosis and follow-up of AD patients and for the evaluation of inflammation-related pathologies. AIM: The aim of this study was to evaluate the association of inflammatory CSF biomarkers with AD. METHODS: Twenty-five AD patients and 25 controls who had a pathological and normal CSF profile of the core AD biomarkers, respectively, were included in this study. CSF levels of chitotriosidase, YKL-40 (also known as chitinase-3-like protein 1) and monocyte chemoattractant protein-1 (MCP-1) were quantified and the levels compared between the groups. RESULTS: AD patients had increased CSF levels of chitotriosidase and YKL-40 (both approximately twice higher than in controls), while the levels of MCP-1 were similar in the AD and control groups. CONCLUSION: The results indicate that chitotriosidase and YKL-40 may be helpful for the evaluation of cerebral inflammatory activity in AD patients. |
format | Online Article Text |
id | pubmed-4164083 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | S. Karger AG |
record_format | MEDLINE/PubMed |
spelling | pubmed-41640832014-09-24 Increased Levels of Chitotriosidase and YKL-40 in Cerebrospinal Fluid from Patients with Alzheimer's Disease Rosén, Christoffer Andersson, Carl-Henrik Andreasson, Ulf Molinuevo, José L. Bjerke, Maria Rami, Lorena Lladó, Albert Blennow, Kaj Zetterberg, Henrik Dement Geriatr Cogn Dis Extra Original Research Article BACKGROUND: The cerebrospinal fluid (CSF) biomarkers total tau, abnormally phosphorylated tau and amyloid β 1-42 are strongly associated with Alzheimer's disease (AD). Apart from the pathologic hallmarks that these biomarkers represent, other processes such as inflammation and microglial activation are present in the brains of patients with AD. New biomarkers related to these processes could be valuable for the diagnosis and follow-up of AD patients and for the evaluation of inflammation-related pathologies. AIM: The aim of this study was to evaluate the association of inflammatory CSF biomarkers with AD. METHODS: Twenty-five AD patients and 25 controls who had a pathological and normal CSF profile of the core AD biomarkers, respectively, were included in this study. CSF levels of chitotriosidase, YKL-40 (also known as chitinase-3-like protein 1) and monocyte chemoattractant protein-1 (MCP-1) were quantified and the levels compared between the groups. RESULTS: AD patients had increased CSF levels of chitotriosidase and YKL-40 (both approximately twice higher than in controls), while the levels of MCP-1 were similar in the AD and control groups. CONCLUSION: The results indicate that chitotriosidase and YKL-40 may be helpful for the evaluation of cerebral inflammatory activity in AD patients. S. Karger AG 2014-07-31 /pmc/articles/PMC4164083/ /pubmed/25254036 http://dx.doi.org/10.1159/000362164 Text en Copyright © 2014 by S. Karger AG, Basel http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article licensed under the terms of the Creative Commons Attribution-NonCommercial 3.0 Unported license (CC BY-NC) (www.karger.com/OA-license), applicable to the online version of the article only. Users may download, print and share this work on the Internet for noncommercial purposes only, provided the original work is properly cited, and a link to the original work on http://www.karger.com and the terms of this license are included in any shared versions. |
spellingShingle | Original Research Article Rosén, Christoffer Andersson, Carl-Henrik Andreasson, Ulf Molinuevo, José L. Bjerke, Maria Rami, Lorena Lladó, Albert Blennow, Kaj Zetterberg, Henrik Increased Levels of Chitotriosidase and YKL-40 in Cerebrospinal Fluid from Patients with Alzheimer's Disease |
title | Increased Levels of Chitotriosidase and YKL-40 in Cerebrospinal Fluid from Patients with Alzheimer's Disease |
title_full | Increased Levels of Chitotriosidase and YKL-40 in Cerebrospinal Fluid from Patients with Alzheimer's Disease |
title_fullStr | Increased Levels of Chitotriosidase and YKL-40 in Cerebrospinal Fluid from Patients with Alzheimer's Disease |
title_full_unstemmed | Increased Levels of Chitotriosidase and YKL-40 in Cerebrospinal Fluid from Patients with Alzheimer's Disease |
title_short | Increased Levels of Chitotriosidase and YKL-40 in Cerebrospinal Fluid from Patients with Alzheimer's Disease |
title_sort | increased levels of chitotriosidase and ykl-40 in cerebrospinal fluid from patients with alzheimer's disease |
topic | Original Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4164083/ https://www.ncbi.nlm.nih.gov/pubmed/25254036 http://dx.doi.org/10.1159/000362164 |
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