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Differences between blood and cerebrospinal fluid glial fibrillary Acidic protein levels: The effect of sample stability
INTRODUCTION: Recent evidence has shown that the marker of reactive astrogliosis, glial fibrillary acidic protein (GFAP), has a stronger relationship with cerebral amyloid beta (Aβ) pathology in blood than in cerebrospinal fluid (CSF). This study investigates if pre‐analytical treatment of blood and...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9826213/ https://www.ncbi.nlm.nih.gov/pubmed/36102852 http://dx.doi.org/10.1002/alz.12806 |
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author | Simrén, Joel Weninger, Haley Brum, Wagner S. Khalil, Shilla Benedet, Andréa L. Blennow, Kaj Zetterberg, Henrik Ashton, Nicholas J. |
author_facet | Simrén, Joel Weninger, Haley Brum, Wagner S. Khalil, Shilla Benedet, Andréa L. Blennow, Kaj Zetterberg, Henrik Ashton, Nicholas J. |
author_sort | Simrén, Joel |
collection | PubMed |
description | INTRODUCTION: Recent evidence has shown that the marker of reactive astrogliosis, glial fibrillary acidic protein (GFAP), has a stronger relationship with cerebral amyloid beta (Aβ) pathology in blood than in cerebrospinal fluid (CSF). This study investigates if pre‐analytical treatment of blood and CSF contribute to these unexpected findings. METHODS: Paired CSF and serum samples from 49 individuals (Aβ‐negative = 28; Aβ‐positive = 21) underwent a series of seven freeze‐thaw cycles (FTCs). All samples were analyzed for GFAP and neurofilament light (NfL) using single molecule array technology including a fresh unfrozen sample from each patient. RESULTS: FTC significantly affected CSF GFAP concentration (−188.12 pg/ml per FTC) but not serum GFAP. In the same samples, NfL remained stable. Serum GFAP had a higher discrimination of Aβ burden than CSF GFAP, irrespective of FTC, which also included unfrozen samples. DISCUSSION: This study demonstrates large stability differences of GFAP in CSF and serum. However, this disparity does not seem to fully explain the stronger association of serum GFAP with Aβ pathology. Further work should investigate mechanisms of GFAP release into the bloodstream under pathological conditions. |
format | Online Article Text |
id | pubmed-9826213 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98262132023-01-09 Differences between blood and cerebrospinal fluid glial fibrillary Acidic protein levels: The effect of sample stability Simrén, Joel Weninger, Haley Brum, Wagner S. Khalil, Shilla Benedet, Andréa L. Blennow, Kaj Zetterberg, Henrik Ashton, Nicholas J. Alzheimers Dement Short Report INTRODUCTION: Recent evidence has shown that the marker of reactive astrogliosis, glial fibrillary acidic protein (GFAP), has a stronger relationship with cerebral amyloid beta (Aβ) pathology in blood than in cerebrospinal fluid (CSF). This study investigates if pre‐analytical treatment of blood and CSF contribute to these unexpected findings. METHODS: Paired CSF and serum samples from 49 individuals (Aβ‐negative = 28; Aβ‐positive = 21) underwent a series of seven freeze‐thaw cycles (FTCs). All samples were analyzed for GFAP and neurofilament light (NfL) using single molecule array technology including a fresh unfrozen sample from each patient. RESULTS: FTC significantly affected CSF GFAP concentration (−188.12 pg/ml per FTC) but not serum GFAP. In the same samples, NfL remained stable. Serum GFAP had a higher discrimination of Aβ burden than CSF GFAP, irrespective of FTC, which also included unfrozen samples. DISCUSSION: This study demonstrates large stability differences of GFAP in CSF and serum. However, this disparity does not seem to fully explain the stronger association of serum GFAP with Aβ pathology. Further work should investigate mechanisms of GFAP release into the bloodstream under pathological conditions. John Wiley and Sons Inc. 2022-09-14 2022-10 /pmc/articles/PMC9826213/ /pubmed/36102852 http://dx.doi.org/10.1002/alz.12806 Text en © 2022 The Authors. Alzheimer's & Dementia published by Wiley Periodicals LLC on behalf of Alzheimer's Association. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Short Report Simrén, Joel Weninger, Haley Brum, Wagner S. Khalil, Shilla Benedet, Andréa L. Blennow, Kaj Zetterberg, Henrik Ashton, Nicholas J. Differences between blood and cerebrospinal fluid glial fibrillary Acidic protein levels: The effect of sample stability |
title | Differences between blood and cerebrospinal fluid glial fibrillary Acidic protein levels: The effect of sample stability |
title_full | Differences between blood and cerebrospinal fluid glial fibrillary Acidic protein levels: The effect of sample stability |
title_fullStr | Differences between blood and cerebrospinal fluid glial fibrillary Acidic protein levels: The effect of sample stability |
title_full_unstemmed | Differences between blood and cerebrospinal fluid glial fibrillary Acidic protein levels: The effect of sample stability |
title_short | Differences between blood and cerebrospinal fluid glial fibrillary Acidic protein levels: The effect of sample stability |
title_sort | differences between blood and cerebrospinal fluid glial fibrillary acidic protein levels: the effect of sample stability |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9826213/ https://www.ncbi.nlm.nih.gov/pubmed/36102852 http://dx.doi.org/10.1002/alz.12806 |
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