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Cerebrospinal fluid metallomics in cerebral amyloid angiopathy: an exploratory analysis

INTRODUCTION: Cerebral amyloid angiopathy (CAA) is associated with symptomatic intracerebral haemorrhage. Biomarkers of clinically silent bleeding events, such as cerebrospinal fluid (CSF) ferritin and iron, might provide novel measures of disease presence and severity. METHODS: We performed an expl...

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Autores principales: Banerjee, Gargi, Forsgard, Niklas, Ambler, Gareth, Keshavan, Ashvini, Paterson, Ross W., Foiani, Martha S., Toombs, Jamie, Heslegrave, Amanda, Thompson, Edward J., Lunn, Michael P., Fox, Nick C., Zetterberg, Henrik, Schott, Jonathan M., Werring, David J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8857160/
https://www.ncbi.nlm.nih.gov/pubmed/34292397
http://dx.doi.org/10.1007/s00415-021-10711-6
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author Banerjee, Gargi
Forsgard, Niklas
Ambler, Gareth
Keshavan, Ashvini
Paterson, Ross W.
Foiani, Martha S.
Toombs, Jamie
Heslegrave, Amanda
Thompson, Edward J.
Lunn, Michael P.
Fox, Nick C.
Zetterberg, Henrik
Schott, Jonathan M.
Werring, David J.
author_facet Banerjee, Gargi
Forsgard, Niklas
Ambler, Gareth
Keshavan, Ashvini
Paterson, Ross W.
Foiani, Martha S.
Toombs, Jamie
Heslegrave, Amanda
Thompson, Edward J.
Lunn, Michael P.
Fox, Nick C.
Zetterberg, Henrik
Schott, Jonathan M.
Werring, David J.
author_sort Banerjee, Gargi
collection PubMed
description INTRODUCTION: Cerebral amyloid angiopathy (CAA) is associated with symptomatic intracerebral haemorrhage. Biomarkers of clinically silent bleeding events, such as cerebrospinal fluid (CSF) ferritin and iron, might provide novel measures of disease presence and severity. METHODS: We performed an exploratory study comparing CSF iron, ferritin, and other metal levels in patients with CAA, control subjects (CS) and patients with Alzheimer’s disease (AD). Ferritin was measured using a latex fixation test; metal analyses were performed using inductively coupled plasma mass spectrometry. RESULTS: CAA patients (n = 10) had higher levels of CSF iron than the AD (n = 20) and CS (n = 10) groups (medians 23.42, 15.48 and 17.71 μg/L, respectively, p = 0.0015); the difference between CAA and AD groups was significant in unadjusted and age-adjusted analyses. We observed a difference in CSF ferritin (medians 10.10, 7.77 and 8.01 ng/ml, for CAA, AD and CS groups, respectively, p = 0.01); the difference between the CAA and AD groups was significant in unadjusted, but not age-adjusted, analyses. We also observed differences between the CAA and AD groups in CSF nickel and cobalt (unadjusted analyses). CONCLUSIONS: In this exploratory study, we provide preliminary evidence for a distinct CSF metallomic profile in patients with CAA. Replication and validation of these results in larger cohorts is needed. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00415-021-10711-6.
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spelling pubmed-88571602022-02-23 Cerebrospinal fluid metallomics in cerebral amyloid angiopathy: an exploratory analysis Banerjee, Gargi Forsgard, Niklas Ambler, Gareth Keshavan, Ashvini Paterson, Ross W. Foiani, Martha S. Toombs, Jamie Heslegrave, Amanda Thompson, Edward J. Lunn, Michael P. Fox, Nick C. Zetterberg, Henrik Schott, Jonathan M. Werring, David J. J Neurol Original Communication INTRODUCTION: Cerebral amyloid angiopathy (CAA) is associated with symptomatic intracerebral haemorrhage. Biomarkers of clinically silent bleeding events, such as cerebrospinal fluid (CSF) ferritin and iron, might provide novel measures of disease presence and severity. METHODS: We performed an exploratory study comparing CSF iron, ferritin, and other metal levels in patients with CAA, control subjects (CS) and patients with Alzheimer’s disease (AD). Ferritin was measured using a latex fixation test; metal analyses were performed using inductively coupled plasma mass spectrometry. RESULTS: CAA patients (n = 10) had higher levels of CSF iron than the AD (n = 20) and CS (n = 10) groups (medians 23.42, 15.48 and 17.71 μg/L, respectively, p = 0.0015); the difference between CAA and AD groups was significant in unadjusted and age-adjusted analyses. We observed a difference in CSF ferritin (medians 10.10, 7.77 and 8.01 ng/ml, for CAA, AD and CS groups, respectively, p = 0.01); the difference between the CAA and AD groups was significant in unadjusted, but not age-adjusted, analyses. We also observed differences between the CAA and AD groups in CSF nickel and cobalt (unadjusted analyses). CONCLUSIONS: In this exploratory study, we provide preliminary evidence for a distinct CSF metallomic profile in patients with CAA. Replication and validation of these results in larger cohorts is needed. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00415-021-10711-6. Springer Berlin Heidelberg 2021-07-22 2022 /pmc/articles/PMC8857160/ /pubmed/34292397 http://dx.doi.org/10.1007/s00415-021-10711-6 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Communication
Banerjee, Gargi
Forsgard, Niklas
Ambler, Gareth
Keshavan, Ashvini
Paterson, Ross W.
Foiani, Martha S.
Toombs, Jamie
Heslegrave, Amanda
Thompson, Edward J.
Lunn, Michael P.
Fox, Nick C.
Zetterberg, Henrik
Schott, Jonathan M.
Werring, David J.
Cerebrospinal fluid metallomics in cerebral amyloid angiopathy: an exploratory analysis
title Cerebrospinal fluid metallomics in cerebral amyloid angiopathy: an exploratory analysis
title_full Cerebrospinal fluid metallomics in cerebral amyloid angiopathy: an exploratory analysis
title_fullStr Cerebrospinal fluid metallomics in cerebral amyloid angiopathy: an exploratory analysis
title_full_unstemmed Cerebrospinal fluid metallomics in cerebral amyloid angiopathy: an exploratory analysis
title_short Cerebrospinal fluid metallomics in cerebral amyloid angiopathy: an exploratory analysis
title_sort cerebrospinal fluid metallomics in cerebral amyloid angiopathy: an exploratory analysis
topic Original Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8857160/
https://www.ncbi.nlm.nih.gov/pubmed/34292397
http://dx.doi.org/10.1007/s00415-021-10711-6
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