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Distinct Cerebrospinal Fluid Lipid Signature in Patients with Subarachnoid Hemorrhage-Induced Hydrocephalus

Patients with subarachnoid hemorrhage (SAH) may develop posthemorrhagic hydrocephalus (PHH), which is treated with surgical cerebrospinal fluid (CSF) diversion. This diversion is associated with risk of infection and shunt failure. Biomarkers for PHH etiology, CSF dynamics disturbances, and potentia...

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Autores principales: Toft-Bertelsen, Trine L., Andreassen, Søren Norge, Rostgaard, Nina, Olsen, Markus Harboe, Norager, Nicolas H., Capion, Tenna, Juhler, Marianne, MacAulay, Nanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10525923/
https://www.ncbi.nlm.nih.gov/pubmed/37760800
http://dx.doi.org/10.3390/biomedicines11092360
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author Toft-Bertelsen, Trine L.
Andreassen, Søren Norge
Rostgaard, Nina
Olsen, Markus Harboe
Norager, Nicolas H.
Capion, Tenna
Juhler, Marianne
MacAulay, Nanna
author_facet Toft-Bertelsen, Trine L.
Andreassen, Søren Norge
Rostgaard, Nina
Olsen, Markus Harboe
Norager, Nicolas H.
Capion, Tenna
Juhler, Marianne
MacAulay, Nanna
author_sort Toft-Bertelsen, Trine L.
collection PubMed
description Patients with subarachnoid hemorrhage (SAH) may develop posthemorrhagic hydrocephalus (PHH), which is treated with surgical cerebrospinal fluid (CSF) diversion. This diversion is associated with risk of infection and shunt failure. Biomarkers for PHH etiology, CSF dynamics disturbances, and potentially subsequent shunt dependency are therefore in demand. With the recent demonstration of lipid-mediated CSF hypersecretion contributing to PHH, exploration of the CSF lipid signature in relation to brain pathology is of interest. Despite being a relatively new addition to the omic’s landscape, lipidomics are increasingly recognized as a tool for biomarker identification, as they provide a comprehensive overview of lipid profiles in biological systems. We here employ an untargeted mass spectroscopy-based platform and reveal the complete lipid profile of cisternal CSF from healthy control subjects and demonstrate its bimodal fluctuation with age. Various classes of lipids, in addition to select individual lipids, were elevated in the ventricular CSF obtained from patients with SAH during placement of an external ventricular drain. The lipidomic signature of the CSF in the patients with SAH suggests dysregulation of the lipids in the CSF in this patient group. Our data thereby reveal possible biomarkers present in a brain pathology with a hemorrhagic event, some of which could be potential future biomarkers for hypersecretion contributing to ventriculomegaly and thus pharmacological targets for pathologies involving disturbed CSF dynamics.
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spelling pubmed-105259232023-09-28 Distinct Cerebrospinal Fluid Lipid Signature in Patients with Subarachnoid Hemorrhage-Induced Hydrocephalus Toft-Bertelsen, Trine L. Andreassen, Søren Norge Rostgaard, Nina Olsen, Markus Harboe Norager, Nicolas H. Capion, Tenna Juhler, Marianne MacAulay, Nanna Biomedicines Article Patients with subarachnoid hemorrhage (SAH) may develop posthemorrhagic hydrocephalus (PHH), which is treated with surgical cerebrospinal fluid (CSF) diversion. This diversion is associated with risk of infection and shunt failure. Biomarkers for PHH etiology, CSF dynamics disturbances, and potentially subsequent shunt dependency are therefore in demand. With the recent demonstration of lipid-mediated CSF hypersecretion contributing to PHH, exploration of the CSF lipid signature in relation to brain pathology is of interest. Despite being a relatively new addition to the omic’s landscape, lipidomics are increasingly recognized as a tool for biomarker identification, as they provide a comprehensive overview of lipid profiles in biological systems. We here employ an untargeted mass spectroscopy-based platform and reveal the complete lipid profile of cisternal CSF from healthy control subjects and demonstrate its bimodal fluctuation with age. Various classes of lipids, in addition to select individual lipids, were elevated in the ventricular CSF obtained from patients with SAH during placement of an external ventricular drain. The lipidomic signature of the CSF in the patients with SAH suggests dysregulation of the lipids in the CSF in this patient group. Our data thereby reveal possible biomarkers present in a brain pathology with a hemorrhagic event, some of which could be potential future biomarkers for hypersecretion contributing to ventriculomegaly and thus pharmacological targets for pathologies involving disturbed CSF dynamics. MDPI 2023-08-23 /pmc/articles/PMC10525923/ /pubmed/37760800 http://dx.doi.org/10.3390/biomedicines11092360 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Toft-Bertelsen, Trine L.
Andreassen, Søren Norge
Rostgaard, Nina
Olsen, Markus Harboe
Norager, Nicolas H.
Capion, Tenna
Juhler, Marianne
MacAulay, Nanna
Distinct Cerebrospinal Fluid Lipid Signature in Patients with Subarachnoid Hemorrhage-Induced Hydrocephalus
title Distinct Cerebrospinal Fluid Lipid Signature in Patients with Subarachnoid Hemorrhage-Induced Hydrocephalus
title_full Distinct Cerebrospinal Fluid Lipid Signature in Patients with Subarachnoid Hemorrhage-Induced Hydrocephalus
title_fullStr Distinct Cerebrospinal Fluid Lipid Signature in Patients with Subarachnoid Hemorrhage-Induced Hydrocephalus
title_full_unstemmed Distinct Cerebrospinal Fluid Lipid Signature in Patients with Subarachnoid Hemorrhage-Induced Hydrocephalus
title_short Distinct Cerebrospinal Fluid Lipid Signature in Patients with Subarachnoid Hemorrhage-Induced Hydrocephalus
title_sort distinct cerebrospinal fluid lipid signature in patients with subarachnoid hemorrhage-induced hydrocephalus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10525923/
https://www.ncbi.nlm.nih.gov/pubmed/37760800
http://dx.doi.org/10.3390/biomedicines11092360
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