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CSF Proteomics of Patients with Hydrocephalus and Subarachnoid Haemorrhage

BACKGROUND: The pathophysiology of brain injury following aneurysmal subarachnoid haemorrhage (SAH) is associated with numerous mediators. The aim of the study is to analyse protein changes after SAH in cerebrospinal fluid (CSF) using mass spectrometry (MS). METHODS: CSF samples were obtained from f...

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Autores principales: Sokół, Bartosz, Urbaniak, Bartosz, Zaremba, Bartosz, Wąsik, Norbert, Kokot, Zenon J., Jankowski, Roman
Formato: Online Artículo Texto
Lenguaje:English
Publicado: De Gruyter 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6778397/
https://www.ncbi.nlm.nih.gov/pubmed/31637049
http://dx.doi.org/10.1515/tnsci-2019-0040
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author Sokół, Bartosz
Urbaniak, Bartosz
Zaremba, Bartosz
Wąsik, Norbert
Kokot, Zenon J.
Jankowski, Roman
author_facet Sokół, Bartosz
Urbaniak, Bartosz
Zaremba, Bartosz
Wąsik, Norbert
Kokot, Zenon J.
Jankowski, Roman
author_sort Sokół, Bartosz
collection PubMed
description BACKGROUND: The pathophysiology of brain injury following aneurysmal subarachnoid haemorrhage (SAH) is associated with numerous mediators. The aim of the study is to analyse protein changes after SAH in cerebrospinal fluid (CSF) using mass spectrometry (MS). METHODS: CSF samples were obtained from forty-four control subjects, seven good outcome and ten poor outcome SAH patients. CSF samples were collected at specific time intervals after SAH (days 1, 5 and 10). MALDI-TOF (Matrix Assisted Laser Desorption/Ionization Time-of-Flight) and ClinProTools software were utilised for MS, MS/MS (Mass Spectrometry) spectra collection and analysis. Selected masses were identified. The MALDI-TOF profiling experiments allowed for the targeted selection of potential markers in SAH. The study was performed in three steps by comparison of CSF samples: (1) from the control group and SAH patients (both good and poor outcome groups); (2) collected on days 1, 5 and 10 within the groups of poor SAH and good SAH patients, respectively; (3) from poor outcome SAH and good outcome patients at days 1, 5 and 10. RESULTS: 15 new proteins whose CSF level is alternated by SAH presence, SAH treatment outcome and time passed since aneurysm rupture were identified. CONCLUSIONS: We demonstrated new proteins which might play a role in different stages of subarachnoid haemorrhage and could be a new target for further investigation.
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spelling pubmed-67783972019-10-21 CSF Proteomics of Patients with Hydrocephalus and Subarachnoid Haemorrhage Sokół, Bartosz Urbaniak, Bartosz Zaremba, Bartosz Wąsik, Norbert Kokot, Zenon J. Jankowski, Roman Transl Neurosci Regular Articles BACKGROUND: The pathophysiology of brain injury following aneurysmal subarachnoid haemorrhage (SAH) is associated with numerous mediators. The aim of the study is to analyse protein changes after SAH in cerebrospinal fluid (CSF) using mass spectrometry (MS). METHODS: CSF samples were obtained from forty-four control subjects, seven good outcome and ten poor outcome SAH patients. CSF samples were collected at specific time intervals after SAH (days 1, 5 and 10). MALDI-TOF (Matrix Assisted Laser Desorption/Ionization Time-of-Flight) and ClinProTools software were utilised for MS, MS/MS (Mass Spectrometry) spectra collection and analysis. Selected masses were identified. The MALDI-TOF profiling experiments allowed for the targeted selection of potential markers in SAH. The study was performed in three steps by comparison of CSF samples: (1) from the control group and SAH patients (both good and poor outcome groups); (2) collected on days 1, 5 and 10 within the groups of poor SAH and good SAH patients, respectively; (3) from poor outcome SAH and good outcome patients at days 1, 5 and 10. RESULTS: 15 new proteins whose CSF level is alternated by SAH presence, SAH treatment outcome and time passed since aneurysm rupture were identified. CONCLUSIONS: We demonstrated new proteins which might play a role in different stages of subarachnoid haemorrhage and could be a new target for further investigation. De Gruyter 2019-10-02 /pmc/articles/PMC6778397/ /pubmed/31637049 http://dx.doi.org/10.1515/tnsci-2019-0040 Text en © 2019 Bartosz Sokół et al. published by De Gruyter http://creativecommons.org/licenses/by/4.0 This work is licensed under the Creative Commons Attribution 4.0 Public License.
spellingShingle Regular Articles
Sokół, Bartosz
Urbaniak, Bartosz
Zaremba, Bartosz
Wąsik, Norbert
Kokot, Zenon J.
Jankowski, Roman
CSF Proteomics of Patients with Hydrocephalus and Subarachnoid Haemorrhage
title CSF Proteomics of Patients with Hydrocephalus and Subarachnoid Haemorrhage
title_full CSF Proteomics of Patients with Hydrocephalus and Subarachnoid Haemorrhage
title_fullStr CSF Proteomics of Patients with Hydrocephalus and Subarachnoid Haemorrhage
title_full_unstemmed CSF Proteomics of Patients with Hydrocephalus and Subarachnoid Haemorrhage
title_short CSF Proteomics of Patients with Hydrocephalus and Subarachnoid Haemorrhage
title_sort csf proteomics of patients with hydrocephalus and subarachnoid haemorrhage
topic Regular Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6778397/
https://www.ncbi.nlm.nih.gov/pubmed/31637049
http://dx.doi.org/10.1515/tnsci-2019-0040
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