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Quantifying cerebrospinal fluid dynamics: A review of human neuroimaging contributions to CSF physiology and neurodegenerative disease

Cerebrospinal fluid (CSF), predominantly produced in the ventricles and circulating throughout the brain and spinal cord, is a key protective mechanism of the central nervous system (CNS). Physical cushioning, nutrient delivery, metabolic waste, including protein clearance, are key functions of the...

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Autores principales: Mehta, Neel H., Suss, Richard A., Dyke, Jonathan P., Theise, Neil D., Chiang, Gloria C., Strauss, Sara, Saint-Louis, Leslie, Li, Yi, Pahlajani, Silky, Babaria, Vivek, Glodzik, Lidia, Carare, Roxana O., de Leon, Mony J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9987579/
https://www.ncbi.nlm.nih.gov/pubmed/35643187
http://dx.doi.org/10.1016/j.nbd.2022.105776
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author Mehta, Neel H.
Suss, Richard A.
Dyke, Jonathan P.
Theise, Neil D.
Chiang, Gloria C.
Strauss, Sara
Saint-Louis, Leslie
Li, Yi
Pahlajani, Silky
Babaria, Vivek
Glodzik, Lidia
Carare, Roxana O.
de Leon, Mony J.
author_facet Mehta, Neel H.
Suss, Richard A.
Dyke, Jonathan P.
Theise, Neil D.
Chiang, Gloria C.
Strauss, Sara
Saint-Louis, Leslie
Li, Yi
Pahlajani, Silky
Babaria, Vivek
Glodzik, Lidia
Carare, Roxana O.
de Leon, Mony J.
author_sort Mehta, Neel H.
collection PubMed
description Cerebrospinal fluid (CSF), predominantly produced in the ventricles and circulating throughout the brain and spinal cord, is a key protective mechanism of the central nervous system (CNS). Physical cushioning, nutrient delivery, metabolic waste, including protein clearance, are key functions of the CSF in humans. CSF volume and flow dynamics regulate intracranial pressure and are fundamental to diagnosing disorders including normal pressure hydrocephalus, intracranial hypotension, CSF leaks, and possibly Alzheimer’s disease (AD). The ability of CSF to clear normal and pathological proteins, such as amyloid-beta (Aβ), tau, alpha synuclein and others, implicates it production, circulation, and composition, in many neuropathologies. Several neuroimaging modalities have been developed to probe CSF fluid dynamics and better relate CSF volume and flow to anatomy and clinical conditions. Approaches include 2-photon microscopic techniques, MRI (tracer-based, gadolinium contrast, endogenous phase-contrast), and dynamic positron emission tomography (PET) using existing approved radiotracers. Here, we discuss CSF flow neuroimaging, from animal models to recent clinical-research advances, summarizing current endeavors to quantify and map CSF flow with implications towards pathophysiology, new biomarkers, and treatments of neurological diseases.
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spelling pubmed-99875792023-03-06 Quantifying cerebrospinal fluid dynamics: A review of human neuroimaging contributions to CSF physiology and neurodegenerative disease Mehta, Neel H. Suss, Richard A. Dyke, Jonathan P. Theise, Neil D. Chiang, Gloria C. Strauss, Sara Saint-Louis, Leslie Li, Yi Pahlajani, Silky Babaria, Vivek Glodzik, Lidia Carare, Roxana O. de Leon, Mony J. Neurobiol Dis Article Cerebrospinal fluid (CSF), predominantly produced in the ventricles and circulating throughout the brain and spinal cord, is a key protective mechanism of the central nervous system (CNS). Physical cushioning, nutrient delivery, metabolic waste, including protein clearance, are key functions of the CSF in humans. CSF volume and flow dynamics regulate intracranial pressure and are fundamental to diagnosing disorders including normal pressure hydrocephalus, intracranial hypotension, CSF leaks, and possibly Alzheimer’s disease (AD). The ability of CSF to clear normal and pathological proteins, such as amyloid-beta (Aβ), tau, alpha synuclein and others, implicates it production, circulation, and composition, in many neuropathologies. Several neuroimaging modalities have been developed to probe CSF fluid dynamics and better relate CSF volume and flow to anatomy and clinical conditions. Approaches include 2-photon microscopic techniques, MRI (tracer-based, gadolinium contrast, endogenous phase-contrast), and dynamic positron emission tomography (PET) using existing approved radiotracers. Here, we discuss CSF flow neuroimaging, from animal models to recent clinical-research advances, summarizing current endeavors to quantify and map CSF flow with implications towards pathophysiology, new biomarkers, and treatments of neurological diseases. 2022-08 2022-05-25 /pmc/articles/PMC9987579/ /pubmed/35643187 http://dx.doi.org/10.1016/j.nbd.2022.105776 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ).
spellingShingle Article
Mehta, Neel H.
Suss, Richard A.
Dyke, Jonathan P.
Theise, Neil D.
Chiang, Gloria C.
Strauss, Sara
Saint-Louis, Leslie
Li, Yi
Pahlajani, Silky
Babaria, Vivek
Glodzik, Lidia
Carare, Roxana O.
de Leon, Mony J.
Quantifying cerebrospinal fluid dynamics: A review of human neuroimaging contributions to CSF physiology and neurodegenerative disease
title Quantifying cerebrospinal fluid dynamics: A review of human neuroimaging contributions to CSF physiology and neurodegenerative disease
title_full Quantifying cerebrospinal fluid dynamics: A review of human neuroimaging contributions to CSF physiology and neurodegenerative disease
title_fullStr Quantifying cerebrospinal fluid dynamics: A review of human neuroimaging contributions to CSF physiology and neurodegenerative disease
title_full_unstemmed Quantifying cerebrospinal fluid dynamics: A review of human neuroimaging contributions to CSF physiology and neurodegenerative disease
title_short Quantifying cerebrospinal fluid dynamics: A review of human neuroimaging contributions to CSF physiology and neurodegenerative disease
title_sort quantifying cerebrospinal fluid dynamics: a review of human neuroimaging contributions to csf physiology and neurodegenerative disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9987579/
https://www.ncbi.nlm.nih.gov/pubmed/35643187
http://dx.doi.org/10.1016/j.nbd.2022.105776
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