Microdialysis and microperfusion electrodes in neurologic disease monitoring.


Journal

Fluids and barriers of the CNS
ISSN: 2045-8118
Titre abrégé: Fluids Barriers CNS
Pays: England
ID NLM: 101553157

Informations de publication

Date de publication:
01 Dec 2021
Historique:
received: 07 10 2021
accepted: 23 11 2021
entrez: 2 12 2021
pubmed: 3 12 2021
medline: 22 2 2022
Statut: epublish

Résumé

Contemporary biomarker collection techniques in blood and cerebrospinal fluid have to date offered only modest clinical insights into neurologic diseases such as epilepsy and glioma. Conversely, the collection of human electroencephalography (EEG) data has long been the standard of care in these patients, enabling individualized insights for therapy and revealing fundamental principles of human neurophysiology. Increasing interest exists in simultaneously measuring neurochemical biomarkers and electrophysiological data to enhance our understanding of human disease mechanisms. This review compares microdialysis, microperfusion, and implanted EEG probe architectures and performance parameters. Invasive consequences of probe implantation are also investigated along with the functional impact of biofouling. Finally, previously developed microdialysis electrodes and microperfusion electrodes are reviewed in preclinical and clinical settings. Critically, current and precedent microdialysis and microperfusion probes lack the ability to collect neurochemical data that is spatially and temporally coincident with EEG data derived from depth electrodes. This ultimately limits diagnostic and therapeutic progress in epilepsy and glioma research. However, this gap also provides a unique opportunity to create a dual-sensing technology that will provide unprecedented insights into the pathogenic mechanisms of human neurologic disease.

Identifiants

pubmed: 34852829
doi: 10.1186/s12987-021-00292-x
pii: 10.1186/s12987-021-00292-x
pmc: PMC8638547
doi:

Substances chimiques

Biomarkers 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

52

Subventions

Organisme : NINDS NIH HHS
ID : R01 NS064571
Pays : United States
Organisme : NINDS NIH HHS
ID : R21 NS111756
Pays : United States
Organisme : NINDS NIH HHS
ID : NS111756
Pays : United States

Informations de copyright

© 2021. The Author(s).

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Auteurs

Luke A Stangler (LA)

School of Engineering, Deakin University, 3216, Geelong, Victoria, Australia.
Division of Engineering, Mayo Clinic, 55905, Rochester, MN, USA.

Abbas Kouzani (A)

School of Engineering, Deakin University, 3216, Geelong, Victoria, Australia.

Kevin E Bennet (KE)

School of Engineering, Deakin University, 3216, Geelong, Victoria, Australia.
Division of Engineering, Mayo Clinic, 55905, Rochester, MN, USA.

Ludovic Dumee (L)

School of Engineering, Deakin University, 3216, Geelong, Victoria, Australia.

Michael Berk (M)

School of Medicine, Deakin University, 3216, Geelong, Victoria, Australia.

Gregory A Worrell (GA)

Department of Neurology, Mayo Clinic, 55905, Rochester, MN, USA.

Steven Steele (S)

Division of Engineering, Mayo Clinic, 55905, Rochester, MN, USA.

Terence C Burns (TC)

Department of Neurosurgery, Mayo Clinic, 55905, Rochester, MN, USA.

Charles L Howe (CL)

Department of Neurology, Mayo Clinic, 55905, Rochester, MN, USA. howe@mayo.edu.
Division of Experimental Neurology, Mayo Clinic, 55905, Rochester, MN, USA. howe@mayo.edu.
Center for MS and Autoimmune Neurology, Mayo Clinic, 55905, Rochester, MN, USA. howe@mayo.edu.

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