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Liquid biopsies in epilepsy: biomarkers for etiology, diagnosis, prognosis, and therapeutics

Epilepsy is one of the most common diseases of the central nervous system, impacting nearly 50 million people around the world. Heterogeneous in nature, epilepsy presents in children and adults alike. Currently, surgery is one treatment approach that can completely cure epilepsy. However, not all in...

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Autores principales: Whitlock, Jordan H., Soelter, Tabea M., Williams, Avery S., Hardigan, Andrew A., Lasseigne, Brittany N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Singapore 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8732818/
https://www.ncbi.nlm.nih.gov/pubmed/34694568
http://dx.doi.org/10.1007/s13577-021-00624-x
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author Whitlock, Jordan H.
Soelter, Tabea M.
Williams, Avery S.
Hardigan, Andrew A.
Lasseigne, Brittany N.
author_facet Whitlock, Jordan H.
Soelter, Tabea M.
Williams, Avery S.
Hardigan, Andrew A.
Lasseigne, Brittany N.
author_sort Whitlock, Jordan H.
collection PubMed
description Epilepsy is one of the most common diseases of the central nervous system, impacting nearly 50 million people around the world. Heterogeneous in nature, epilepsy presents in children and adults alike. Currently, surgery is one treatment approach that can completely cure epilepsy. However, not all individuals are eligible for surgical procedures or have successful outcomes. In addition to surgical approaches, antiepileptic drugs (AEDs) have also allowed individuals with epilepsy to achieve freedom from seizures. Others have found treatment through nonpharmacologic approaches such as vagus nerve stimulation, or responsive neurostimulation. Difficulty in accessing samples of human brain tissue along with advances in sequencing technology have driven researchers to investigate sampling liquid biopsies in blood, serum, plasma, and cerebrospinal fluid within the context of epilepsy. Liquid biopsies provide minimal or non-invasive sample collection approaches and can be assayed relatively easily across multiple time points, unlike tissue-based sampling. Various efforts have investigated circulating nucleic acids from these samples including microRNAs, cell-free DNA, transfer RNAs, and long non-coding RNAs. Here, we review nucleic acid-based liquid biopsies in epilepsy to improve understanding of etiology, diagnosis, prediction, and therapeutic monitoring.
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spelling pubmed-87328182022-01-18 Liquid biopsies in epilepsy: biomarkers for etiology, diagnosis, prognosis, and therapeutics Whitlock, Jordan H. Soelter, Tabea M. Williams, Avery S. Hardigan, Andrew A. Lasseigne, Brittany N. Hum Cell Review Article Epilepsy is one of the most common diseases of the central nervous system, impacting nearly 50 million people around the world. Heterogeneous in nature, epilepsy presents in children and adults alike. Currently, surgery is one treatment approach that can completely cure epilepsy. However, not all individuals are eligible for surgical procedures or have successful outcomes. In addition to surgical approaches, antiepileptic drugs (AEDs) have also allowed individuals with epilepsy to achieve freedom from seizures. Others have found treatment through nonpharmacologic approaches such as vagus nerve stimulation, or responsive neurostimulation. Difficulty in accessing samples of human brain tissue along with advances in sequencing technology have driven researchers to investigate sampling liquid biopsies in blood, serum, plasma, and cerebrospinal fluid within the context of epilepsy. Liquid biopsies provide minimal or non-invasive sample collection approaches and can be assayed relatively easily across multiple time points, unlike tissue-based sampling. Various efforts have investigated circulating nucleic acids from these samples including microRNAs, cell-free DNA, transfer RNAs, and long non-coding RNAs. Here, we review nucleic acid-based liquid biopsies in epilepsy to improve understanding of etiology, diagnosis, prediction, and therapeutic monitoring. Springer Singapore 2021-10-25 2022 /pmc/articles/PMC8732818/ /pubmed/34694568 http://dx.doi.org/10.1007/s13577-021-00624-x 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 Review Article
Whitlock, Jordan H.
Soelter, Tabea M.
Williams, Avery S.
Hardigan, Andrew A.
Lasseigne, Brittany N.
Liquid biopsies in epilepsy: biomarkers for etiology, diagnosis, prognosis, and therapeutics
title Liquid biopsies in epilepsy: biomarkers for etiology, diagnosis, prognosis, and therapeutics
title_full Liquid biopsies in epilepsy: biomarkers for etiology, diagnosis, prognosis, and therapeutics
title_fullStr Liquid biopsies in epilepsy: biomarkers for etiology, diagnosis, prognosis, and therapeutics
title_full_unstemmed Liquid biopsies in epilepsy: biomarkers for etiology, diagnosis, prognosis, and therapeutics
title_short Liquid biopsies in epilepsy: biomarkers for etiology, diagnosis, prognosis, and therapeutics
title_sort liquid biopsies in epilepsy: biomarkers for etiology, diagnosis, prognosis, and therapeutics
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8732818/
https://www.ncbi.nlm.nih.gov/pubmed/34694568
http://dx.doi.org/10.1007/s13577-021-00624-x
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