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Transcranial magnetic stimulation as a tool to understand genetic conditions associated with epilepsy
Advances in genetics may enable a deeper understanding of disease mechanisms and promote a shift to more personalised medicine in the epilepsies. At present, understanding of consequences of genetic variants mainly relies on preclinical functional work; tools for acquiring similar data from the livi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8432162/ https://www.ncbi.nlm.nih.gov/pubmed/32783192 http://dx.doi.org/10.1111/epi.16634 |
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author | Silvennoinen, Katri Balestrini, Simona Rothwell, John C. Sisodiya, Sanjay M. |
author_facet | Silvennoinen, Katri Balestrini, Simona Rothwell, John C. Sisodiya, Sanjay M. |
author_sort | Silvennoinen, Katri |
collection | PubMed |
description | Advances in genetics may enable a deeper understanding of disease mechanisms and promote a shift to more personalised medicine in the epilepsies. At present, understanding of consequences of genetic variants mainly relies on preclinical functional work; tools for acquiring similar data from the living human brain are needed. Transcranial magnetic stimulation (TMS), in particular paired‐pulse TMS protocols which depend on the function of cortical GABAergic interneuron networks, has the potential to become such a tool. For this report, we identified and reviewed 23 publications on TMS studies of cortical excitability and inhibition in 15 different genes or conditions relevant to epilepsy. Reduced short‐interval intracortical inhibition (SICI) and reduced cortical silent period (CSP) duration were the most commonly reported findings, suggesting abnormal GABA(A)‐ (SICI) or GABA(B)ergic (CSP) signalling. For several conditions, these findings are plausible based on established evidence of involvement of the GABAergic system; for some others, they may inform future research around such mechanisms. Challenges of TMS include lack of complete understanding of the neural underpinnings of the measures used: hypotheses and analyses should be based on existing clinical and preclinical data. Further pitfalls include gathering sufficient numbers of participants, and the effect of confounding factors, especially medications. TMS‐EEG is a unique perturbational technique to study the intrinsic properties of the cortex with excellent temporal resolution; while it has the potential to provide further information of use in interpreting effects of genetic variants, currently the links between measures and neurophysiology are less established. Despite these challenges, TMS is a tool with potential for elucidating the system‐level in vivo functional consequences of genetic variants in people carrying genetic changes of interest, providing unique insights. |
format | Online Article Text |
id | pubmed-8432162 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84321622021-09-14 Transcranial magnetic stimulation as a tool to understand genetic conditions associated with epilepsy Silvennoinen, Katri Balestrini, Simona Rothwell, John C. Sisodiya, Sanjay M. Epilepsia Critical Review and Invited Commentary Advances in genetics may enable a deeper understanding of disease mechanisms and promote a shift to more personalised medicine in the epilepsies. At present, understanding of consequences of genetic variants mainly relies on preclinical functional work; tools for acquiring similar data from the living human brain are needed. Transcranial magnetic stimulation (TMS), in particular paired‐pulse TMS protocols which depend on the function of cortical GABAergic interneuron networks, has the potential to become such a tool. For this report, we identified and reviewed 23 publications on TMS studies of cortical excitability and inhibition in 15 different genes or conditions relevant to epilepsy. Reduced short‐interval intracortical inhibition (SICI) and reduced cortical silent period (CSP) duration were the most commonly reported findings, suggesting abnormal GABA(A)‐ (SICI) or GABA(B)ergic (CSP) signalling. For several conditions, these findings are plausible based on established evidence of involvement of the GABAergic system; for some others, they may inform future research around such mechanisms. Challenges of TMS include lack of complete understanding of the neural underpinnings of the measures used: hypotheses and analyses should be based on existing clinical and preclinical data. Further pitfalls include gathering sufficient numbers of participants, and the effect of confounding factors, especially medications. TMS‐EEG is a unique perturbational technique to study the intrinsic properties of the cortex with excellent temporal resolution; while it has the potential to provide further information of use in interpreting effects of genetic variants, currently the links between measures and neurophysiology are less established. Despite these challenges, TMS is a tool with potential for elucidating the system‐level in vivo functional consequences of genetic variants in people carrying genetic changes of interest, providing unique insights. John Wiley and Sons Inc. 2020-08-12 2020-09 /pmc/articles/PMC8432162/ /pubmed/32783192 http://dx.doi.org/10.1111/epi.16634 Text en © 2020 The Authors. Epilepsia published by Wiley Periodicals LLC on behalf of International League Against Epilepsy https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Critical Review and Invited Commentary Silvennoinen, Katri Balestrini, Simona Rothwell, John C. Sisodiya, Sanjay M. Transcranial magnetic stimulation as a tool to understand genetic conditions associated with epilepsy |
title | Transcranial magnetic stimulation as a tool to understand genetic conditions associated with epilepsy |
title_full | Transcranial magnetic stimulation as a tool to understand genetic conditions associated with epilepsy |
title_fullStr | Transcranial magnetic stimulation as a tool to understand genetic conditions associated with epilepsy |
title_full_unstemmed | Transcranial magnetic stimulation as a tool to understand genetic conditions associated with epilepsy |
title_short | Transcranial magnetic stimulation as a tool to understand genetic conditions associated with epilepsy |
title_sort | transcranial magnetic stimulation as a tool to understand genetic conditions associated with epilepsy |
topic | Critical Review and Invited Commentary |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8432162/ https://www.ncbi.nlm.nih.gov/pubmed/32783192 http://dx.doi.org/10.1111/epi.16634 |
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