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The impact of brain lesions on tDCS-induced electric fields

Abstract:
Transcranial direct current stimulation (tDCS) can enhance motor and language rehabilitation after stroke. Though brain lesions distort tDCS-induced electric field (E-field), systematic accounts remain limited. Using electric field modelling, we investigated the effect of 630 synthetic lesions on E-field magnitude in the region of interest (ROI). Models were conducted for two tDCS montages targeting either primary motor cortex (M1) or Broca's area (BA44). Absolute E-field magnitude in the ROI differed by up to 42% compared to the non-lesioned brain depending on lesion size, lesion-ROI distance, and lesion conductivity value. Lesion location determined the sign of this difference: lesions in-line with the predominant direction of current increased E-field magnitude in the ROI, whereas lesions located in the opposite direction decreased E-field magnitude. We further explored how individualised tDCS can control lesion-induced effects on E-field. Lesions affected the individualised electrode configuration needed to maximise E-field magnitude in the ROI, but this effect was negligible when prioritising the maximisation of radial inward current. Lesions distorting tDCS-induced E-field, is likely to exacerbate inter-individual variability in E-field magnitude. Individualising electrode configuration and stimulator output can minimise lesion-induced variability but requires improved estimates of lesion conductivity. Individualised tDCS is critical to overcome E-field variability in lesioned brains.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1038/s41598-023-45905-7

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Role:
Author
ORCID:
0000-0002-2306-3368
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Role:
Author
ORCID:
0000-0001-9564-6290
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Institution:
University of Oxford
Role:
Author
ORCID:
0000-0002-0705-9297
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Role:
Author
ORCID:
0000-0002-7688-9649


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Funder identifier:
10.13039/100010269
Grant:
203147/Z/16/Z
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Funder identifier:
10.13039/501100000377
Grant:
RPGF1810\93
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Funder identifier:
10.13039/100013790
Grant:
201617-03


Publisher:
Nature Research
Journal:
Scientific Reports More from this journal
Volume:
13
Issue:
1
Pages:
19430-19430
Article number:
19430
Publication date:
2023-11-08
DOI:
EISSN:
2045-2322
ISSN:
2045-2322


Language:
English
Keywords:
Pubs id:
1564840
Local pid:
pubs:1564840
Source identifiers:
W4388487027
Deposit date:
2026-06-01
ARK identifier:
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