The impact of brain lesions on tDCS-induced electric fields

被引:3
|
作者
Evans, Carys [1 ]
Johnstone, Ainslie [1 ]
Zich, Catharina [1 ,2 ]
Lee, Jenny S. A. [1 ]
Ward, Nick S. [1 ,3 ,4 ]
Bestmann, Sven [1 ,5 ]
机构
[1] UCL, UCL Queen Sq Inst Neurol, Dept Clin & Movement Neurosci, London, England
[2] Univ Oxford, Wellcome Ctr Integrat Neuroimaging, Nuffield Dept Clin Neurosci, FMRIB, Oxford, Oxfordshire, England
[3] Natl Hosp Neurol & Neurosurg, London, England
[4] UCLP Ctr Neurorehabil, London, England
[5] UCL, UCL Queen Sq Inst Neurol, Wellcome Ctr Human Neuroimaging, London, England
基金
英国惠康基金;
关键词
DIRECT-CURRENT STIMULATION; ISCHEMIC-STROKE; TISSUE; RECOVERY; APHASIA; REHABILITATION; EXCITABILITY; METAANALYSIS; VARIABILITY;
D O I
10.1038/s41598-023-45905-7
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
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页数:15
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