Motor Cortical Network Flexibility is Associated With Biomechanical Walking Impairment in Chronic Stroke.
Motor Cortical Network Flexibility is Associated With Biomechanical Walking Impairment in Chronic Stroke.
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DOI:
10.1177/15459683211046272
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发表时间:
2021-12
影响因子:
4.2
通讯作者:
Borich MR
中科院分区:
文献类型:
--
作者:
Palmer JA;Kesar TM;Wolf SL;Borich MR
The inability to flexibly modulate motor behavior with changes in task demand or environmental context is a pervasive feature of motor impairment and dysfunctional mobility after stroke. The purpose of this study was to test the reactive and modulatory capacity of lower-limb primary motor cortical (M1) networks using electroencephalography (EEG) measures of cortical activity evoked by transcranial magnetic stimulation (TMS) and to evaluate their associations with clinical and biomechanical measures of walking function in chronic stroke. Transcranial magnetic stimulation (TMS) assessments of motor cortex (M1) excitability were performed during rest and active ipsilateral plantarflexion in chronic stroke and age-matched controls. TMS-evoked motor cortical network interactions were quantified with simultaneous electroencephalography (EEG) as the post-TMS (0-300ms) beta (15-30Hz) coherence between electrodes overlying M1 bilaterally. We compared TMS-evoked coherence between groups during rest and active conditions and tested associations with post-stroke motor impairment, paretic propulsive gait deficits, and the presence of paretic leg motor evoked potentials (MEPs). Stroke (n=14, 66 ±9 years, F=4) showed lower TMS-evoked cortical coherence and activity-dependent modulation compared to controls (n=9, 68±6 years, F=3). Blunted and atypical modulation of TMS-evoked coherence were associated with lower paretic ankle moments for propulsive force generation during walking and absent paretic MEPs. Blunted flexibility of motor cortical networks to react to TMS and modulate during motor activity is distinctly associated with paretic limb biomechanical walking impairment, and may provide useful insight into the neuromechanistic underpinnings of chronic post-stroke mobility deficits.
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影响因子:
4.2
作者:
Bowden, Mark G.;Balasubramanian, Chitralakshmi K.;Kautz, Steven A.
通讯作者:
Kautz, Steven A.
影响因子:
4.1
作者:
Fjell, Anders M.;Walhovd, Kristine B.
通讯作者:
Walhovd, Kristine B.
影响因子:
4.2
作者:
Palmer, Jacqueline A.;Wheaton, Lewis A.;Borich, Michael R.
通讯作者:
Borich, Michael R.
影响因子:
4.7
作者:
Palmer, Jacqueline A.;Needle, Alan R.;Binder-Macleod, Stuart A.
通讯作者:
Binder-Macleod, Stuart A.
DOI:
10.1016/j.clinph.2012.01.010
发表时间:
2012-05
期刊:
Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology
影响因子:
--
作者:
Groppa S;Oliviero A;Eisen A;Quartarone A;Cohen LG;Mall V;Kaelin-Lang A;Mima T;Rossi S;Thickbroom GW;Rossini PM;Ziemann U;Valls-Solé J;Siebner HR
通讯作者:
Siebner HR