Drug-resistant focal epilepsy in children is associated with increased modal controllability of the whole brain and epileptogenic regions.
Drug-resistant focal epilepsy in children is associated with increased modal controllability of the whole brain and epileptogenic regions.
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DOI:
10.1038/s42003-022-03342-8
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发表时间:
2022-04-28
影响因子:
5.9
通讯作者:
中科院分区:
文献类型:
--
作者:
Network control theory provides a framework by which neurophysiological dynamics of the brain can be modelled as a function of the structural connectome constructed from diffusion MRI. Average controllability describes the ability of a region to drive the brain to easy-to-reach neurophysiological states whilst modal controllability describes the ability of a region to drive the brain to difficult-to-reach states. In this study, we identify increases in mean average and modal controllability in children with drug-resistant epilepsy compared to healthy controls. Using simulations, we purport that these changes may be a result of increased thalamocortical connectivity. At the node level, we demonstrate decreased modal controllability in the thalamus and posterior cingulate regions. In those undergoing resective surgery, we also demonstrate increased modal controllability of the resected parcels, a finding specific to patients who were rendered seizure free following surgery. Changes in controllability are a manifestation of brain network dysfunction in epilepsy and may be a useful construct to understand the pathophysiology of this archetypical network disease. Understanding the mechanisms underlying these controllability changes may also facilitate the design of network-focussed interventions that seek to normalise network structure and function. Children with drug-resistant epilepsy exhibit distinct structural connectomes and changes in network controllability from healthy controls, providing further insight into the pathophysiology of this disease.
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影响因子:
3.5
作者:
Gorgolewski K;Burns CD;Madison C;Clark D;Halchenko YO;Waskom ML;Ghosh SS
通讯作者:
Ghosh SS
影响因子:
3.7
作者:
Goñi J;Avena-Koenigsberger A;Velez de Mendizabal N;van den Heuvel MP;Betzel RF;Sporns O
通讯作者:
Sporns O
影响因子:
2.6
作者:
HAMDAN, AMA;NAYFEH, AH
通讯作者:
NAYFEH, AH
影响因子:
--
作者:
Blumenfeld, H
通讯作者:
Blumenfeld, H
影响因子:
25
作者:
Dworkin, Jordan D.;Linn, Kristin A.;Bassett, Danielle S.
通讯作者:
Bassett, Danielle S.