BOČKOVÁ, Martina, Eva VÝTVAROVÁ, Martin LAMOŠ, P. KLIMES, P. JURAK, J. HALAMEK, Sabina GOLDEMUNDOVÁ, Marek BALÁŽ and Ivan REKTOR. Cortical network organization reflects clinical response to subthalamic nucleus deep brain stimulation in Parkinson's disease. Human Brain mapping. Hoboken: WILEY-BLACKWELL, 2021, vol. 42, No 17, p. 5626-5635. ISSN 1065-9471. Available from: https://dx.doi.org/10.1002/hbm.25642.
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Basic information
Original name Cortical network organization reflects clinical response to subthalamic nucleus deep brain stimulation in Parkinson's disease
Authors BOČKOVÁ, Martina (203 Czech Republic, belonging to the institution), Eva VÝTVAROVÁ (203 Czech Republic, belonging to the institution), Martin LAMOŠ (203 Czech Republic, belonging to the institution), P. KLIMES, P. JURAK, J. HALAMEK, Sabina GOLDEMUNDOVÁ (203 Czech Republic, belonging to the institution), Marek BALÁŽ (703 Slovakia, belonging to the institution) and Ivan REKTOR (203 Czech Republic, guarantor, belonging to the institution).
Edition Human Brain mapping, Hoboken, WILEY-BLACKWELL, 2021, 1065-9471.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 30103 Neurosciences
Country of publisher Netherlands
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 5.399
RIV identification code RIV/00216224:14740/21:00119591
Organization unit Central European Institute of Technology
Doi http://dx.doi.org/10.1002/hbm.25642
UT WoS 000689718000001
Keywords in English deep brain stimulation; high-density EEG; network analysis; subthalamic nucleus
Tags 14110127, CF MAFIL, podil, rivok
Tags International impact, Reviewed
Changed by Changed by: Mgr. Pavla Foltynová, Ph.D., učo 106624. Changed: 18/1/2022 14:20.
Abstract
The degree of response to subthalamic nucleus deep brain stimulation (STN-DBS) is individual and hardly predictable. We hypothesized that DBS-related changes in cortical network organization are related to the clinical effect. Network analysis based on graph theory was used to evaluate the high-density electroencephalography (HDEEG) recorded during a visual three-stimuli paradigm in 32 Parkinson's disease (PD) patients treated by STN-DBS in stimulation "off" and "on" states. Preprocessed scalp data were reconstructed into the source space and correlated to the behavioral parameters. In the majority of patients (n = 26), STN-DBS did not lead to changes in global network organization in large-scale brain networks. In a subgroup of suboptimal responders (n = 6), identified according to reaction times (RT) and clinical parameters (lower Unified Parkinson's Disease Rating Scale [UPDRS] score improvement after DBS and worse performance in memory tests), decreased global connectivity in the 1-8 Hz frequency range and regional node strength in frontal areas were detected. The important role of the supplementary motor area for the optimal DBS response was demonstrated by the increased node strength and eigenvector centrality in good responders. This response was missing in the suboptimal responders. Cortical topologic architecture is modified by the response to STN-DBS leading to a dysfunction of the large-scale networks in suboptimal responders.
Links
GA21-25953S, research and development projectName: Subkortikální jádra a kortikální funkce z perspektivy hluboké mozkové stimulace (Acronym: DBS3D)
Investor: Czech Science Foundation, Subcortical nuclei and cortical functions – insight from the deep brain stimulation perspective
LM2018129, research and development projectName: Národní infrastruktura pro biologické a medicínské zobrazování Czech-BioImaging
Investor: Ministry of Education, Youth and Sports of the CR
NU21-04-00445, research and development projectName: Klinická odpovídavost na STN-DBS u Parkinsonovy nemoci: vliv vaskulárních, kardiovaskulárních, metabolických a zánětlivých komorbidit (Acronym: DBScomorbidities)
Investor: Ministry of Health of the CR, STN-DBS outcomes in Parkinson´s disease: the influence of vascular, cardiovascular, metabolic, and inflammatory co-morbidities., Subprogram 1 - standard
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