-
Something wrong with this record ?
Resting-state functional magnetic resonance imaging of the subthalamic microlesion and stimulation effects in Parkinson's disease: Indications of a principal role of the brainstem
Š. Holiga, K. Mueller, HE. Möller, D. Urgošík, E. Růžička, ML. Schroeter, R. Jech,
Language English Country Netherlands
Document type Journal Article, Research Support, Non-U.S. Gov't
Grant support
NT12282
MZ0
CEP Register
Digital library NLK
Full text - Article
Source
NLK
Directory of Open Access Journals
from 2012
Free Medical Journals
from 2012
PubMed Central
from 2012
Europe PubMed Central
from 2012 to 2020
Open Access Digital Library
from 2012-01-01
Open Access Digital Library
from 2012-01-01
Open Access Digital Library
from 2012-01-01
ROAD: Directory of Open Access Scholarly Resources
from 2012
- MeSH
- Adult MeSH
- Echo-Planar Imaging MeSH
- Deep Brain Stimulation adverse effects MeSH
- Oxygen blood MeSH
- Middle Aged MeSH
- Humans MeSH
- Magnetic Resonance Imaging * MeSH
- Brain Mapping MeSH
- Brain Stem blood supply physiology MeSH
- Subthalamic Nucleus blood supply pathology MeSH
- Rest * MeSH
- Parkinson Disease * pathology physiopathology therapy MeSH
- Image Processing, Computer-Assisted MeSH
- Severity of Illness Index MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
During implantation of deep-brain stimulation (DBS) electrodes in the target structure, neurosurgeons and neurologists commonly observe a "microlesion effect" (MLE), which occurs well before initiating subthalamic DBS. This phenomenon typically leads to a transitory improvement of motor symptoms of patients suffering from Parkinson's disease (PD). Mechanisms behind MLE remain poorly understood. In this work, we exploited the notion of ranking to assess spontaneous brain activity in PD patients examined by resting-state functional magnetic resonance imaging in response to penetration of DBS electrodes in the subthalamic nucleus. In particular, we employed a hypothesis-free method, eigenvector centrality (EC), to reveal motor-communication-hubs of the highest rank and their reorganization following the surgery; providing a unique opportunity to evaluate the direct impact of disrupting the PD motor circuitry in vivo without prior assumptions. Penetration of electrodes was associated with increased EC of functional connectivity in the brainstem. Changes in connectivity were quantitatively related to motor improvement, which further emphasizes the clinical importance of the functional integrity of the brainstem. Surprisingly, MLE and DBS were associated with anatomically different EC maps despite their similar clinical benefit on motor functions. The DBS solely caused an increase in connectivity of the left premotor region suggesting separate pathophysiological mechanisms of both interventions. While the DBS acts at the cortical level suggesting compensatory activation of less affected motor regions, the MLE affects more fundamental circuitry as the dysfunctional brainstem predominates in the beginning of PD. These findings invigorate the overlooked brainstem perspective in the understanding of PD and support the current trend towards its early diagnosis.
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc16028032
- 003
- CZ-PrNML
- 005
- 20181018100825.0
- 007
- ta
- 008
- 161005s2015 ne f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1016/j.nicl.2015.08.008 $2 doi
- 024 7_
- $a 10.1016/j.nicl.2015.08.008 $2 doi
- 035 __
- $a (PubMed)26509113
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a ne
- 100 1_
- $a Holiga, Štefan $u Max Planck Institute for Human Cognitive and Brain Sciences, Stephanstr. 1A, Leipzig 04103, Germany ; Leipzig Research Center for Civilization Diseases & Clinic for Cognitive Neurology, University of Leipzig, Liebigstr. 16, Leipzig 04103, Germany.
- 245 10
- $a Resting-state functional magnetic resonance imaging of the subthalamic microlesion and stimulation effects in Parkinson's disease: Indications of a principal role of the brainstem / $c Š. Holiga, K. Mueller, HE. Möller, D. Urgošík, E. Růžička, ML. Schroeter, R. Jech,
- 520 9_
- $a During implantation of deep-brain stimulation (DBS) electrodes in the target structure, neurosurgeons and neurologists commonly observe a "microlesion effect" (MLE), which occurs well before initiating subthalamic DBS. This phenomenon typically leads to a transitory improvement of motor symptoms of patients suffering from Parkinson's disease (PD). Mechanisms behind MLE remain poorly understood. In this work, we exploited the notion of ranking to assess spontaneous brain activity in PD patients examined by resting-state functional magnetic resonance imaging in response to penetration of DBS electrodes in the subthalamic nucleus. In particular, we employed a hypothesis-free method, eigenvector centrality (EC), to reveal motor-communication-hubs of the highest rank and their reorganization following the surgery; providing a unique opportunity to evaluate the direct impact of disrupting the PD motor circuitry in vivo without prior assumptions. Penetration of electrodes was associated with increased EC of functional connectivity in the brainstem. Changes in connectivity were quantitatively related to motor improvement, which further emphasizes the clinical importance of the functional integrity of the brainstem. Surprisingly, MLE and DBS were associated with anatomically different EC maps despite their similar clinical benefit on motor functions. The DBS solely caused an increase in connectivity of the left premotor region suggesting separate pathophysiological mechanisms of both interventions. While the DBS acts at the cortical level suggesting compensatory activation of less affected motor regions, the MLE affects more fundamental circuitry as the dysfunctional brainstem predominates in the beginning of PD. These findings invigorate the overlooked brainstem perspective in the understanding of PD and support the current trend towards its early diagnosis.
- 650 _2
- $a dospělí $7 D000328
- 650 _2
- $a mapování mozku $7 D001931
- 650 _2
- $a mozkový kmen $x krevní zásobení $x fyziologie $7 D001933
- 650 _2
- $a hluboká mozková stimulace $x škodlivé účinky $7 D046690
- 650 _2
- $a echoplanární zobrazování $7 D017352
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a počítačové zpracování obrazu $7 D007091
- 650 12
- $a magnetická rezonanční tomografie $7 D008279
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a lidé středního věku $7 D008875
- 650 _2
- $a kyslík $x krev $7 D010100
- 650 12
- $a Parkinsonova nemoc $x patologie $x patofyziologie $x terapie $7 D010300
- 650 12
- $a odpočinek $7 D012146
- 650 _2
- $a stupeň závažnosti nemoci $7 D012720
- 650 _2
- $a nucleus subthalamicus $x krevní zásobení $x patologie $7 D020531
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Mueller, Karsten $u Max Planck Institute for Human Cognitive and Brain Sciences, Stephanstr. 1A, Leipzig 04103, Germany.
- 700 1_
- $a Möller, Harald E $u Max Planck Institute for Human Cognitive and Brain Sciences, Stephanstr. 1A, Leipzig 04103, Germany.
- 700 1_
- $a Urgošík, Dušan, $u Department of Stereotactic and Radiation Neurosurgery, Na Homolce Hospital, Roentgenova 2, Prague 15030, Czech Republic. $d 1958- $7 jn20010310072
- 700 1_
- $a Růžička, Evžen, $u Department of Neurology and Center of Clinical Neuroscience, First Faculty of Medicine, Charles University In Prague, Kateřinská 30, Prague 12821, Czech Republic. $d 1957- $7 jo20000074065
- 700 1_
- $a Schroeter, Matthias L $u Max Planck Institute for Human Cognitive and Brain Sciences, Stephanstr. 1A, Leipzig 04103, Germany ; Leipzig Research Center for Civilization Diseases & Clinic for Cognitive Neurology, University of Leipzig, Liebigstr. 16, Leipzig 04103, Germany.
- 700 1_
- $a Jech, Robert, $u Department of Neurology and Center of Clinical Neuroscience, First Faculty of Medicine, Charles University In Prague, Kateřinská 30, Prague 12821, Czech Republic. $d 1969- $7 xx0082225
- 773 0_
- $w MED00188130 $t NeuroImage. Clinical $x 2213-1582 $g Roč. 9, č. - (2015), s. 264-274
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/26509113 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20161005 $b ABA008
- 991 __
- $a 20181018101325 $b ABA008
- 999 __
- $a ok $b bmc $g 1166346 $s 952662
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2015 $b 9 $c - $d 264-274 $e 20150821 $i 2213-1582 $m NeuroImage. Clinical $n Neuroimage Clin $x MED00188130
- GRA __
- $a NT12282 $p MZ0
- LZP __
- $a Pubmed-20161005