Evidence map›Paper›PMID 26217171›Full record

ArticleFrontiers in neuroscience2015

Closed-loop stimulation of a delayed neural fields model of parkinsonian STN-GPe network: a theoretical and computational study.

Georgios Is Detorakis, Antoine Chaillet, Stéphane Palfi, Suhan Senova

Open access · goldAbstract read
In one paragraph

Article in Frontiers in neuroscience, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.2field-weighted citation impact, top 13% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 29 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 4 institutions in 1 country.

Georgios Is DetorakisLaboratoire des Signaux et Systèmes, CentraleSupelec Gif-sur-Yvette, France ; Faculté des Sciences, Université Paris Sud Orsay, France.
Antoine ChailletLaboratoire des Signaux et Systèmes, CentraleSupelec Gif-sur-Yvette, France ; Faculté des Sciences, Université Paris Sud Orsay, France.
Stéphane PalfiAP-HP, Hospital H. Mondor, Service de neurochirurgie Créteil, France ; Institut National de la Santé et de la Recherche Médicale, U955, Equipe 14 Créteil, France ; Faculty of Medicine, Université Paris Est Créteil, France.
Suhan SenovaAP-HP, Hospital H. Mondor, Service de neurochirurgie Créteil, France ; Institut National de la Santé et de la Recherche Médicale, U955, Equipe 14 Créteil, France ; Faculty of Medicine, Université Paris Est Créteil, France.
Assistance Publique – Hôpitaux de Paris · FRCentraleSupélec · FRUniversité Paris-Est Créteil · FRUniversité Paris-Sud · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Several disorders are related to pathological brain oscillations. In the case of Parkinson's disease, sustained low-frequency oscillations (especially in the β-band, 13-30 Hz) correlate with motor symptoms. It is still under debate whether these oscillations are the cause of parkinsonian motor symptoms. The development of techniques enabling selective disruption of these β-oscillations could contribute to the understanding of the underlying mechanisms, and could be exploited for treatments. A particularly appealing technique is Deep Brain Stimulation (DBS). With clinical electrical DBS, electrical currents are delivered at high frequency to a region made of potentially heterogeneous neurons (the subthalamic nucleus (STN) in the case of Parkinson's disease). Even more appealing is DBS with optogenetics, which is until now a preclinical method using both gene transfer and deep brain light delivery and enabling neuromodulation at the scale of one given neural network. In this work, we rely on delayed neural fields models of STN and the external Globus Pallidus (GPe) to develop, theoretically validate and test in silico a closed-loop stimulation strategy to disrupt these sustained oscillations with optogenetics. First, we rely on tools from control theory to provide theoretical conditions under which sustained oscillations can be attenuated by a closed-loop stimulation proportional to the measured activity of STN. Second, based on this theoretical framework, we show numerically that the proposed closed-loop stimulation efficiently attenuates sustained oscillations, even in the case when the photosensitization effectively affects only 50% of STN neurons. We also show through simulations that oscillations disruption can be achieved when the same light source is used for the whole STN population. We finally test the robustness of the proposed strategy to possible acquisition and processing delays, as well as parameters uncertainty.

Indexed as

closed-loop deep brain stimulationcontrol theorydelayed neural fieldsoptogeneticsParkinson's diseasestability analysisβ-oscillations

Identifiers

PMID26217171
PMCPMC4498106
OpenAlexW1598024552

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.