Evidence map›Paper›PMID 33259483›Full record

ArticlePLoS computational biology2020

Neural diffusivity and pre-emptive epileptic seizure intervention.

Erik D Fagerholm, Chayanin Tangwiriyasakul, Karl J Friston, Inês R Violante, Steven Williams, David W Carmichael, Suejen Perani, Federico E Turkheimer, Rosalyn J Moran, Robert Leech and 1 more

Abstract read
In one paragraph

Article in PLoS computational biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Erik D FagerholmDepartment of Neuroimaging, King's College London, London, United Kingdom.ORCID 0000-0003-2973-1395
Chayanin TangwiriyasakulDepartment of Basic and Clinical Neuroscience, King's College London, London, United Kingdom.ORCID 0000-0001-5134-0767
Karl J FristonWellcome Centre for Human Neuroimaging, University College London, London, United Kingdom.ORCID 0000-0001-7984-8909
Inês R ViolanteSchool of Psychology, University of Surrey, Guildford, United Kingdom.
Steven WilliamsDepartment of Neuroimaging, King's College London, London, United Kingdom.ORCID 0000-0003-4299-1941
David W CarmichaelSchool of Biomedical Engineering & Imaging Sciences, King's College London, London, United Kingdom.
Suejen PeraniDepartment of Basic and Clinical Neuroscience, King's College London, London, United Kingdom.
Federico E TurkheimerDepartment of Neuroimaging, King's College London, London, United Kingdom.ORCID 0000-0002-3766-3815
Rosalyn J MoranDepartment of Neuroimaging, King's College London, London, United Kingdom.
Robert LeechDepartment of Neuroimaging, King's College London, London, United Kingdom.ORCID 0000-0002-5801-6318
Mark P RichardsonDepartment of Basic and Clinical Neuroscience, King's College London, London, United Kingdom.ORCID 0000-0001-8925-3140

Funding

Biotechnology and Biological Sciences Research Council BB/S008314/1Department of HealthMedical Research Council MR/N026063/1Medical Research Council MR/R005370/1Wellcome Trust 088130/Z/09/ZWellcome Trust 103045/Z/13/ZWellcome Trust 203148/Z/16/Z
6 · The paper itself

Abstract

The propagation of epileptic seizure activity in the brain is a widespread pathophysiology that, in principle, should yield to intervention techniques guided by mathematical models of neuronal ensemble dynamics. During a seizure, neural activity will deviate from its current dynamical regime to one in which there are significant signal fluctuations. In silico treatments of neural activity are an important tool for the understanding of how the healthy brain can maintain stability, as well as of how pathology can lead to seizures. The hope is that, contained within the mathematical foundations of such treatments, there lie potential strategies for mitigating instabilities, e.g. via external stimulation. Here, we demonstrate that the dynamic causal modelling neuronal state equation generalises to a Fokker-Planck formalism if one extends the framework to model the ways in which activity propagates along the structural connections of neural systems. Using the Jacobian of this generalised state equation, we show that an initially unstable system can be rendered stable via a reduction in diffusivity-i.e., by lowering the rate at which neuronal fluctuations disperse to neighbouring regions. We show, for neural systems prone to epileptic seizures, that such a reduction in diffusivity can be achieved via external stimulation. Specifically, we show that this stimulation should be applied in such a way as to temporarily mirror the activity profile of a pathological region in its functionally connected areas. This counter-intuitive method is intended to be used pre-emptively-i.e., in order to mitigate the effects of the seizure, or ideally even prevent it from occurring in the first place. We offer proof of principle using simulations based on functional neuroimaging data collected from patients with idiopathic generalised epilepsy, in which we successfully suppress pathological activity in a distinct sub-network prior to seizure onset. Our hope is that this technique can form the basis for future real-time monitoring and intervention devices that are capable of treating epilepsy in a non-invasive manner.

Indexed as

BrainCase-Control StudiesElectroencephalographyEpilepsy, GeneralizedHumansMagnetic Resonance ImagingModels, StatisticalNerve NetSeizures

Identifiers

PMID33259483
PMCPMC7732083

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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.