Evidence map›Paper›PMID 32144956›Full record

ArticleThe Journal of physiology2020

Spike-wave discharges in absence epilepsy: segregation of electrographic components reveals distinct pathways of seizure activity.

Jonas Terlau, Jenq-Wei Yang, Zeinab Khastkhodaei, Thomas Seidenbecher, Heiko J Luhmann, Hans-Christian Pape, Annika Lüttjohann

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In one paragraph

Article in The Journal of physiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

17 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. The Reciprocal Relationship between Sleep and Epilepsy.Journal of personalized medicine · 2024
    Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Paradoxical Hyperexcitability in Disorders of Neurodevelopment.Frontiers in molecular neuroscience · 2022
    Review
  13. Article
  14. Review
  15. Review
  16. Article
  17. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Jonas TerlauInstitute of Physiology I, Westfälische Wilhelms University Münster, Münster, Germany.
Jenq-Wei YangInstitute of Physiology, University Medical Center of the Johannes Gutenberg University Mainz, Mainz, Germany.
Zeinab KhastkhodaeiInstitute of Physiology, University Medical Center of the Johannes Gutenberg University Mainz, Mainz, Germany.
Thomas SeidenbecherInstitute of Physiology I, Westfälische Wilhelms University Münster, Münster, Germany.
Heiko J LuhmannInstitute of Physiology, University Medical Center of the Johannes Gutenberg University Mainz, Mainz, Germany.
Hans-Christian PapeInstitute of Physiology I, Westfälische Wilhelms University Münster, Münster, Germany.ORCID 0000-0001-6874-8224
Annika LüttjohannInstitute of Physiology I, Westfälische Wilhelms University Münster, Münster, Germany.ORCID 0000-0002-9248-1264
University of Münster · DEJohannes Gutenberg University Mainz · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

key pointsThe major electrophysiological hallmarks of absence seizures are spike and wave discharges (SWDs), consisting of a sharp spike component and a slow wave component. In a widely accepted scheme, these components are functionally coupled and reflect an iterative progression of neuronal excitation during the spike and post-excitatory silence during the wave. In a genetic rat model of absence epilepsy, local pharmacological inhibition of the centromedian thalamus (CM) selectively suppressed the spike component, leaving self-contained waves in epidural recordings. Thalamic inputs induced activity in cortical microcircuits underlying the spike component, while intracortical oscillations generated the wave component. Based on these findings, we propose a model in which oscillatory waves provide adequate time windows for integration of thalamocortical inputs and feedback responses during generation of a synchronized SWD. ABSTRACT: Spike and wave discharges (SWDs) are the electrographic hallmark of absence seizures and the major diagnostic criterion for childhood absence epilepsy (CAE). In a widely accepted scheme, the alternating sequence of spikes and waves reflects an iterative progression of neuronal excitation during the spike component and post-excitatory silence during the wave component. Here we challenge this view by showing that these two components are not necessarily coupled. In a genetic rat model of CAE, self-contained waves occurred in motor cortex in synchrony with SWDs in the somatosensory system during blockade of afferent input from the thalamus. Current-source density analyses of multi-site local field potentials (LFPs) revealed layer-specific activity, in which thalamic inputs induced a sequence of cellular-synaptic events underlying the spike component, while intracortical oscillations generated the wave component. These findings indicate novel principles of SWDs, where oscillatory cortical waves provide adequate time windows for integration of thalamocortical inputs and feedback responses during generation of seizure activity.

Indexed as

Epilepsy, AbsenceAnimalsCerebral CortexChildElectroencephalographyHumansNeuronsPatient DischargeRatsSeizuresThalamuscentromedian thalamic nucleuscurrent-source density analysisgenetic absence epilepsy modelsseizure generalizationsomatosensory cortex

Identifiers

PMID32144956
OpenAlexW3009759002

What OpenQuestion holds

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Read underepoch 390

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.