Evidence map›Paper›PMID 37797040›Full record

ArticlePLoS computational biology2023

Circadian distribution of epileptiform discharges in epilepsy: Candidate mechanisms of variability.

Isabella Marinelli, Jamie J Walker, Udaya Seneviratne, Wendyl D'Souza, Mark J Cook, Clare Anderson, Andrew P Bagshaw, Stafford L Lightman, Wessel Woldman, John R Terry

Open access · goldAbstract read
In one paragraph

Article in PLoS computational biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

8 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. BioClocks UK: driving robust cycles of discovery to impact.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2025
    Review
  7. Article
  8. Article
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

10 authors at 5 institutions in 2 countries.

Isabella MarinelliCentre for Systems Modelling and Quantitative Biomedicine, University of Birmingham, Birmingham, United Kingdom.ORCID 0000-0003-0415-4851
Jamie J WalkerEPSRC Centre for Predictive Modelling in Healthcare, University of Exeter, Exeter, United Kingdom.
Udaya SeneviratneDepartment of Neurosciences, Monash Health, Clayton, Australia.
Wendyl D'SouzaDepartment of Medicine, St. Vincent's Hospital, University of Melbourne, Melbourne, Australia.
Mark J CookDepartment of Neuroscience, St. Vincent's Hospital, University of Melbourne, Melbourne, Australia.
Clare AndersonSchool of Psychological Sciences and Turner Institute for Brain and Mental Health, Monash University, Clayton, Australia.
Andrew P BagshawCentre for Human Brain Health, University of Birmingham, Birmingham, United Kingdom.
Stafford L LightmanBristol Medical School: Translational Health Sciences, University of Bristol, Bristol, United Kingdom.
Wessel WoldmanCentre for Systems Modelling and Quantitative Biomedicine, University of Birmingham, Birmingham, United Kingdom.
John R TerryCentre for Systems Modelling and Quantitative Biomedicine, University of Birmingham, Birmingham, United Kingdom.
University of Birmingham · GBThe University of Melbourne · AUEngineering and Physical Sciences Research Council · GBMonash University · AUUniversity of Bristol · GB

Funding

Medical Research Council MR/N008936/1Medical Research Council MR/T032480/1
6 · The paper itself

Abstract

Epilepsy is a serious neurological disorder characterised by a tendency to have recurrent, spontaneous, seizures. Classically, seizures are assumed to occur at random. However, recent research has uncovered underlying rhythms both in seizures and in key signatures of epilepsy-so-called interictal epileptiform activity-with timescales that vary from hours and days through to months. Understanding the physiological mechanisms that determine these rhythmic patterns of epileptiform discharges remains an open question. Many people with epilepsy identify precipitants of their seizures, the most common of which include stress, sleep deprivation and fatigue. To quantify the impact of these physiological factors, we analysed 24-hour EEG recordings from a cohort of 107 people with idiopathic generalized epilepsy. We found two subgroups with distinct distributions of epileptiform discharges: one with highest incidence during sleep and the other during day-time. We interrogated these data using a mathematical model that describes the transitions between background and epileptiform activity in large-scale brain networks. This model was extended to include a time-dependent forcing term, where the excitability of nodes within the network could be modulated by other factors. We calibrated this forcing term using independently-collected human cortisol (the primary stress-responsive hormone characterised by circadian and ultradian patterns of secretion) data and sleep-staged EEG from healthy human participants. We found that either the dynamics of cortisol or sleep stage transition, or a combination of both, could explain most of the observed distributions of epileptiform discharges. Our findings provide conceptual evidence for the existence of underlying physiological drivers of rhythms of epileptiform discharges. These findings should motivate future research to explore these mechanisms in carefully designed experiments using animal models or people with epilepsy.

Indexed as

EpilepsyEpilepsy, GeneralizedAnimalsElectroencephalographyHumansHydrocortisoneSeizuresHydrocortisone

Identifiers

PMID37797040
PMCPMC10581478
OpenAlexW4387362626

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.