Evidence map›Paper›PMID 39138652›Full record

ArticleJournal of neurology2024

Rasmussen's encephalitis: structural, functional, and clinical correlates of contralesional epileptiform activity.

Tobias Bauer, Randi D von Wrede, Suresh Pujar, Attila Rácz, Christian Hoppe, Tobias Baumgartner, Sophia Varadkar, Nina R Held, Johannes T Reiter, Selma Enders and 17 more

Abstract read
In one paragraph

Article in Journal of neurology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

27 authors.

Tobias Bauer *Department of Neuroradiology, University Hospital Bonn, Bonn, Germany.ORCID http://orcid.org/0000-0002-0555-6214
Randi D von Wrede *Department of Epileptology, University Hospital Bonn, Bonn, Germany.
Suresh PujarDepartment of Neurology, Great Ormond Street Hospital for Children, London, UK.
Attila RáczDepartment of Epileptology, University Hospital Bonn, Bonn, Germany.
Christian HoppeDepartment of Epileptology, University Hospital Bonn, Bonn, Germany.
Tobias BaumgartnerDepartment of Epileptology, University Hospital Bonn, Bonn, Germany.
Sophia VaradkarDepartment of Neurology, Great Ormond Street Hospital for Children, London, UK.
Nina R HeldDepartment of Neuroradiology, University Hospital Bonn, Bonn, Germany.
Johannes T ReiterDepartment of Neuroradiology, University Hospital Bonn, Bonn, Germany.
Selma EndersDepartment of Epileptology, University Hospital Bonn, Bonn, Germany.
Bastian DavidDepartment of Epileptology, University Hospital Bonn, Bonn, Germany.
Conrad C PrillwitzDepartment of Epileptology, University Hospital Bonn, Bonn, Germany.
Mar BruguesSection for Translational Epilepsy Research, Department of Neuropathology, University Hospital Bonn, Bonn, Germany.
Vera C W KeilDepartment of Epileptology, University Hospital Bonn, Bonn, Germany.
Monika JeubDepartment of Epileptology, University Hospital Bonn, Bonn, Germany.
Valeri BorgerDepartment of Neurosurgery, University Hospital Bonn, Bonn, Germany.
Josemir W SanderDepartment of Clinical & Experimental Epilepsy, UCL Queen Square Institute of Neurology, London, UK.
Wolfram S KunzDepartment of Epileptology, University Hospital Bonn, Bonn, Germany.
Alexander RadbruchDepartment of Neuroradiology, University Hospital Bonn, Bonn, Germany.
Bernd WeberInstitute of Experimental Epileptology and Cognition Research, University Hospital Bonn, Bonn, Germany.
Christoph HelmstaedterDepartment of Epileptology, University Hospital Bonn, Bonn, Germany.
Hartmut VatterDepartment of Neurosurgery, University Hospital Bonn, Bonn, Germany.
Torsten BaldewegDevelopmental Neurosciences Research and Teaching Department, UCL NIHR BRC Great Ormond Street Institute of Child Health, London, UK.
Albert J BeckerSection for Translational Epilepsy Research, Department of Neuropathology, University Hospital Bonn, Bonn, Germany.
J Helen CrossDepartment of Neurology, Great Ormond Street Hospital for Children, London, UK.
Rainer SurgesDepartment of Epileptology, University Hospital Bonn, Bonn, Germany.
Theodor RüberDepartment of Neuroradiology, University Hospital Bonn, Bonn, Germany. theodor.rueber@ukbonn.de.ORCID http://orcid.org/0000-0002-6180-7671

Funding

BONFOR research commission of the Medical Faculty of the University of Bonn 2022-1A-21
6 · The paper itself

Abstract

Progressive inflammation of one hemisphere characterises Rasmussen's encephalitis (RE), but contralesional epileptiform activity has been repeatedly reported. We aimed to quantify contralesional epileptiform activity in RE and uncover its functional and structural underpinnings. We retrospectively ascertained people with RE treated between 2000 and 2018 at a tertiary centre (Centre 1) and reviewed all available EEG datasets. The temporal occurrence of preoperative contralesional epileptiform activity (interictal/ictal) was evaluated using mixed-effects logistic regression. Cases with/without contralesional epileptiform activity were compared for cognition, inflammation (ipsilesional brain biopsies), and MRI (cortical and fixel-based morphometry). EEG findings were validated in a second cohort treated at another tertiary centre (Centre 2) between 1995 and 2020. We included 127 people with RE and 687 EEG samples. Preoperatively, contralesional epileptiform activity was seen in 30/68 (44%, Centre 1) and 8/59 (14%, Centre 2). In both cohorts, this activity was associated with younger onset age (OR = 0.9; 95% CI 0.83-0.97; P = 0.006). At centre 1, contralesional epileptiform activity was associated with contralesional MRI alterations, lower intelligence (OR = 5.19; 95% CI 1.28-21.08; P = 0.021), and impaired verbal memory (OR = 10.29; 95% CI 1.97-53.85; P = 0.006). After hemispherotomy, 11/17 (65%, Centre 1) and 28/37 (76%, Centre 2) were seizure-free. Contralesional epileptiform activity was persistent postoperatively in 6/12 (50%, Centre 1) and 2/34 (6%, Centre 2). Preoperative contralesional epileptiform activity reduced the chance of postoperative seizure freedom in both cohorts (OR = 0.69; 95% CI 0.50-0.95; P = 0.029). Our findings question the concept of strict unilaterality of RE and provide the evidence of contralesional epileptiform activity as a possible EEG predictor for persisting postoperative seizures.

Indexed as

ElectroencephalographyEncephalitisMagnetic Resonance ImagingAdolescentAdultChildChild, PreschoolFemaleHumansMaleRetrospective StudiesYoung AdultEEGEpilepsyMRINeuroimmunologyNeuropsychology

Identifiers

PMID39138652
PMCPMC11446947

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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.