Evidence map›Paper›PMID 39665957›Full record

ReviewTrends in molecular medicine2025

Bursts of brain erosion: seizures and age-dependent neurological vulnerability.

Noemie Cresto, Laurent Givalois, Jerome Badaut, Alicia Janvier, Athenais Genin, Etienne Audinat, Amy L Brewster, Nicola Marchi

Abstract readReview
In one paragraph

Review in Trends in molecular medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
–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

5 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. 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

8 authors.

Noemie CrestoInstitute of Functional Genomics, University of Montpellier, CNRS, INSERM, Montpellier, France.
Laurent GivaloisInstitute of Functional Genomics, University of Montpellier, CNRS, INSERM, Montpellier, France; Laval University, Faculty of Medicine, Department of Psychiatry and Neurosciences, Québec, Canada.
Jerome BadautCentre d'Etudes Biologiques de Chizé (CEBC), UMR 7372 CNRS - La Rochelle Université, 17031 La Rochelle, France.
Alicia JanvierInstitute of Functional Genomics, University of Montpellier, CNRS, INSERM, Montpellier, France.
Athenais GeninInstitute of Functional Genomics, University of Montpellier, CNRS, INSERM, Montpellier, France.
Etienne AudinatInstitute of Functional Genomics, University of Montpellier, CNRS, INSERM, Montpellier, France.
Amy L BrewsterDepartment of Biological Sciences, Dedman College of Humanities and Sciences, Southern Methodist University, Dallas, TX, USA. Electronic address: albrewster@smu.edu.
Nicola MarchiInstitute of Functional Genomics, University of Montpellier, CNRS, INSERM, Montpellier, France. Electronic address: nicola.marchi@igf.cnrs.fr.

Funding

A role for the complement system in seizure induced neuronal and dendritic injuryR01NS096234 · NINDS · SOUTHERN METHODIST UNIVERSITY · PI BREWSTER, AMY L. · 2019 to 2022
$1.3M
A role for the complement system in seizure induced neuronal and dendritic injuryR56NS096234 · NINDS · PURDUE UNIVERSITY · PI BREWSTER, AMY L. · 2018 to 2018
$382k
NINDS NIH HHS R01 NS096234NINDS NIH HHS R56 NS096234
6 · The paper itself

Abstract

Hypersynchronous and exaggerated neuronal firing, exemplified by epileptiform activity and seizures, are disruptors of brain function across acute and chronic neuropathological conditions. Here, we focus on how seizure activity, whether as a primary symptom or a secondary comorbid event within a complex pathological setting, adversely impacts neurological trajectories. We discuss experimental and clinical evidence illustrating the participation of neurodegenerative and senescence-like adaptations. Paroxysmal neuronal events, through bidirectional causality, are linked with immune and microvascular changes, disrupting cellular homeostasis and creating a feed-forward loop that intertwines with age-related frailty to deteriorate mental health. We emphasize the clinical significance of early detection of these brain vulnerabilities through biomarkers, monitoring neurodevelopmental risks in children, and tracking neurodegenerative disease progression in aging populations.

Indexed as

AgingBrainSeizuresAnimalsBiomarkersDisease SusceptibilityHumansNeurodegenerative DiseasesNeuronsBiomarkersagingblood–brain barrierepileptiform activityfrailtyinflammationneurological comorbidities

Identifiers

PMID39665957
PMCPMC12536483

What OpenQuestion holds

Textmetadata
LicenceTDM
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.