Evidence map›Paper›PMID 31549200›Full record

ArticleJournal of neurology2019

Trajectories of brain remodeling in temporal lobe epilepsy.

Elisabeth Roggenhofer, Emiliano Santarnecchi, Sandrine Muller, Ferath Kherif, Roland Wiest, Margitta Seeck, Bogdan Draganski

Abstract read
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In one paragraph

Article in Journal of neurology, 2019. 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
0.3field-weighted citation impact, top 38% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
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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

7 authors at 4 institutions in 3 countries.

Elisabeth RoggenhoferLREN, Department for Clinical Neurosciences, CHUV, University of Lausanne, Mont Paisible 16, 1011, Lausanne, Switzerland.ORCID http://orcid.org/0000-0002-0519-3740
Emiliano SantarnecchiBerenson-Allen Center for Non-Invasive Brain Stimulation, Cognitive Neurology Department, Beth Israel Medical Center, Harvard Medical School, Boston, MA, USA.
Sandrine MullerLREN, Department for Clinical Neurosciences, CHUV, University of Lausanne, Mont Paisible 16, 1011, Lausanne, Switzerland.
Ferath KherifLREN, Department for Clinical Neurosciences, CHUV, University of Lausanne, Mont Paisible 16, 1011, Lausanne, Switzerland.
Roland WiestSupport Center for Advanced Neuroimaging, Institute for Diagnostic and Interventional Neuroradiology, University Hospital Inselspital, University of Bern, Bern, Switzerland.
Margitta SeeckDepartment for Clinical Neurosciences, HUG, University Hospitals and Faculty of Medicine, Geneva, Switzerland.
Bogdan DraganskiLREN, Department for Clinical Neurosciences, CHUV, University of Lausanne, Mont Paisible 16, 1011, Lausanne, Switzerland. bogdan.draganski@chuv.ch.
University of Lausanne · CHUniversity Hospital of Lausanne · CHUniversity of Bern · CHUniversity of Siena · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Temporal lobe epilepsy has been usually associated with progressive brain atrophy due to neuronal cell loss. However, recent animal models demonstrated a dual effect of epileptic seizures with initial enhancement of hippocampal neurogenesis followed by abnormal astrocyte proliferation and neurogenesis depletion in the chronic stage. Our aim was to test for the hypothesized bidirectional pattern of epilepsy-associated brain remodeling in the context of the presence and absence of mesial temporal lobe sclerosis. We acquired MRIs from a large cohort of mesial temporal lobe epilepsy patients with or without hippocampus sclerosis on radiological examination. The statistical analysis tested explicitly for common and differential brain patterns between the two patients' cohorts and healthy controls within the computational anatomy framework of voxel-based morphometry. The main effect of disease was associated with continuous hippocampus volume loss ipsilateral to the seizure onset zone in both temporal lobe epilepsy cohorts. The post hoc simple effects tests demonstrated bilateral hippocampus volume increase in the early epilepsy stages in patients without hippocampus sclerosis. Early age of onset and longer disease duration correlated with volume decrease in the ipsilateral hippocampus. Our findings of seizure-induced hippocampal remodeling are associated with specific patterns of mesial temporal lobe atrophy that are modulated by individual clinical phenotype features. Directionality of hippocampus volume changes strongly depends on the chronicity of disease. Specific anatomy differences represent a snapshot within a progressive continuum of seizure-induced structural remodeling.

Indexed as

Disease ProgressionAdultAge of OnsetAtrophyChronic DiseaseCross-Sectional StudiesEpilepsy, Temporal LobeFemaleHippocampusHumansMagnetic Resonance ImagingMaleMiddle AgedSclerosisTime FactorsYoung AdultBrain plasticityComputational anatomyHippocampusMagnetic resonance imagingMedial temporal lobeTemporal lobe epilepsyVoxel-based morphometry

Identifiers

PMID31549200
OpenAlexW2976695882

What OpenQuestion holds

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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.