Evidence map›Paper›PMID 33221837›Full record

ArticleBrain : a journal of neurology2021

Dendritic pathology, spine loss and synaptic reorganization in human cortex from epilepsy patients.

Laura Rossini, Dalia De Santis, Roberta Rosa Mauceri, Chiara Tesoriero, Marina Bentivoglio, Emanuela Maderna, Antonio Maiorana, Francesco Deleo, Marco de Curtis, Giovanni Tringali and 6 more

Open access · bronzeAbstract read
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In one paragraph

Article in Brain : a journal of neurology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
5.1field-weighted citation impact, top 3% 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

55 citing papers in PubMed, 79 citations in OpenAlex.

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  10. Carvone derived cannabidiol enantiomers as novel anticonvulsants.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2025
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  16. Ablation of dysmorphic neurons is a safe and effective treatment for focal cortical dysplasia II.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 4 institutions in 1 country.

Laura RossiniEpilepsy Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milano, Italy.
Dalia De SantisEpilepsy Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milano, Italy.
Roberta Rosa MauceriEpilepsy Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milano, Italy.
Chiara TesorieroDepartment of Neurosciences, Biomedicine and Movement Sciences, University of Verona, Italy.
Marina BentivoglioDepartment of Neurosciences, Biomedicine and Movement Sciences, University of Verona, Italy.
Emanuela MadernaDivision of Neurology V and Neuropathology, Fondazione IRCCS, Istituto Neurologico Carlo Besta, Milano, Italy.
Antonio MaioranaInstitute of Pathology, Department of Medical and Surgical Sciences, University of Modena and Reggio Emilia, Modena, Italy.
Francesco DeleoEpilepsy Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milano, Italy.
Marco de CurtisEpilepsy Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milano, Italy.
Giovanni TringaliNeurosurgery Unit, Fondazione IRCCS, Istituto Neurologico Carlo Besta, Milano, Italy.
Massimo Cossu"Claudio Munari" Epilepsy Surgery Center, GOM Niguarda, Milano, Italy.
Gemma Tumminelli"Claudio Munari" Epilepsy Surgery Center, GOM Niguarda, Milano, Italy.
Manuela BramerioDepartment of Pathology, GOM Niguarda, Milano, Italy.
Roberto SpreaficoEpilepsy Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milano, Italy.
Laura Tassi"Claudio Munari" Epilepsy Surgery Center, GOM Niguarda, Milano, Italy.
Rita GarbelliEpilepsy Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milano, Italy.
Fondazione IRCCS Istituto Neurologico Carlo Besta · ITUniversity of Verona · ITAzienda Socio Sanitaria Territoriale Grande Ospedale Metropolitano Niguarda · ITUniversity of Modena and Reggio Emilia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neuronal dendritic arborizations and dendritic spines are crucial for a normal synaptic transmission and may be critically involved in the pathophysiology of epilepsy. Alterations in dendritic morphology and spine loss mainly in hippocampal neurons have been reported both in epilepsy animal models and in human brain tissues from patients with epilepsy. However, it is still unclear whether these dendritic abnormalities relate to the cause of epilepsy or are generated by seizure recurrence. We investigated fine neuronal structures at the level of dendritic and spine organization using Golgi impregnation, and analysed synaptic networks with immunohistochemical markers of glutamatergic (vGLUT1) and GABAergic (vGAT) axon terminals in human cerebral cortices derived from epilepsy surgery. Specimens were obtained from 28 patients with different neuropathologically defined aetiologies: type Ia and type II focal cortical dysplasia, cryptogenic (no lesion) and temporal lobe epilepsy with hippocampal sclerosis. Autoptic tissues were used for comparison. Three-dimensional reconstructions of Golgi-impregnated neurons revealed severe dendritic reshaping and spine alteration in the core of the type II focal cortical dysplasia. Dysmorphic neurons showed increased dendritic complexity, reduction of dendritic spines and occasional filopodia-like protrusions emerging from the soma. Surprisingly, the intermingled normal-looking pyramidal neurons also showed severe spine loss and simplified dendritic arborization. No changes were observed outside the dysplasia (perilesional tissue) or in neocortical postsurgical tissue obtained in the other patient groups. Immunoreactivities of vGLUT1 and vGAT showed synaptic reorganization in the core of type II dysplasia characterized by the presence of abnormal perisomatic baskets around dysmorphic neurons, in particular those with filopodia-like protrusions, and changes in vGLUT1/vGAT expression. Ultrastructural data in type II dysplasia highlighted the presence of altered neuropil engulfed by glial processes. Our data indicate that the fine morphological aspect of neurons and dendritic spines are normal in epileptogenic neocortex, with the exception of type II dysplastic lesions. The findings suggest that the mechanisms leading to this severe form of cortical malformation interfere with the normal dendritic arborization and synaptic network organization. The data argue against the concept that long-lasting epilepsy and seizure recurrence per se unavoidably produce a dendritic pathology.

Indexed as

AdolescentAdultCerebral CortexChild, PreschoolDendritesDendritic SpinesEpilepsyHumansInfantMicroscopy, ElectronMiddle AgedSynapsesVesicular Glutamate Transport Protein 1Vesicular Inhibitory Amino Acid Transport ProteinsYoung AdultSLC17A7 protein, humanSLC32A1 protein, humanVesicular Glutamate Transport Protein 1Vesicular Inhibitory Amino Acid Transport Proteinsdendritic spinesfocal cortical dysplasiafocal drug-resistant epilepsyGolgi impregnationhuman tissue

Identifiers

PMID33221837
OpenAlexW3107380014

What OpenQuestion holds

Textmetadata
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.