Evidence map›Paper›PMID 18317782›Full record

ArticleActa neuropathologica2008

Cellular distribution of vascular endothelial growth factor A (VEGFA) and B (VEGFB) and VEGF receptors 1 and 2 in focal cortical dysplasia type IIB.

Karin Boer, Dirk Troost, Wim G M Spliet, Peter C van Rijen, Jan A Gorter, Eleonora Aronica

Registry-linked trialOpen access · hybridAbstract read
In one paragraph

Article in Acta neuropathologica, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01663545 (Positron Emission Tomography Measurement of Neuroinflammation in Focal Epilepsy), which is not on this map. Cited by 35 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 2 pooled it
1.5field-weighted citation impact, top 18% 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.

NCT01663545 completednot on this mapstarted 2012, after this paper: background citation

Positron Emission Tomography Measurement of Neuroinflammation in Focal Epilepsy

TypeobservationalSponsorNational Institute of Neurological Disorders and Stroke (NINDS)Ran2012 to 2017Enrolled38ConditionsEpilepsies, Partial
3 · Its place in the literature

Who cites it

35 citing papers in PubMed, 2 syntheses or guidelines pooled it, 65 citations in OpenAlex.

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  15. Disabling VEGF-Response of Purkinje Cells by Downregulation ofInternational journal of molecular sciences · 2021
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  20. Chronic stress induced disruption of the peri-infarct neurovascular unit following experimentally induced photothrombotic stroke.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2017
    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

6 authors at 3 institutions in 1 country.

Karin BoerDepartment of (Neuro) Pathology, Academic Medical Center, University of Amsterdam, Meibergdreef 9, 1105 AZ, Amsterdam, The Netherlands.
Dirk Troost
Wim G M Spliet
Peter C van Rijen
Jan A Gorter
Eleonora Aronica
University of Amsterdam · NLUniversity Medical Center Utrecht · NLStichting Epilepsie Instellingen Nederland · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Members of the vascular endothelial growth factor (VEGF) family are key signaling proteins in the induction and regulation of angiogenesis, both during development and in pathological conditions. However, signaling mediated through VEGF family proteins and their receptors has recently been shown to have direct effects on neurons and glial cells. In the present study, we immunocytochemically investigated the expression and cellular distribution of VEGFA, VEGFB, and their associated receptors (VEGFR-1 and VEGFR-2) in focal cortical dysplasia (FCD) type IIB from patients with medically intractable epilepsy. Histologically normal temporal cortex and perilesional regions displayed neuronal immunoreactivity (IR) for VEGFA, VEGFB, and VEGF receptors (VEGFR-1 and VEGFR-2), mainly in pyramidal neurons. Weak IR was observed in blood vessels and there was no notable glial IR within the grey and white matter. In all FCD specimens, VEGFA, VEGFB, and both VEGF receptors were highly expressed in dysplastic neurons. IR in astroglial and balloon cells was observed for VEGFA and its receptors. VEGFR-1 displayed strong endothelial staining in FCD. Double-labeling also showed expression of VEGFA, VEGFB and VEGFR-1 in cells of the microglia/macrophage lineage. The neuronal expression of both VEGFA and VEGFB, together with their specific receptors in FCD, suggests autocrine/paracrine effects on dysplastic neurons. These autocrine/paracrine effects could play a role in the development of FCD, preventing the death of abnormal neuronal cells. In addition, the expression of VEGFA and its receptors in glial cells within the dysplastic cortex indicates that VEGF-mediated signaling could contribute to astroglial activation and associated inflammatory reactions.

Indexed as

AdolescentAdultAntigens, CDAntigens, Differentiation, MyelomonocyticCD68 MoleculeChildEpilepsyFemaleGlial Fibrillary Acidic ProteinHumansMaleMalformations of Cortical DevelopmentMicrotubule-Associated ProteinsNeurofilament ProteinsVascular Endothelial Growth Factor AVascular Endothelial Growth Factor BAntigens, CDAntigens, Differentiation, MyelomonocyticCD68 antigen, humanCD68 MoleculeGlial Fibrillary Acidic ProteinMAP2 protein, humanMicrotubule-Associated ProteinsNeurofilament ProteinsVascular Endothelial Growth Factor AVascular Endothelial Growth Factor BVascular Endothelial Growth Factor Receptor-1Vascular Endothelial Growth Factor Receptor-2VEGFA protein, humanVEGFB protein, human

Identifiers

PMID18317782
PMCPMC2386160
OpenAlexW1984056187

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.