Evidence map›Paper›PMID 34003354›Full record

ArticleEuropean radiology2021

Radiogenomics of diffuse intrinsic pontine gliomas (DIPGs): correlation of histological and biological characteristics with multimodal MRI features.

Raphaël Calmon, Volodia Dangouloff-Ros, Pascale Varlet, Christophe Deroulers, Cathy Philippe, Marie-Anne Debily, David Castel, Kevin Beccaria, Thomas Blauwblomme, David Grevent and 9 more

Abstract read
PubMed Publisher
In one paragraph

Article in European radiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

16 citing papers in PubMed, 23 citations in OpenAlex.

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  6. Molecular and Pathological Features of Paediatric High-Grade Gliomas.International journal of molecular sciences · 2024
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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

19 authors at 5 institutions in 1 country.

Raphaël Calmon *Pediatric Radiology Department, AP-HP, Hôpital Universitaire Necker-Enfants Malades, 149 rue de Sèvres, F-75015, Paris, France.
Volodia Dangouloff-Ros *Pediatric Radiology Department, AP-HP, Hôpital Universitaire Necker-Enfants Malades, 149 rue de Sèvres, F-75015, Paris, France. volodia.dangouloff-ros@aphp.fr.ORCID http://orcid.org/0000-0003-1260-5886
Pascale VarletNeuropathology Department, Sainte-Anne Hospital, F-75014, Paris, France.
Christophe DeroulersUniversité Paris-Saclay, CNRS/IN2P3, IJCLab, F-91405, Orsay, France.
Cathy PhilippeUniversité Paris-Saclay, Neurospin, Institut Joliot, CEA, Gif-sur-Yvette, France.
Marie-Anne DebilyUniversité Paris-Saclay, UMR8203, CNRS, F-94805, Villejuif, France.
David CastelUniversité Paris-Saclay, UMR8203, CNRS, F-94805, Villejuif, France.
Kevin BeccariaPediatric Neurosurgery Department, AP-HP, Hôpital Universitaire Necker-Enfants Malades, F-75015, Paris, France.
Thomas BlauwblommePediatric Neurosurgery Department, AP-HP, Hôpital Universitaire Necker-Enfants Malades, F-75015, Paris, France.
David GreventPediatric Radiology Department, AP-HP, Hôpital Universitaire Necker-Enfants Malades, 149 rue de Sèvres, F-75015, Paris, France.
Raphael LevyPediatric Radiology Department, AP-HP, Hôpital Universitaire Necker-Enfants Malades, 149 rue de Sèvres, F-75015, Paris, France.
Charles-Joris RouxPediatric Radiology Department, AP-HP, Hôpital Universitaire Necker-Enfants Malades, 149 rue de Sèvres, F-75015, Paris, France.
Yvonne PurcellRadiology Department, Fondation Rothschild, F-75019, Paris, France.
Ana SaitovitchUniversité de Paris, INSERM ERL UA10, F-75015, Paris, France.
Monica ZilboviciusUniversité de Paris, INSERM ERL UA10, F-75015, Paris, France.
Christelle DufourUniversité Paris-Saclay, UMR8203, CNRS, F-94805, Villejuif, France.
Stéphanie PugetPediatric Neurosurgery Department, AP-HP, Hôpital Universitaire Necker-Enfants Malades, F-75015, Paris, France.
Jacques GrillUniversité Paris-Saclay, UMR8203, CNRS, F-94805, Villejuif, France.
Nathalie BoddaertPediatric Radiology Department, AP-HP, Hôpital Universitaire Necker-Enfants Malades, 149 rue de Sèvres, F-75015, Paris, France.
Hôpital Necker-Enfants Malades · FRCentre National de la Recherche Scientifique · FRInserm · FRCommissariat à l'Énergie Atomique et aux Énergies Alternatives · FRFondation de Rothschild · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesThe diffuse intrinsic pontine gliomas (DIPGs) are now defined by the type of histone H3 mutated at lysine 27. We aimed to correlate the multimodal MRI features of DIPGs, H3K27M mutant, with their histological and molecular characteristics.

methodsTwenty-seven treatment-naïve children with histopathologically confirmed DIPG H3K27M mutant were prospectively included. MRI performed prior to biopsy included multi-b-value diffusion-weighted imaging, ASL, and dynamic susceptibility contrast (DSC) perfusion imaging. The ADC and cerebral blood flow (CBF) and blood volume (CBV) were measured at the biopsy site. We assessed quantitative histological data, including microvascular density, nuclear density, and H3K27M-positive nuclear density. Gene expression profiling was also assessed in the samples. We compared imaging and histopathological data according to histone subgroup. We correlated MRI quantitative data with histological data and gene expression.

resultsH3.1K27M mutated tumors showed higher ADC values (median 3151 μm

conclusionsH3.1K27M mutated tumors have higher ADC and lower perfusion values than H3.3K27M ones, without direct correlation with microvascular or nuclear density. This may be due to tissular edema possibly related to gated channel activity-related gene expression. KEY POINTS: • H3.1K27M mutant DIPG had higher apparent diffusion coefficient (p = 0.003), lower α (p = 0.048), and lower relative cerebral blood volume (p = 0.02) than H3.3K27M mutant DIPG at their biopsy sites. • Biopsy samples obtained within the tumor's enhancing portion showed higher microvascular density (p = 0.03) than samples obtained outside the tumor's enhancing portion, but similar H3K27M-positive nuclear density (p = 0.84). • Relative cerebral blood volume measured at the biopsy site was significantly correlated with H3K27M-positive nuclear density (rho = 0.74, p = 0.02).

Indexed as

Brain NeoplasmsBrain Stem NeoplasmsDiffuse Intrinsic Pontine GliomaGliomaChildHistonesHumansMagnetic Resonance ImagingHistonesChildDiffuse intrinsic pontine gliomaDiffusion magnetic resonance imagingGenetic association studiesPerfusion-weighted magnetic resonance imaging

Identifiers

PMID34003354
OpenAlexW3162251348

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Registered trials

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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.