Evidence map›Paper›PMID 33155106›Full record

ArticleEuropean radiology2021

Progressive multifocal leukoencephalopathy: MRI findings in HIV-infected patients are closer to rituximab- than natalizumab-associated PML.

Manel Alleg, Morgane Solis, Seyyid Baloglu, François Cotton, Philippe Kerschen, Bertrand Bourre, Guido Ahle, Jean-Pierre Pruvo, Xavier Leclerc, Patrick Vermersch and 18 more

Open access · bronzeAbstract read
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 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.0field-weighted citation impact, top 21% 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

8 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
  2. Cosmic Signs in Radiology: A Pictorial Review.Diagnostics (Basel, Switzerland) · 2025
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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

28 authors at 16 institutions in 2 countries.

Manel AllegHôpitaux Universitaires de Strasbourg, Service d'imagerie 2, Hôpital de Hautepierre, Strasbourg, France. Manel.alleg@gmail.com.ORCID http://orcid.org/0000-0002-8824-5349
Morgane SolisHôpitaux universitaires de Strasbourg, Laboratoire de Virologie Médicale, Strasbourg, France.
Seyyid BalogluHôpitaux Universitaires de Strasbourg, Service d'imagerie 2, Hôpital de Hautepierre, Strasbourg, France.
François CottonMRI center, Centre Hospitalier Lyon Sud, Hospices Civils de Lyon,, Lyon, France.
Philippe KerschenCentre hospitalier de Luxembourg, Luxembourg City, Luxembourg.
Bertrand BourreRouen University Hospital, F-76000, Rouen, France.
Guido AhleService de Neurologie, Hôpitaux Civils de Colmar, Colmar, France.ORCID http://orcid.org/0000-0002-0877-2289
Jean-Pierre PruvoDepartment of Neuroradiology, University of Lille, Inserm UMR-S 1172, CHU Lille, Lille, France.
Xavier LeclercDepartment of Neuroradiology, University of Lille, Inserm UMR-S 1172, CHU Lille, Lille, France.
Patrick VermerschUniv-Lille, Inserm UMR 1172, CHU Lille, FHU Imminent, Lille, France.
Caroline PapeixDepartment of Neurology, CRC-SEP, Pitié-Salpêtrière Hospital, APHP, Paris, France.
Élisabeth MaillartDepartment of Neurology, CRC-SEP, Pitié-Salpêtrière Hospital, APHP, Paris, France.
Caroline HouillierAPHP, Sorbonne Université, IHU, ICM, Service de Neurologie 2-Mazarin, Groupe Hospitalier Pitié-Salpêtrière, Paris, France.
Cécile Moluçon ChabrotCHU de Clermont Ferrand, Clermont Ferrand, France.
Béatrice ClaiseCHU de Clermont Ferrand, Clermont Ferrand, France.
Sandra MalakService d'hématologie, Institut Curie-Saint-Cloud, Saint-Cloud, France.
Guillaume Martin-BlondelService des Maladies Infectieuses et Tropicales, CHU de Toulouse, Toulouse, France.
Fabrice BonnevilleService de Neuroradiologie, CHU de Toulouse, Toulouse, France.
Alexis CaulierHématologie Clinique, CHU Amiens-Picardie, Amiens, France.
Jean-Pierre MarolleauHématologie Clinique, CHU Amiens-Picardie, Amiens, France.
Jérôme Tamburini BonnefoyHôpital Cochin Paris, Paris, France.
Philippe AgapeInstitut de Cancérologie de l'Ouest , Saint-Herblain, Nantes, France.
Céline KennelCHU de Limoges, Limoges, France.
Xavier RousselCHU de Besançon, Besançon, France.
Adrien ChauchetCHU de Besançon, Besançon, France.
Jérôme De SezeService de Neurologie, Hôpitaux Universitaires de Strasbourg Hôpital de Hautepierre, Strasbourg, France.
Samira Fafi-KremerHôpitaux universitaires de Strasbourg, Laboratoire de Virologie Médicale, Strasbourg, France.
Stéphane KremerHôpitaux Universitaires de Strasbourg, Service d'imagerie 2, Hôpital de Hautepierre, Strasbourg, France.
Hôpitaux Universitaires de Strasbourg · FRInserm · FRSorbonne Université · FRCentre Hospitalier Universitaire Amiens-Picardie · FRCentre Hospitalier Universitaire de Besançon · FRCentre Hospitalier Universitaire de Clermont-Ferrand · FRCentre National de la Recherche Scientifique · FRCentre Hospitalier de Luxembourg · LUCentre Hospitalier Universitaire de Limoges · FRCentre Hospitalier Universitaire de Toulouse · FRHôpital Cochin · FRHopitaux Civils de Colmar · FRInstitut Curie · FRInstitut de Cancérologie de l'Ouest · FRUniversité Claude Bernard Lyon 1 · FRUniversité de Rouen Normandie · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTo compare brain MRI findings in progressive multifocal leukoencephalopathy (PML) associated to rituximab and natalizumab treatments and HIV infection. MATERIALS AND

methodsIn this retrospective, multicentric study, we analyzed brain MRI exams from 72 patients diagnosed with definite PML: 32 after natalizumab treatment, 20 after rituximab treatment, and 20 HIV patients. We compared T2- or FLAIR-weighted images, diffusion-weighted images, T2*-weighted images, and contrast enhancement features, as well as lesion distribution, especially gray matter involvement.

resultsThe three PML entities affect U-fibers associated with low signal intensities on T2*-weighted sequences. Natalizumab-associated PML showed a punctuate microcystic appearance in or in the vicinity of the main PML lesions, a potential involvement of the cortex, and contrast enhancement. HIV and rituximab-associated PML showed only mild contrast enhancement, punctuate appearance, and cortical involvement. The CD4/CD8 ratio showed a trend to be higher in the natalizumab group, possibly mirroring a more efficient immune response.

conclusionImaging features of rituximab-associated PML are different from those of natalizumab-associated PML and are closer to those observed in HIV-associated PML. KEY POINTS: • Nowadays, PML is emerging as a complication of new effective therapies based on monoclonal antibodies. • Natalizumab-associated PML shows more inflammatory signs, a perivascular distribution "the milky way," and more cortex involvement than rituximab- and HIV-associated PML. • MRI differences are probably related to higher levels of immunosuppression in HIV patients and those under rituximab therapy.

Indexed as

HIV InfectionsLeukoencephalopathy, Progressive MultifocalBrainHumansMagnetic Resonance ImagingNatalizumabRetrospective StudiesRituximabNatalizumabRituximabNatalizumabProgressive multifocal leukoencephalopathyRituximab

Identifiers

PMID33155106
PMCPMC7644389
OpenAlexW3094793707

What OpenQuestion holds

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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.