MR imaging in children with transverse myelitis and acquired demyelinating syndromes.


Journal

Multiple sclerosis and related disorders
ISSN: 2211-0356
Titre abrégé: Mult Scler Relat Disord
Pays: Netherlands
ID NLM: 101580247

Informations de publication

Date de publication:
Nov 2022
Historique:
received: 13 02 2022
revised: 13 07 2022
accepted: 21 07 2022
pubmed: 8 8 2022
medline: 10 11 2022
entrez: 7 8 2022
Statut: ppublish

Résumé

Transverse myelitis (TM) occurs isolated or within other acquired demyelinating syndromes (ADS) such as neuromyelitis optica spectrum disorders (NMOSD), multiple sclerosis (MS) or myelin oligodendrocyte glycoprotein antibody associated disorders (MOGAD). To describe and compare clinical and MRI features of children with ADS presenting with TM grouped according to antibody status and diagnosis of MS and NMOSD. Children with TM, radiological involvement of the myelon, MOG and aquaporin-4 antibody status were elegible. 100 children were identified and divided into MOGAD (n=33), NMOSD (n=7), double seronegative TM (n=34), and MS (n=26). MOGAD children had mainly acute disseminated encephalomyelitis + TM/ longitudinally extensive TM (LETM) (42%) or isolated LETM (30%). In MOGAD, LETM was present in more than half of all children (55%) with predominant involvement of only the grey matter (73%). Leptomeningeal enhancement was highly predictive of MOGAD (16/30; p=0.003). In MS patients spinal MRI showed single (50%) or multiple short lesions (46%) with involvement of grey and white matter (68%). Double seronegative children presented with LETM (74%) and brain lesions were less frequent compared to the other groups (30%). Children with ADS presenting with TM reveal important radiological differences such as LETM with predominant involvement of spinal grey matter and leptomeningeal enhancement in MOGAD.

Sections du résumé

BACKGROUND BACKGROUND
Transverse myelitis (TM) occurs isolated or within other acquired demyelinating syndromes (ADS) such as neuromyelitis optica spectrum disorders (NMOSD), multiple sclerosis (MS) or myelin oligodendrocyte glycoprotein antibody associated disorders (MOGAD).
OBJECTIVE OBJECTIVE
To describe and compare clinical and MRI features of children with ADS presenting with TM grouped according to antibody status and diagnosis of MS and NMOSD.
PATIENTS AND METHODS METHODS
Children with TM, radiological involvement of the myelon, MOG and aquaporin-4 antibody status were elegible.
RESULTS RESULTS
100 children were identified and divided into MOGAD (n=33), NMOSD (n=7), double seronegative TM (n=34), and MS (n=26). MOGAD children had mainly acute disseminated encephalomyelitis + TM/ longitudinally extensive TM (LETM) (42%) or isolated LETM (30%). In MOGAD, LETM was present in more than half of all children (55%) with predominant involvement of only the grey matter (73%). Leptomeningeal enhancement was highly predictive of MOGAD (16/30; p=0.003). In MS patients spinal MRI showed single (50%) or multiple short lesions (46%) with involvement of grey and white matter (68%). Double seronegative children presented with LETM (74%) and brain lesions were less frequent compared to the other groups (30%).
CONCLUSION CONCLUSIONS
Children with ADS presenting with TM reveal important radiological differences such as LETM with predominant involvement of spinal grey matter and leptomeningeal enhancement in MOGAD.

Identifiants

pubmed: 35933757
pii: S2211-0348(22)00576-4
doi: 10.1016/j.msard.2022.104068
pii:
doi:

Substances chimiques

Myelin-Oligodendrocyte Glycoprotein 0
Aquaporin 4 0
Autoantibodies 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

104068

Investigateurs

Nina Barišić (N)
Bettina Behring (B)
Steffen Berweck (S)
Markus Blankenburg (M)
Astrid Blaschek (A)
Christoph Conrad (C)
Katharina Diepold (K)
Matthias Eckenweiler (M)
Astrid Eisenkölbl (A)
Walid Fazeli (W)
Tobias Geis (T)
Annette Hackenberg (A)
Katharina Harms (K)
Andrea Klein (A)
Johannes Koch (J)
Barbara Kornek (B)
Margherita Nosadini (M)
Daniela Pohl (D)
Martin Pritsch (M)
Michela Salandin (M)
Torsten Sandrieser (T)
Stefano Sartori (S)
Johannes Stoffels (J)
Gert Wiegand (G)

Informations de copyright

Copyright © 2022 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest IN, RC, EW, ABe, KS, CTh, ADM, MSch, SL, AWP, NB, BB, SB, MBl, ABl, CC, KD, ME, AE, WF, TG, AH, KH, JK, BK, MN, DP, MP, MSa, TS, SS, JS, GW report no conflict of interest. Michael Karenfort served as consultant for Novartis. Christian Lechner has received compensation for consulting services from Roche. Matthias Baumann has received compensation for consulting services from Sanofi. Markus Reindl was supported by a research support from Euroimmun and Roche. The University Hospital and Medical University of Innsbruck (Austria, employer of Dr. Reindl) receive payments for antibody assays (MOG-, AQP4-, and other autoantibodies) and for MOG-and AQP4-antibody validation experiments organised by Euroimmun (Lübeck, Germany). Kevin Rostásy served as a consultant for the PARADIGM-Study/Novartis without payment and received honoraria for lectures given for MERCK. Andrea Klein did advisory activities for Novartis Gene Therapies, Biogen, Pfizer, Roche, Sarepta and Santhera and received speakers honoraria from Biogen, Roche, Sarepta and Santhera.

Auteurs

Ines El Naggar (I)

Department of Pediatric Neurology, Children´s Hospital Datteln, University Witten/Herdecke, Datteln, Germany.

Robert Cleaveland (R)

Department of Pediatric Radiology, Children´s Hospital Datteln, University Witten/Herdecke, Datteln, Germany.

Eva-Maria Wendel (EM)

Division of Pediatric Neurology, Department of Pediatrics, Olgahospital, Stuttgart, Germany.

Annikki Bertolini (A)

Department of Pediatric Neurology, Children´s Hospital Datteln, University Witten/Herdecke, Datteln, Germany.

Kathrin Schanda (K)

Medical University Innsbruck, Innsbruck, Austria.

Michael Karenfort (M)

Clinic of General Pediatrics, Neonatology and Pediatric Cardiology, Düsseldorf University Hospital, Heinrich-Heine-University, Düsseldorf, Germany.

Charlotte Thiels (C)

Division of Pediatric Neurology, Clinic of Pediatrics, St. Josef-Hospital, Ruhr-University Bochum, Bochum, Germany.

Adela Della Marina (A)

Department of Pediatric Neurology, Centre for Neuromuscular Disorders, Centre for Translational Neuro- und Behavioral Sciences, University Duisburg-Essen, Essen, Germany.

Mareike Schimmel (M)

Division of Pediatric Neurology, Clinic of Pediatrics, Augsburg University Hospital, University of Augsburg, Augsburg, Germany.

Steffen Leiz (S)

Division of Pediatric Neurology, Clinic of Pediatrics, Klinikum Dritter Orden, München, Germany.

Christian Lechner (C)

Division of Pediatric Neurology, Department of Pediatrics I, Medical University of Innsbruck, Innsbruck, Austria.

Matthias Baumann (M)

Division of Pediatric Neurology, Department of Pediatrics I, Medical University of Innsbruck, Innsbruck, Austria.

Markus Reindl (M)

Medical University Innsbruck, Innsbruck, Austria.

Andreas Wegener-Panzer (A)

Department of Pediatric Radiology, Children´s Hospital Datteln, University Witten/Herdecke, Datteln, Germany.

Kevin Rostásy (K)

Department of Pediatric Neurology, Children´s Hospital Datteln, University Witten/Herdecke, Datteln, Germany. Electronic address: k.rostasy@kinderklinik-datteln.de.

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