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Abstract

Background:

Paediatric multiple sclerosis (pedMS) patients at a single site were shown to have reduced brain volumes and failure of age-expected brain growth compared to healthy controls. However, the precise time of onset of brain volume loss remains unclear.

Objective:

To longitudinally study brain volumes in a multi-centre European cohort at first presentation and after 2 years.

Methods:

Brain volumes of high-resolution magnetic resonance imaging (MRI) data from 37 pedMS patients at first presentation prior to steroid therapy and at 2-year follow-up (n = 21) were compared to matched longitudinal MRI data from the NIH Paediatric MRI Data Repository.

Results:

Patients showed significantly reduced whole brain, grey and white matter and increased ventricular volumes at initial presentation and at follow-up compared to controls. Over 2 years, patients exhibited significant reduction of whole brain and white matter volumes, accompanied by increased ventricular volume. Brain volume loss at follow-up correlated with a higher number of infratentorial lesions, relapses and an increased Expanded Disability Status Scale (EDSS) score.

Conclusions:

In pedMS patients, brain volume loss is present already at first clinical presentation and accelerated over 2 years. Increased disease activity is associated with more severe brain volume loss. MRI brain volume change might serve as an outcome parameter in future prospective pedMS studies.

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Published In

Article first published online: April 4, 2019
Issue published: June 2019

Keywords

  1. Paediatric multiple sclerosis
  2. magnetic resonance volumetry
  3. brain growth
  4. disease-modifying therapies

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© The Author(s), 2019.
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History

Manuscript received: August 9, 2018
Revision received: December 4, 2018
Manuscript accepted: December 23, 2018
Published online: April 4, 2019
Issue published: June 2019
PubMed: 30945587

Authors

Affiliations

Frederik Bartels
Department of Neurology, Charité – Universitätsmedizin Berlin, Berlin, Germany/ Berlin School of Mind and Brain, Humboldt-Universität zu Berlin, Berlin, Germany
Katharina Nobis
Department of Paediatric Neurology, Children’s Hospital Datteln, Witten/Herdecke University, Datteln, Germany
Graham Cooper
Department of Neurology, Charité – Universitätsmedizin Berlin, Berlin, Germany
Eva Wendel
Department of Paediatric Neurology, Olgahospital, Stuttgart, Germany
Robert Cleaveland
Department of Paediatric Neurology, Children’s Hospital Datteln, Witten/Herdecke University, Datteln, Germany
Barbara Bajer-Kornek
Department of Neurology, Medical University of Vienna, Vienna, Austria
Astrid Blaschek
Department of Paediatric Neurology and Developmental Medicine, Dr. von Hauner Children’s Hospital, Ludwig-Maximilians-University of Munich, Munich, Germany
Mareike Schimmel
Department of Paediatric Neurology, Children’s Hospital Augsburg, Augsburg, Germany
Markus Blankenburg
Department of Paediatric Neurology, Children’s Hospital Datteln, Witten/Herdecke University, Datteln, Germany/ Department of Paediatric Neurology, Olgahospital, Stuttgart, Germany
Matthias Baumann
Division of Paediatric Neurology, Department of Paediatrics I, Medical University of Innsbruck, Innsbruck, Austria
Michael Karenfort
Department of General Paediatrics, Neonatology and Paediatric Cardiology, University Children’s Hospital, Heinrich-Heine-University, Düsseldorf, Germany
Carsten Finke
Department of Neurology, Charité – Universitätsmedizin Berlin, Berlin, Germany/ Berlin School of Mind and Brain, Humboldt-Universität zu Berlin, Berlin, Germany
Kevin Rostásy
Department of Paediatric Neurology, Children’s Hospital Datteln, Witten/Herdecke University, Datteln, Germany

Notes

Department of Paediatric Neurology, Children’s Hospital Datteln, Witten/Herdecke University, Dr. Friedrich Steiner Street 5, D-45711 Datteln, Germany. [email protected]

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