4H Leukodystrophy: A Brain Magnetic Resonance Imaging Scoring System

Author:

Vrij-van den Bos Suzanne1,Hol Janna1,La Piana Roberta23,Harting Inga4,Vanderver Adeline5,Barkhof Frederik67,Cayami Ferdy18,van Wieringen Wessel9,Pouwels Petra1011,van der Knaap Marjo11112,Bernard Geneviève31314,Wolf Nicole111

Affiliation:

1. Department of Child Neurology, VU University Medical Center, Amsterdam, The Netherlands

2. Laboratory of Neurogenetics of Motion and Department of Neuroradiology, Montreal Neurological Institute and Hospital, McGill University, Montreal, Canada

3. Department of Neurology and Neurosurgery, and Pediatrics, McGill University, Montreal, Canada

4. Department of Neuroradiology, University Hospital Heidelberg, Heidelberg, Germany

5. Department of Neurology, Children's National Medical Center, Washington DC and George Washington University School of Medicine, Washington, Dist. of Columbia, United States

6. Department of Radiology, VU University Medical Center, Amsterdam, The Netherlands

7. Institute of Neurology and Health Care Engineering, University College London, London, United Kingdom

8. Department of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands

9. Department of Clinical Epidemiology and Biostatistics, VU University Medical Center and Department of Mathematics, VU University, Amsterdam, The Netherlands

10. Department of Physics and Medical Technology, VU University Medical Center, Amsterdam, The Netherlands

11. Amsterdam Neuroscience, Amsterdam, The Netherlands

12. Department of Functional Genomics, VU University, Amsterdam, The Netherlands

13. Department of Medical Genetics, McGill University Health Center, Montreal Children's Hospital, Montreal, Canada

14. Child Health and Human Development Program, Research Institute of the McGill University Health Center, Montreal, Canada

Abstract

4H (hypomyelination, hypodontia and hypogonadotropic hypogonadism) leukodystrophy (4H) is an autosomal recessive hypomyelinating white matter (WM) disorder with neurologic, dental, and endocrine abnormalities. The aim of this study was to develop and validate a magnetic resonance imaging (MRI) scoring system for 4H. A scoring system (0–54) was developed to quantify hypomyelination and atrophy of different brain regions. Pons diameter and bicaudate ratio were included as measures of cerebral and brainstem atrophy, and reference values were determined using controls. Five independent raters completed the scoring system in 40 brain MRI scans collected from 36 patients with genetically proven 4H. Interrater reliability (IRR) and correlations between MRI scores, age, gross motor function, gender, and mutated gene were assessed. IRR for total MRI severity was found to be excellent (intraclass correlation coefficient: 0.87; 95% confidence interval: 0.80–0.92) but varied between different items with some (e.g., myelination of the cerebellar WM) showing poor IRR. Atrophy increased with age in contrast to hypomyelination scores. MRI scores (global, hypomyelination, and atrophy scores) significantly correlated with clinical handicap (p < 0.01 for all three items) and differed between the different genotypes. Our 4H MRI scoring system reliably quantifies hypomyelination and atrophy in patients with 4H, and MRI scores reflect clinical disease severity.

Publisher

Georg Thieme Verlag KG

Subject

Neurology (clinical),General Medicine,Pediatrics, Perinatology and Child Health

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