Cited by 97Metabolism and Genetic DisordersHereditary Neurological DisordersLysosomal Storage Disorders Research

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Frequent occurrence of cerebral demyelination in adrenomyeloneuropathy

Abstract

Objective To study the frequency of additional cerebral demyelination in Dutch patients with adrenomyeloneuropathy (AMN). Methods Consecutive patients with AMN from the Dutch X-linked adrenoleukodystrophy cohort without cerebral demyelination on MRI at inclusion, seen between January 1, 1992, and January 1, 1999, were included. Primary endpoints were brain involvement, death, or the end of follow-up on January 1, 2011. Three levels of certainty were used for cerebral demyelination: (1) signs and symptoms reported by relatives and treating physicians, confirmed by brain MRI; if follow-up MRIs were not available, (2) based upon information from treating physicians and relatives, and (3) based upon information obtained from relatives only. Results were compared with a study published in 2001, in which 13/68 (19.1%) patients with AMN developed cerebral demyelination in 9.5 ± 5.5 years. Differences of the proportions of patients with cerebral demyelination and their 95% confidence intervals (CIs) were calculated. Results Of 27 patients with AMN, 17 (63%) developed cerebral demyelination 10.2 ± 6.9 years after onset of myelo(neuro)pathy. Mean survival was 3.4 ± 2.9 years. Brain involvement was higher in Dutch patients with AMN (difference 44%, 95% CI 0.23-0.64). Conclusions Cerebral demyelination in AMN may be more frequent than previously reported. Survival is as poor as in childhood cerebral adrenoleukodystrophy. Therapies that can halt cerebral demyelination in these patients ar…

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References 11 · Cited by 97

Research works printed but not linked: 8

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Metadata

Authors
de Beer, M., Engelen, M., & van Geel, B. M.
Affiliations
Amsterdam UMC Location University of Amsterdam (NL)
Venue
Neurology
Published
2014-12-09
Volume
83
Issue
24
Pages
2227-2231
ISSN
  • 0028-3878 (ISSN-L)
  • 1526-632X
OpenAlex
W2076153637
Cited by
97
References
11
Citations by year
2026: 10 · 2025: 5 · 2024: 18 · 2023: 4 · 2022: 10 · 2021: 9 · 2020: 9 · 2019: 8 · 2018: 5 · 2017: 4 · 2016: 10 · 2015: 4
FWCI
4.13
Type
journal article
Language
en
Open access
closed
Locations
  • Neurology (publishedVersion)
  • PubMed (publishedVersion)
  • Pure Amsterdam UMC (publishedVersion)
  • Data Archiving and Networked Services (DANS) (submittedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Clinical Biochemistry › Metabolism and Genetic Disorders
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Hereditary Neurological Disorders
  • Health Sciences › Medicine › Genetics (clinical) › Lysosomal Storage Disorders Research
Keywords
adrenomyeloneuropathy, brain demyelination, adrenoleukodystrophy, X-linked adrenoleukodystrophy, brain involvement, survival, disease progression, childhood cerebral adrenoleukodystrophy
MeSH terms
Adrenoleukodystrophy, Adult, Brain, Brain Diseases, Demyelinating Diseases, Follow-Up Studies, Humans, Magnetic Resonance Imaging, Male, Middle Aged, Netherlands, Cohort Studies, Young Adult

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