Pathological basis of diffusely abnormal white matter: insights from magnetic resonance imaging and histology
Abstract
Background The pathological basis of diffusely abnormal white matter (DAWM) in multiple sclerosis (MS) has not been elucidated in detail, but may be an important element in disability and clinical progression. Methods Fifty-three subjects with MS were examined with T₁, multi-echo T₂ and magnetization transfer (MT). Twenty-three samples of formalin-fixed MS brain tissue were examined with multi-echo T₂ and subsequently stained for myelin phospholipids using luxol fast blue, for axons using Bielschowsky, immunohistochemically for the myelin proteins myelin basic protein (MBP) and 2',3'-cyclic nucleotide 3' phosphohydrolase (CNP) and for astrocytes using glial fibrillary acidic protein (GFAP). Regions of interest in DAWM were compared with normal appearing white matter. Results Fourteen of 53 subjects with MS in the in vivo study showed the presence of DAWM. Subjects with DAWM were found to have a significantly lower Expanded Disability Status Scale (EDSS) and shorter disease duration (DD) when compared with subjects without DAWM (EDSS: 1.5 versus 3.0, p = 0.031; DD: 5.4 versus 10.3 years, p = 0.045). DAWM in vivo had reduced myelin water and MT ratio, and increased T₂ and water content. Histological analysis suggests DAWM, which shows a reduction of the myelin water fraction, is characterized by selective reduction of myelin phospholipids, but with a relative preservation of myelin proteins and axons. Conclusions These findings suggest that the primary abnormality in DAWM is a…
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In papers that used multiple histological methods, validation results were not always the same for different histological markers.
“In the few papers that used multiple histological methods, validation results were not always the same for the different histological markers used”
From Can MRI measure myelin? Systematic review, qualitative assessment, and meta-analysis of studies validating microstructural imaging with myelin histology (2021) · cites this paper as Laule, Vavasour, Leung, Li, Kozlowski, Traboulsee, Oger, Mackay, Moore, 2011
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Lazari, A., & Lipp, I. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2021.117744 · Cited by 176 · see citing works
- Authors
- Laule, C., Vavasour, I. M., Leung, E., Li, D. K., Kozlowski, P., Traboulsee, A. L., Oger, J., MacKay, A. L., & Moore, G. W.
- Affiliations
- University of British Columbia (CA)
- Radiology, University of British Columbia, Vancouver, Canada.
- Venue
- Multiple Sclerosis Journal
- Publisher
- SAGE Publications
- Published
- 2010-10-21
- Volume
- 17
- Issue
- 2
- Pages
- 144-150
- ISSN
- 1352-4585 (ISSN-L)
- 1477-0970
- OpenAlex
- W1990917514
- Cited by
- 77
- References
- 0
- Citations by year
- 2025: 5 · 2024: 9 · 2023: 6 · 2022: 1 · 2021: 8 · 2020: 11 · 2019: 2 · 2018: 2 · 2017: 6 · 2016: 5 · 2015: 3 · 2014: 6 · 2013: 5 · 2012: 4
- FWCI
- 2.38
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Multiple Sclerosis Journal (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Pathology and Forensic Medicine › Multiple Sclerosis Research Studies
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Advanced Neuroimaging Techniques and Applications
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Advanced MRI Techniques and Applications
- Keywords
- multiple sclerosis, myelin water fraction, magnetization transfer, myelin basic protein, cyclic nucleotide 3'-phosphohydrolase, glial fibrillary acidic protein, astrocytes, axons, disability progression, disease duration, normal-appearing white matter
- MeSH terms
- Adult, Aged, Astrocytes, Axons, Brain, Brain Chemistry, Disability Evaluation, Myelin Basic Protein, Female, Glial Fibrillary Acidic Protein, Humans, Immunohistochemistry, Magnetic Resonance Imaging, Male, Middle Aged, Nerve Tissue Proteins, Phosphoric Diester Hydrolases, Phospholipids, Predictive Value of Tests, Staining and Labeling, Transcription Factors, Water, Multiple Sclerosis, Chronic Progressive, Multiple Sclerosis, Relapsing-Remitting, Young Adult, 2',3'-Cyclic Nucleotide 3'-Phosphodiesterase
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