Voxel-based morphometry in autopsy proven PSP and CBD
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The aim of this study was to compare the patterns of grey and white matter atrophy on MRI in autopsy confirmed progressive supranuclear palsy (PSP) and corticobasal degeneration (CBD), and to determine whether the patterns vary depending on the clinical syndrome. Voxel-based morphometry was used to compare patterns of atrophy in 13 PSP and 11 CBD subjects and 24 controls. PSP and CBD subjects were also subdivided into those with a dominant dementia or extrapyramidal syndrome. PSP subjects showed brainstem atrophy with involvement of the cortex and underlying white matter. Frontoparietal grey and subcortical grey matter atrophy occurred in CBD. When subdivided, PSP subjects with an extrapyramidal syndrome had more brainstem atrophy and less cortical atrophy than CBD subjects with an extrapyramidal syndrome. PSP subjects with a dementia syndrome had more subcortical white matter atrophy than CBD subjects with a dementia syndrome. These results show regional differences between PSP and CBD that are useful in predicting the underlying pathology, and help to shed light on the in vivo distribution of regional atrophy in PSP and CBD.
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CXCR4 and EGFR demonstrated elevated transcripts within the cerebellum and deep gray nuclei, regions more affected in CBD and PSP than FTD.
“Interestingly, CXCR4 and EGFR demonstrated elevated transcripts within the cerebellum and deep gray nuclei (thalamus and globus pallidus), regions more affected in CBD and PSP than FTD [6, 22, 34].”
From Shared genetic risk between corticobasal degeneration, progressive supranuclear palsy, and frontotemporal dementia (2017) · cites this paper as [22]
The Discussion (page unavailable) reports pallidal atrophy in CBD and apparent cerebellar-region atrophy in PSP, supporting involvement of some named regions. It does not establish that these regions are more affected in CBD and PSP than in FTD. This MRI study also does not report CXCR4 or EGFR transcript levels, although the multiple citations do not identify this paper as the source of that finding. (LLM, conf=0.83)
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- Authors
- Josephs, K. A., Whitwell, J. L., Dickson, D. W., Boeve, B. F., Knopman, D. S., Petersen, R. C., Parisi, J. E., & Jack, C. R.
- Affiliations
- Mayo Clinic (US)
- Mayo Clinic in Florida (US)
- Corresponding author
- Josephs, Keith A.
- ORCID
- Venue
- Neurobiology of Aging
- Publisher
- Elsevier BV
- Published
- 2008-02
- Volume
- 29
- Issue
- 2
- Pages
- 280-289
- ISSN
- 0197-4580 (ISSN-L)
- PMC
- PMC2702857
- OpenAlex
- W2076342549
- Cited by
- 234
- References
- 1
- Citations by year
- 2026: 5 · 2025: 9 · 2024: 9 · 2023: 10 · 2022: 12 · 2021: 10 · 2020: 11 · 2019: 14 · 2018: 5 · 2017: 16 · 2016: 14 · 2015: 11 · 2014: 15 · 2013: 19 · 2012: 9
- FWCI
- 6.73
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Neurobiology of Aging (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Mayo Foundation for Medical Education and Research
- National Institutes of Health
- National Institute on Aging (R01AG11378, P50‐AG16574, U01AG06786, U01AG006786, R01AG011378, P50AG016574)
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (K12HD049078, K12 HD 49078)
- Topics
- Health Sciences › Medicine › Neurology › Parkinson's Disease Mechanisms and Treatments
- Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
- Life Sciences › Neuroscience › Neurology › Neurological diseases and metabolism
- Keywords
- progressive supranuclear palsy, corticobasal degeneration, brain atrophy patterns, gray matter atrophy, white matter atrophy, brainstem atrophy, extrapyramidal symptoms, dementia syndromes, regional brain atrophy
- MeSH terms
- Aged, Aged, 80 and over, Autopsy, Basal Ganglia, Cerebral Cortex, Female, Humans, Magnetic Resonance Imaging, Male, Middle Aged, Supranuclear Palsy, Progressive, Statistics, Nonparametric, Neurodegenerative Diseases, Imaging, Three-Dimensional
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