Distribution of brain atrophy in behavioral variant frontotemporal dementia
Abstract
Marked brain atrophy occurs in frontotemporal dementia (FTD) yet substantial variation between cases is seen. Recently, a four-level staging scheme which reflects increasing disease duration, severity of dementia and degree of neurodegeneration was described. In the present study, the extent and magnitude of atrophy in behavioral variant FTD and its relationship to disease duration and pathological subtype was further evaluated by quantifying the volume of 30 anatomically-defined regions. A validated point count technique was applied to 17 patients with FTD (9 Pick's disease, 6 dementia lacking distinctive histology, 2 FTD with motor neuron disease) and 21 controls. Atrophy was seen in all brain regions except the inferior frontal cortex and area 37. As might be expected, increasing severity of atrophy occurred with increasing disease duration and stage however measurable atrophy was more widespread than indicated by the staging scheme. Furthermore, severity of atrophy was not related to pathological subtype. Frontal, limbic and temporal regions appeared to be severely affected early in the disease process with temporal lobe atrophy the best predictor of disease duration. White matter, more posterior regions and the subcortex were affected later in the disease. These findings demonstrate a pattern of selective vulnerability which progresses over time. Furthermore, they demonstrate that although patients with a similar clinical subtype may have differing underlying histopathology, the pattern, severity and progression of brain atrophy is the same. This suggests that the regional pattern of neurodegeneration, rather than the type of histopathology influences the clinical syndrome in FTD.
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Regional grey matter atrophy patterns are known to be heterogeneous in bvFTD, and a cross-sectional study suggested at least four distinct data-driven subtypes.
“However, since many years regional GM atrophy patterns are known to be heterogeneous in bvFTD, of which a cross-sectional study suggested at least four distinct (data-driven) subtypes (Kril et al., 2005; Ranasinghe et al., 2021).”
From The pursuit for markers of disease progression in behavioral variant frontotemporal dementia: a scoping review to optimize outcome measures for clinical trials (2024) · cites this paper as Kril et al., 2005
In bvFTD, a cross-sectional study suggested at least four distinct data-driven subtypes.
“in bvFTD, of which a cross-sectional study suggested at least four distinct (data-driven) subtypes (Kril et al., 2005; Ranasinghe et al., 2021).”
From The pursuit for markers of disease progression in behavioral variant frontotemporal dementia: a scoping review to optimize outcome measures for clinical trials (2024) · cites this paper as Kril et al., 2005
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References 41 · Cited by 83
- Authors
- Kril, J. J., Macdonald, V., Patel, S., Png, F., & Halliday, G. M.
- Affiliations
- The University of Sydney (AU)
- UNSW Sydney (AU)
- Corresponding author
- Kril, Jillian J.
- Venue
- Journal of the Neurological Sciences
- Publisher
- Elsevier BV
- Published
- 2005-05
- Volume
- 232
- Issue
- 1-2
- Pages
- 83-90
- ISSN
- 0022-510X (ISSN-L)
- OpenAlex
- W2075075098
- Cited by
- 83
- References
- 41
- Citations by year
- 2026: 1 · 2025: 1 · 2024: 3 · 2022: 1 · 2021: 3 · 2020: 4 · 2019: 5 · 2018: 2 · 2017: 2 · 2016: 7 · 2015: 2 · 2014: 7 · 2013: 7 · 2012: 5
- FWCI
- 3.60
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of the Neurological Sciences (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Health and Medical Research Council
- Topics
- Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
- Health Sciences › Medicine › Neurology › Amyotrophic Lateral Sclerosis Research
- Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
- Keywords
- behavioral variant frontotemporal dementia, brain atrophy, disease duration, Pick's disease, temporal lobe atrophy, white matter atrophy, subcortical atrophy, histological subtypes, neurodegeneration
- MeSH terms
- Aged, Atrophy, Brain, Dementia, Female, Frontal Lobe, Humans, Male, Middle Aged, Nerve Degeneration, Phenotype, Temporal Lobe, Motor Neuron Disease, Disease Progression, Pick Disease of the Brain
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