Please use this identifier to cite or link to this item: http://bura.brunel.ac.uk/handle/2438/32374
Title: Neuroanatomical normative modelling in frontotemporal lobar degeneration: higher heterogeneity in the behavioural variant
Authors: Konwar, S
Hunyadvari, N
Venneri, A
Cole, JH
Bocchetta, M
Frontotemporal Lobar Degeneration Neuroimaging Initiative
4-Repeat Tauopathy Neuroimaging Initiative
Keywords: frontotemporal lobar degeneration;neuroanatomical normative modelling;individual neuroimaging biomarkers;MRI
Issue Date: 23-Sep-2025
Publisher: Springer Nature
Citation: Konwar, S. et al for the Frontotemporal Lobar Degeneration Neuroimaging Initiative and for the 4-Repeat Tauopathy Neuroimaging Initiative (2025) 'Neuroanatomical normative modelling in frontotemporal lobar degeneration: higher heterogeneity in the behavioural variant', Journal of Neurology, 272 (10), 642, pp. 1 - 17. doi: 10.1007/s00415-025-13378-5.
Abstract: Introduction: Frontotemporal lobar degeneration (FTLD) includes heterogenous diseases: behavioural variant frontotemporal dementia (bvFTD), primary progressive aphasias (PPA), progressive supranuclear palsy (PSP) and corticobasal syndrome (CBS). We applied neuroanatomical normative modelling to quantify individual atrophy patterns and heterogeneity within and between FTLD forms. Methods: We included 160 participants across FTLDNI and 4RTNI studies: controls (n = 15), bvFTD (n = 22), nfvPPA (n = 14), svPPA (n = 21), CBS (n = 43) and PSP (n = 45). Using cortical thickness and subcortical volumes from 3T MRIs, we applied normative modelling with a large healthy reference dataset (n = 58,836), further accounting for age, sex, and scanner. Outlier regions (z < – 1.96) were used to compute total outlier counts (tOC) and Hamming distances, capturing individual atrophy patterns and inter-subject dissimilarity. Results: bvFTD, svPPA, CBS and PSP showed significantly higher cortical tOC than controls, with all groups showing higher subcortical tOC than controls, especially svPPA and PSP. bvFTD, svPPA, CBS and PSP had significantly higher cortical Hamming distance scores than controls, with higher scores in bvFTD and svPPA than nfvPPA and PSP. svPPA and PSP had significantly higher subcortical scores than controls and CBS. Greater disease severity (measured using the Clinical Dementia Rating—CDR for PSP and CBS, and the CDR® plus NACC-FTLD global scores for FTD variants) was associated with increased tOC and dissimilarity, highlighting the link between clinical progression and neuroanatomical heterogeneity. Conclusions: The pronounced heterogeneity within and between FTLD subtypes (particularly in bvFTD) increases with disease progression and may reflect distinct underlying pathologies. This supports the development of subtype-specific biomarkers and emphasize the need for personalized diagnostic and therapeutic strategies.
Description: Data availability: Data used in preparation of this article were obtained from the Frontotemporal Lobar Degeneration Neuroimaging Initiative (FTLDNI) and the 4-Repeat Tauopathy Neuroimaging Initiative (4RTNI) databases (https://4rtni-ftldni.ini.usc.edu/ and https://ida.loni.usc.edu/login.jsp). The investigators at FTLDNI and 4RTNI contributed to the design and implementation of FTLDNI and 4RTNI and/or provided data, but did not participate in analysis or writing of this report.
Supplementary Information is available online at: https://link.springer.com/article/10.1007/s00415-025-13378-5#Sec26 (DOCX 36194 KB).
URI: https://bura.brunel.ac.uk/handle/2438/32374
DOI: https://doi.org/10.1007/s00415-025-13378-5
ISSN: 0340-5354
Other Identifiers: ORCiD: Annalena Venneri https://orcid.org/0000-0002-9488-2301
ORCiD: Martina Bocchetta
Article number: 642
Appears in Collections:Dept of Life Sciences Research Papers

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