Please use this identifier to cite or link to this item: http://bura.brunel.ac.uk/handle/2438/32374
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dc.contributor.authorKonwar, S-
dc.contributor.authorHunyadvari, N-
dc.contributor.authorVenneri, A-
dc.contributor.authorCole, JH-
dc.contributor.authorBocchetta, M-
dc.contributor.authorFrontotemporal Lobar Degeneration Neuroimaging Initiative-
dc.contributor.author4-Repeat Tauopathy Neuroimaging Initiative-
dc.date.accessioned2025-11-19T10:06:52Z-
dc.date.available2025-11-19T10:06:52Z-
dc.date.issued2025-09-23-
dc.identifierORCiD: Annalena Venneri https://orcid.org/0000-0002-9488-2301-
dc.identifierORCiD: Martina Bocchetta-
dc.identifierArticle number: 642-
dc.identifier.citationKonwar, 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.en_US
dc.identifier.issn0340-5354-
dc.identifier.urihttps://bura.brunel.ac.uk/handle/2438/32374-
dc.descriptionData 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.en_US
dc.descriptionSupplementary Information is available online at: https://link.springer.com/article/10.1007/s00415-025-13378-5#Sec26 (DOCX 36194 KB).-
dc.description.abstractIntroduction: 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.en_US
dc.description.sponsorshipThis work was primarily funded by the BRUNEL RESEARCH INITIATIVE & ENTERPRISE FUND (BRIEF) 2023/24 (12796115). M.B. was also supported by a Fellowship award from the Alzheimer’s Society, UK (AS-JF-19a-004-517) and a grant from Alzheimer’s Research UK (ARUK-PPG2023B-013). A.V. acknowledges the support by funding obtained under the National Recovery and Resilience Plan (NRRP), Mission 4 Component 2 Investment 1.3—Call for tender No. 341 of 15/03/2022 of the Italian Ministry of University and Research funded by the European Union-NextGenerationEU, Project code PE0000006, Concession Decree No. 1553 of 11/10/2022 adopted by the Italian Ministry of University and Research, CUP D93C22000930002, “A multiscale integrated approach to the study of the nervous system in health and disease” (MNESYS). Data collection and sharing for this project were funded by the Frontotemporal Lobar Degeneration Neuroimaging Initiative (National Institutes of Health Grant R01 AG032306) and by the 4-Repeat Tauopathy Neuroimaging Initiative (4RTNI) (National Institutes of Health Grant R01 AG038791) and through generous contributions from the Tau Research Consortium. FTLDNI and 4RTNI studies are coordinated through the University of California, San Francisco, Memory and Aging Center. FTLDNI and 4RTNI data are disseminated by the Laboratory for Neuro Imaging at the University of Southern California.en_US
dc.format.extent1 - 17-
dc.format.mediumPrint-Electronic-
dc.languageEnglish-
dc.language.isoen_USen_US
dc.publisherSpringer Natureen_US
dc.rightsCreative Commons Attribution 4.0 International-
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/-
dc.subjectfrontotemporal lobar degenerationen_US
dc.subjectneuroanatomical normative modellingen_US
dc.subjectindividual neuroimaging biomarkersen_US
dc.subjectMRIen_US
dc.titleNeuroanatomical normative modelling in frontotemporal lobar degeneration: higher heterogeneity in the behavioural varianten_US
dc.typeArticleen_US
dc.date.dateAccepted2025-09-05-
dc.identifier.doihttps://doi.org/10.1007/s00415-025-13378-5-
dc.relation.isPartOfJournal of Neurology-
pubs.issue10-
pubs.publication-statusPublished-
pubs.volume272-
dc.identifier.eissn1432-1459-
dc.rights.licensehttps://creativecommons.org/licenses/by/4.0/legalcode.en-
dcterms.dateAccepted2025-09-05-
dc.rights.holderThe Author(s)-
Appears in Collections:Dept of Life Sciences Research Papers

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