Disruption of macroscale functional network organisation in patients with frontotemporal dementia

Neurodegenerative dementias have a profound impact on higher-order cognitive and behavioural functions. Investigating macroscale functional networks through cortical gradients provides valuable insights into the neurodegenerative dementia process and overall brain function. This approach allows for the exploration of unimodal-multimodal differentiation and the intricate interplay between functional brain networks. We applied cortical gradients mapping to resting-state functional MRI data of patients with frontotemporal dementia (FTD) (behavioural-bvFTD, non-fluent and semantic) and healthy controls. In healthy controls, the principal gradient maximally distinguished sensorimotor from default-mode network (DMN) and the secondary gradient visual from salience network (SN). In all FTD variants, the principal gradient's unimodal-multimodal differentiation was disrupted. The secondary gradient, however, showed widespread disruptions impacting the interactions among all networks specifically in bvFTD, while semantic and non-fluent variants exhibited more focal alterations in limbic and sensorimotor networks. Additionally, the visual network showed responsive and/or compensatory changes in all patients. Importantly, these disruptions extended beyond atrophy distribution and related to symptomatology in patients with bvFTD. In conclusion, optimal brain function requires networks to operate in a segregated yet collaborative manner. In FTD, our findings indicate a collapse and loss of differentiation between networks not solely explained by atrophy. These specific cortical gradients' fingerprints could serve as a functional signature for identifying early changes in neurodegenerative diseases or potential compensatory processes.

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Publication Details

Journal
Molecular Psychiatry
Published
2024-11-23
DOI
https://doi.org/10.1038/s41380-024-02847-4
Citations
8
Primary Topic
Functional Brain Connectivity Studies
Type
article
Field-Weighted Citation Impact
2.74

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article

Disruption of macroscale functional network organisation in patients with frontotemporal dementia

Vincent Le Du, Raffaella Migliaccio, Daniel S. Margulies, Bénédicte Batrancourt et al.
8 citations
Molecular Psychiatry
Functional Brain Connectivity Studies
2.74
article

Disruption of macroscale functional network organisation in patients with frontotemporal dementia

Vincent Le Du, Raffaella Migliaccio, Daniel S. Margulies, Bénédicte Batrancourt, Valérie Godefroy, Marion Houot, Arabella Bouzigues, Jason D. Warren, Lucy Louise Russell, Jonathan D. Rohrer, Isabelle Le Ber, Richard Lévy
article en
8 citations

Abstract

Neurodegenerative dementias have a profound impact on higher-order cognitive and behavioural functions. Investigating macroscale functional networks through cortical gradients provides valuable insights into the neurodegenerative dementia process and overall brain function. This approach allows for the exploration of unimodal-multimodal differentiation and the intricate interplay between functional brain networks. We applied cortical gradients mapping to resting-state functional MRI data of patients with frontotemporal dementia (FTD) (behavioural-bvFTD, non-fluent and semantic) and healthy controls. In healthy controls, the principal gradient maximally distinguished sensorimotor from default-mode network (DMN) and the secondary gradient visual from salience network (SN). In all FTD variants, the principal gradient's unimodal-multimodal differentiation was disrupted. The secondary gradient, however, showed widespread disruptions impacting the interactions among all networks specifically in bvFTD, while semantic and non-fluent variants exhibited more focal alterations in limbic and sensorimotor networks. Additionally, the visual network showed responsive and/or compensatory changes in all patients. Importantly, these disruptions extended beyond atrophy distribution and related to symptomatology in patients with bvFTD. In conclusion, optimal brain function requires networks to operate in a segregated yet collaborative manner. In FTD, our findings indicate a collapse and loss of differentiation between networks not solely explained by atrophy. These specific cortical gradients' fingerprints could serve as a functional signature for identifying early changes in neurodegenerative diseases or potential compensatory processes.

Molecular PsychiatryVol. 30(6)
Université Claude Bernard Lyon 1 (FR), Centre National de la Recherche Scientifique (FR), Inserm (FR), Université Paris Cité (FR), Sorbonne Université (FR), University of Oxford (GB), Centre de Recherche en Neurosciences de Lyon (FR), Assistance Publique – Hôpitaux de Paris (FR), Wellcome Centre for Integrative Neuroimaging (GB), UK Dementia Research Institute (GB), National Hospital for Neurology and Neurosurgery (GB), Institut du Cerveau (FR), Fondation pour l’innovation en Cadiométabolisme et Nutrition (FR), University College London (GB)
Wellcome Trust, EU Joint Programme – Neurodegenerative Disease Research, Brain Research UK, Fondation Vaincre Alzheimer, Alzheimer's Society, National Institute for Health and Care Research, European Commission, Agence Nationale de la Recherche, Fondation pour la Recherche Médicale, University College London Hospitals NHS Foundation Trust, Fondation pour la Recherche sur Alzheimer, Medical Research Council
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Openalex Percentile: Top 9%
Functional Brain Connectivity Studies
2.74
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