Journal Article DZNE-2020-07392

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Functional network resilience to pathology in presymptomatic genetic frontotemporal dementia.

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2019
Elsevier Science Amsterdam [u.a.]

Neurobiology of aging 77, 169-177 () [10.1016/j.neurobiolaging.2018.12.009]

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Abstract: The presymptomatic phase of neurodegenerative diseases are characterized by structural brain changes without significant clinical features. We set out to investigate the contribution of functional network resilience to preserved cognition in presymptomatic genetic frontotemporal dementia. We studied 172 people from families carrying genetic abnormalities in C9orf72, MAPT, or PGRN. Networks were extracted from functional MRI data and assessed using graph theoretical analysis. We found that despite loss of both brain volume and functional connections, there is maintenance of an efficient topological organization of the brain's functional network in the years leading up to the estimated age of frontotemporal dementia symptom onset. After this point, functional network efficiency declines markedly. Reduction in connectedness was most marked in highly connected hub regions. Measures of topological efficiency of the brain's functional network and organization predicted cognitive dysfunction in domains related to symptomatic frontotemporal dementia and connectivity correlated with brain volume loss in frontotemporal dementia. We propose that maintaining the efficient organization of the brain's functional network supports cognitive health even as atrophy and connectivity decline presymptomatically.

Keyword(s): Adult (MeSH) ; Aged (MeSH) ; Atrophy (MeSH) ; Brain: diagnostic imaging (MeSH) ; Brain: pathology (MeSH) ; Brain: physiopathology (MeSH) ; C9orf72 Protein: genetics (MeSH) ; Cognition (MeSH) ; Female (MeSH) ; Frontotemporal Dementia: genetics (MeSH) ; Frontotemporal Dementia: pathology (MeSH) ; Frontotemporal Dementia: psychology (MeSH) ; Heterozygote (MeSH) ; Humans (MeSH) ; Magnetic Resonance Imaging (MeSH) ; Male (MeSH) ; Middle Aged (MeSH) ; Nerve Net: diagnostic imaging (MeSH) ; Nerve Net: pathology (MeSH) ; Nerve Net: physiopathology (MeSH) ; Neuroimaging (MeSH) ; Organ Size (MeSH) ; tau Proteins: genetics (MeSH) ; C9orf72 Protein ; C9orf72 protein, human ; MAPT protein, human ; tau Proteins

Classification:

Contributing Institute(s):
  1. Core ICRU (Core ICRU)
Research Program(s):
  1. 342 - Disease Mechanisms and Model Systems (POF3-342) (POF3-342)

Appears in the scientific report 2019
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Medline ; Creative Commons Attribution CC BY 4.0 ; OpenAccess ; BIOSIS Previews ; Clarivate Analytics Master Journal List ; Current Contents - Life Sciences ; Ebsco Academic Search ; IF >= 5 ; JCR ; NationallizenzNationallizenz ; SCOPUS ; Web of Science Core Collection
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 Record created 2020-02-18, last modified 2024-03-21


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