Network interdigitations of Tau and amyloid-beta deposits define cognitive levels in aging

Amyloid-beta (Aβ) plaques and tau neurofibrillary tangles are pathological hallmarks of Alzheimer's disease (AD); their contribution to neurodegeneration and clinical manifestations are critical in understanding preclinical AD. At present, the mechanisms related to Aβ and tau pathogenesis leadi...

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Detalles Bibliográficos
Autores: Kim, Chan-Mi|||0000-0001-5686-1668, Montal, Victor|||0000-0002-5714-9282, Diez, Ibai, Orwig, William, Sepulcre, Jorge|||0000-0002-4199-2304
Tipo de recurso: artículo
Fecha de publicación:2021
País:España
Institución:Universitat Autònoma de Barcelona
Repositorio:Dipòsit Digital de Documents de la UAB
Idioma:inglés
OAI Identifier:oai:ddd.uab.cat:243795
Acceso en línea:https://ddd.uab.cat/record/243795
https://dx.doi.org/urn:doi:10.1002/hbm.25350
Access Level:acceso abierto
Palabra clave:Aging
Alzheimer's disease
Amyloid PET
Cognition
Connectivity analysis
Tau PET
Descripción
Sumario:Amyloid-beta (Aβ) plaques and tau neurofibrillary tangles are pathological hallmarks of Alzheimer's disease (AD); their contribution to neurodegeneration and clinical manifestations are critical in understanding preclinical AD. At present, the mechanisms related to Aβ and tau pathogenesis leading to cognitive decline in older adults remain largely unknown. Here, we examined graph theory-based positron emission tomography (PET) analytical approaches, within and between tau and Aβ PET modalities, and tested the effects on cognitive changes in cognitively normal older adults (CN). Particularly, we focused on the network interdigitations of Aβ and tau deposits, along with cognitive test scores in CN at both baseline and 2-year follow-up (FU). We found highly significant Aβ-tau network integrations in AD vulnerable areas, as well as significant associations between those Aβ-tau interdigitations and general cognitive impairment in CN at baseline and FU. Our findings suggest a distinctive contribution of interlinking network relationships between Aβ and tau deposits in heteromodal areas of the human brain. They support a network-based interaction between Aβ and tau accumulations as a key factor for cognitive deterioration in CN prior to dementia. We examined network interaction patterns within single positron emission tomography (PET) modality, such as Aß-to-Aß or Tau-to-Tau correlations, and between different PET modalities, such as Aß-to-Tau or Tau-to-Aß, at high-resolution (voxel-level) in cognitively normal older adults (CN), using a graph theory-based analysis. We observed that the PET uptakes derived from Aß-to-Tau interdigitations were significantly associated with Alzheimer's Disease Assessment Scale-Cognitive Subscale in AD vulnerable brain areas, a finding confirmed by our longitudinal investigation. Therefore, our work suggests the preceding contribution of network interactions between Aß and tau deposits to explain initial cognitive changes in CN prior to the conversion of dementia.