Relationships Between the Deposition of Amyloid-β and Tau Protein and Glymphatic System Activity in Alzheimer's Disease: Diffusion Tensor Image Study.

Background: Amyloid-β (Aβ) and tau protein accumulation in the brain is thought to be one of the causes of Alzheimer's disease (AD). Recent study found that the glymphatic system was waste drainage system in the brain and promoting the elimination of Aβ and tau protein.Objective: We evaluated the re...

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Publicado en:Journal of Alzheimer's Disease Vol. 90; no. 1; pp. 295 - 304
Autores principales: Ota, Miho, Sato, Noriko, Nakaya, Moto, Shigemoto, Yoko, Kimura, Yukio, Chiba, Emiko, Yokoi, Yuma, Tsukamoto, Tadashi, Matsuda, Hiroshi
Formato: research tables/charts Journal Article
Publicado: Sage Publications Inc. 2022
Acceso en línea:Ver este registro en EBSCOhost
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      jtl: Journal of Alzheimer's Disease
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      dt: 2022
      vid: 90
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      pub: Sage Publications Inc.
      place: Thousand Oaks, California
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        10.3233/JAD-220534
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        159931711
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      tig:
        atl: Relationships Between the Deposition of Amyloid-β and Tau Protein and Glymphatic System Activity in Alzheimer's Disease: Diffusion Tensor Image Study.
      aug:
        au:
          Ota, Miho
          Sato, Noriko
          Nakaya, Moto
          Shigemoto, Yoko
          Kimura, Yukio
          Chiba, Emiko
          Yokoi, Yuma
          Tsukamoto, Tadashi
          Matsuda, Hiroshi
        affil: Department of Radiology, National Center of Neurology and Psychiatry, Kodaira, Tokyo, Japan
      sug:
        subj:
          Alzheimer's Disease
          Alzheimer's Disease Metabolism
          Peptides Metabolism
          Tomography, Emission-Computed Methods
          Nerve Tissue Proteins Metabolism
          Magnetic Resonance Imaging Methods
          Human
      ab: Background: Amyloid-β (Aβ) and tau protein accumulation in the brain is thought to be one of the causes of Alzheimer's disease (AD). Recent study found that the glymphatic system was waste drainage system in the brain and promoting the elimination of Aβ and tau protein.Objective: We evaluated the relationships between the glymphatic system activity and the Aβ and tau protein deposition.Methods: Subjects were 21 patients with AD and 36 healthy subjects who underwent diffusion tensor imaging (DTI) scan and the positron emission tomography (PET) using with the Aβ tracer: 11C-PiB and the tau/inflammatory tracer: 18F-THK5351. We computed diffusion tensor image analysis along the perivascular space (DTI-ALPS) index as the proxy of glymphatic system activity, and estimated the relationships between the DTI-ALPS index and Aβ and tau protein/inflammatory deposition.Results: We found significant negative correlations between DTI-ALPS index and the standard uptake value ratio (SUVR) of 11C-PiB in the bilateral temporal and left parietal cortices and left posterior cingulate gyrus in all subjects. Further, we detected significant negative correlations between DTI-ALPS index and the SUVR of 18F-THK5351 in the bilateral temporal cortices and right parietal cortex in all participants, too.Conclusion: Our data suggested that DTI-ALPS index was a good biomarker for the evaluation of Aβ and tau deposition and neuroinflammation, and this marker might be effective to estimate the glymphatic system activity.
      pubtype: Academic Journal
      doctype:
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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