Free water derived by multi‐shell diffusion MRI reflects tau/neuroinflammatory pathology in Alzheimer's disease

Introduction Free‐water (FW) imaging, a new analysis method for diffusion magnetic resonance imaging (MRI), can indicate neuroinflammation and degeneration. We evaluated FW in Alzheimer's disease (AD) using tau/inflammatory and amyloid positron emission tomography (PET). Methods Seventy‐one par...

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Published inAlzheimer's & dementia : translational research & clinical interventions Vol. 8; no. 1; pp. e12356 - n/a
Main Authors Nakaya, Moto, Sato, Noriko, Matsuda, Hiroshi, Maikusa, Norihide, Shigemoto, Yoko, Sone, Daichi, Yamao, Tensho, Ogawa, Masayo, Kimura, Yukio, Chiba, Emiko, Ohnishi, Masahiro, Kato, Koichi, Okita, Kyoji, Tsukamoto, Tadashi, Yokoi, Yuma, Sakata, Masuhiro, Abe, Osamu
Format Journal Article
LanguageEnglish
Published Hoboken John Wiley & Sons, Inc 2022
John Wiley and Sons Inc
Wiley
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Summary:Introduction Free‐water (FW) imaging, a new analysis method for diffusion magnetic resonance imaging (MRI), can indicate neuroinflammation and degeneration. We evaluated FW in Alzheimer's disease (AD) using tau/inflammatory and amyloid positron emission tomography (PET). Methods Seventy‐one participants underwent multi‐shell diffusion MRI, 18F‐THK5351 PET, 11C‐Pittsburgh compound B PET, and neuropsychological assessments. They were categorized into two groups: healthy controls (HCs) (n = 40) and AD‐spectrum group (AD‐S) (n = 31) using the Centiloid scale with amyloid PET and cognitive function. We analyzed group comparisons in FW and PET, correlations between FW and PET, and correlation analysis with neuropsychological scores. Results In AD‐S group, there was a significant positive correlation between FW and 18F‐THK5351 in the temporal lobes. In addition, there were negative correlations between FW and cognitive function in the temporal lobe and cingulate gyrus, and negative correlations between 18F‐THK5351 and cognitive function in the same regions. Discussion FW imaging could be a biomarker for tau in AD alongside clinical correlations.
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ISSN:2352-8737
2352-8737
DOI:10.1002/trc2.12356