Amyloid-β positron emission tomography can reflect the Amyloid-β protein deposition in the brain and thus serves as one of the golden standards for Alzheimer's disease (AD) diagnosis. However, its practical cost and high radioactivity hinder its application in large-scale early AD screening. Recent neuroscience studies suggest a strong association between changes in functional connectivity network (FCN) derived from functional MRI (fMRI), and deposition patterns of Amyloid-β protein in the brain.
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January 2025
Dementia has high incidence among the elderly, and Alzheimer's disease (AD) is the most common dementia. The procedure of AD diagnosis in clinics usually follows a standard routine consisting of different phases, from acquiring non-imaging tabular data in the screening phase to MR imaging and ultimately to PET imaging. Most of the existing AD diagnosis studies are dedicated to a specific phase using either single or multi-modal data.
View Article and Find Full Text PDFCell replacement is a promising approach for neurodegenerative disease treatment. Somatic cells such as fibroblasts can be induced to differentiate into neurons by specific transcription factors; however, the potential of viral vectors used for reprogramming to integrate into the genome raises concerns about the potential clinical applications of this approach. Here, we directly reprogrammed rat embryonic skin fibroblasts into induced neurons (iNs) via six small-molecule compounds (SMs) (VPA, CHIR99021, forskolin, Y-27632, Repsox, and P7C3-A20).
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