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In this study, a total 349 participants were recruited from Guangzhou health aging and dementia cohort from March 2020 to March 2024, including participants with or without cognitive impairment. All participants underwent detailed cognitive assessment including MMSE, MoCA, Clinical Dementia Rating (CDR), Functional Activities Questionnaire (FAQ), MemTrax, blood tests, and neuroimaging including MRI, PET/CT (Florbetapir and Fludeoxyglucose ).
Materials and methods Participants were enrolled continuously between September 2019 and April 2021. All participants were recruited through in-person discussion with patients who volunteered to participate in the study on the in-patient ward before their first chemotherapy session in the First Affiliated Hospital of Kunming Medical University.
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