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AbstractBackgroundBasal forebrain (BF) degeneration occurs in Down syndrome (DS)‐associated Alzheimer's disease (AD). However, the dynamics of BF atrophy with age and disease progression, its impact on cognition, and its relationship with AD biomarkers have not been studied in DS.MethodsWe included 234 adults with DS (150 asymptomatic, 38 prodromal AD, and 46 AD dementia) and 147 euploid controls. BF volumes were extracted from T‐weighted magnetic resonance images using a stereotactic atlas in SPM12. We assessed BF volume changes with age and along the clinical AD continuum and their relationship to cognitive performance, cerebrospinal fluid (CSF) and plasma amyloid/tau/neurodegeneration biomarkers, and hippocampal volume.ResultsIn DS, BF volumes decreased with age and along the clinical AD continuum and significantly correlated with amyloid, tau, and neurofilament light chain changes in CSF and plasma, hippocampal volume, and cognitive performance.DiscussionBF atrophy is a potentially valuable neuroimaging biomarker of AD‐related cholinergic neurodegeneration in DS.
volumetry, Adult, neuroimaging, Basal Forebrain, Down syndrome, biomarkers, Neuroimaging, Alzheimer's disease, Alzheimer&apos, s disease, Basal forebrain, Magnetic resonance imaging, Volumetry, cholinergic, Alzheimer Disease, magnetic resonance imaging, Humans, Down Syndrome, Atrophy, basal forebrain, Cholinergic, Biomarkers
volumetry, Adult, neuroimaging, Basal Forebrain, Down syndrome, biomarkers, Neuroimaging, Alzheimer's disease, Alzheimer&apos, s disease, Basal forebrain, Magnetic resonance imaging, Volumetry, cholinergic, Alzheimer Disease, magnetic resonance imaging, Humans, Down Syndrome, Atrophy, basal forebrain, Cholinergic, Biomarkers
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