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Updated: Jan 10, 2026

Quantitative 3D In Silico Modeling q3DISM of Cerebral Amyloid-beta Phagocytosis in Rodent Models of Alzheimer's Disease
Published on: December 26, 2016
Inflammatory Alterations and Multidomain Cognition in Alzheimer Disease and Related Dementias
Anna Smith1, Diana Guzman, Seonjoo Lee
1Department of Neurology, Taub Institute for Research on Alzheimer's Disease and the Aging Brain, G.H. Sergievsky Center, Columbia University Irving Medical Center, New York, NY.
Objective:
To determine how 18kDa Translocator (TSPO) PET, which measures inflammatory alterations, is associated with domain-specific cognition in the presence and absence of elevated amyloid.
Methods:
This cross-sectional study uses data collected on 46 adults aged 50 and over who underwent TSPO PET (11C-ER176 SUVR) and amyloid PET (18F-Florbetaben SUVR) as well as medical, neurological, and neuropsychological assessments. Controls (n=21) were amyloid-negative and cognitively unimpaired while individuals with Alzheimer disease or related dementias (ADRD; n=25) were cognitively impaired, regardless of amyloid positivity. Cognition was assessed using the Mini-Mental State Examination (MMSE) and domain-specific tests included in the NACC UDSv3.
Results:
Greater TSPO is associated with lower performance in episodic memory, attention/processing speed, executive function, language, and visuospatial ability in amyloid-positive individuals, but restricted to episodic memory in amyloid-negative individuals.
Conclusion:
Targeting microglia as an additional or alternative strategy for cognitive impairment in Alzheimer disease and related dementias may provide further benefits, even in amyloid-negative individuals.
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