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Differential associations between neocortical tau pathology and blood flow with cognitive deficits in early-onset vs late-onset Alzheimer’s disease

Denise Visser, Sander C.J. Verfaillie, Emma E. Wolters, Emma M. Coomans, Tessa Timmers, Hayel Tuncel, Ronald Boellaard, Sandeep S.V. Golla, Albert D. Windhorst, Philip Scheltens, Wiesje M. van der Flier, Bart N.M. van Berckel, Rik Ossenkoppele

2022European Journal of Nuclear Medicine and Molecular Imaging23 citationsDOIOpen Access PDF

Abstract

Abstract Purpose Early-onset Alzheimer’s disease (EOAD) and late-onset Alzheimer’s disease (LOAD) differ in neuropathological burden and type of cognitive deficits. Assessing tau pathology and relative cerebral blood flow (rCBF) measured with [ 18 F]flortaucipir PET in relation to cognition may help explain these differences between EOAD and LOAD. Methods Seventy-nine amyloid-positive individuals with a clinical diagnosis of AD (EOAD: n = 35, age-at-PET = 59 ± 5, MMSE = 23 ± 4; LOAD: n = 44, age-at-PET = 71 ± 5, MMSE = 23 ± 4) underwent a 130-min dynamic [ 18 F]flortaucipir PET scan and extensive neuropsychological assessment. We extracted binding potentials (BP ND ) and R 1 (proxy of rCBF) from parametric images using receptor parametric mapping, in medial and lateral temporal, parietal, occipital, and frontal regions-of-interest and used nine neuropsychological tests covering memory, attention, language, and executive functioning. We first examined differences between EOAD and LOAD in BP ND or R 1 using ANOVA (region-of-interest analysis) and voxel-wise contrasts. Next, we performed linear regression models to test for potential interaction effects between age-at-onset and BP ND /R 1 on cognition. Results Both region-of-interest and voxel-wise contrasts showed higher [ 18 F]flortaucipir BP ND values across all neocortical regions in EOAD. By contrast, LOAD patients had lower R 1 values (indicative of more reduced rCBF) in medial temporal regions. For both tau and flow in lateral temporal, and occipitoparietal regions, associations with cognitive impairment were stronger in EOAD than in LOAD (EOAD BP ND − 0.76 ≤ stβ ≤ − 0.48 vs LOAD − 0.18 ≤ stβ ≤ − 0.02; EOAD R 1 0.37 ≤ stβ ≤ 0.84 vs LOAD − 0.25 ≤ stβ ≤ 0.16). Conclusions Compared to LOAD, the degree of lateral temporal and occipitoparietal tau pathology and relative cerebral blood-flow is more strongly associated with cognition in EOAD.

Topics & Concepts

Statistical parametric mappingVoxelAlzheimer's diseaseCardiologyEarly-onset Alzheimer's diseasePsychologyCerebral blood flowCognitive declineNeuroscienceMedicineInternal medicineDementiaNuclear medicineRadiologyMagnetic resonance imagingDiseaseDementia and Cognitive Impairment ResearchFunctional Brain Connectivity StudiesAlzheimer's disease research and treatments