4.7 Article

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

Journal

Publisher

SPRINGER
DOI: 10.1007/s00259-021-05669-6

Keywords

Early-onset; Alzheimer's disease; [F-18]flortaucipir; Tau pathology; Cerebral blood flow; Cognition

Funding

  1. ZonMW Memorabel grant

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Compared to LOAD, EOAD patients exhibit higher tau pathology levels but lower relative cerebral blood flow values, particularly in the medial temporal regions. The associations between lateral temporal and occipitoparietal tau pathology and relative cerebral blood flow with cognitive impairment are stronger in EOAD than in LOAD, suggesting different mechanisms underlying cognitive deficits in the two subtypes of Alzheimer's disease.
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 [F-18]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 [F-18]flortaucipir PET scan and extensive neuropsychological assessment. We extracted binding potentials (BPND) 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 BPND 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 BPND/R-1 on cognition. Results Both region-of-interest and voxel-wise contrasts showed higher [F-18]flortaucipir BPND 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 BPND - 0.76 <= st beta <= - 0.48 vs LOAD - 0.18 <= st beta <= - 0.02; EOAD R-1 0.37 <= st beta <= 0.84 vs LOAD - 0.25 <= st beta <= 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.

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