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  • Online Resource  (2)
  • Visser, Denise  (2)
  • Windhorst, Albert D.  (2)
  • van Der Flier, Wiesje  (2)
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  • Online Resource  (2)
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  • 1
    In: Alzheimer's & Dementia, Wiley, Vol. 16, No. S6 ( 2020-12)
    Abstract: Early‐onset Alzheimer’s disease (AD) dementia is characterized by a heterogeneous cognitive profile consisting of language and visuo‐spatial impairment. Spatial patterns of tau pathology measured with [18F]flortaucipir may help to explain the heterogeneity within early‐onset AD. Method Seventy‐one patients with Alzheimer’s disease dementia patients (n=28 early‐onset age=58, MMSE=22; n=43 late‐onset age=71, MMSE=23), of whom 6 patients with posterior cortical atrophy, 2 behavioral of AD (bvAD). All patients had available 130 minutes [18F]flortaucipir PET scans and extensive neuropsychological assessment. We generated parametric images and non‐displaceable binding potentials (BPnd) were extracted using receptor parametric mapping in the following brain regions; frontal, occipital, parietal, medial and lateral temporal cortex. We performed principal component analyses to reduce 12 cognitive tests into latent variables which reflect (uncorrelated) cognitive functions. ANOVA and linear regressions were performed to investigate between [18F] flortaucipir group differences and associations with cognition functions. Result Early‐onset AD dementia patients showed increased [18F] flortaucipir BPnd in occipital, parietal and frontal cortex (all p 〈 0.001) compared to late‐onset AD. Across all AD patients, adjusted for education, sex and age, frontal [18F]flortaucipir BPnd was associated with attention (p=0.003), occipital [18F] flortaucipir BPnd with visual scanning and memory (both p=0.01), parietal [18F]flortaucipir BPnd with attention and visual scanning (p=0.002 and p=0.02 respectively). Lateral temporal [18F] flortaucipir BPnd was associated with attention (p=0.006) and medial temporal [18F]flortaucipir BPnd with memory (p=0.01). Interaction effects were found for occipital and parietal [18F] flortaucipir BPnd and visual scanning for early‐onset AD, and parietal [18F]flortaucipir BPnd and attention for late‐onset. Frontal [18F] flortaucipir BPnd was associated with visual scanning in late‐onset AD. In an exploratory analysis, we found higher [18F]flortaucipir BPnd in parieto‐occipital cortices in PCA compared early‐ and late‐onset AD (both p 〈 0.001). Conclusion Differential spatial patterns of tau pathology were found depending on age‐of‐onset. Tau pathology may help to explain the clinical phenotype of early and late‐onset AD.
    Type of Medium: Online Resource
    ISSN: 1552-5260 , 1552-5279
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2020
    detail.hit.zdb_id: 2201940-6
    Location Call Number Limitation Availability
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  • 2
    In: Alzheimer's & Dementia, Wiley, Vol. 16, No. S1 ( 2020-12)
    Abstract: Dementia with Lewy Bodies (DLB) is characterized by the presence of neuronal inclusions containing alpha‐synuclein proteins, and often co‐occurs with Alzheimer’s disease (AD) pathology. We aimed to determine the pattern of tau pathology and relative cerebral blood flow (rCBF) in DLB, compared to AD and controls, and their association with cognitive impairment using a single dynamic [ 18 F]flortaucipir PET scan. Method Eighteen patients with DLB (66 ± 8 years, MMSE 25 ± 4, 44% amyloid positive (abnormal CSF (Aβ42 〈 813 pg/mL)/visual read amyloid‐PET), 100% FP‐CIT SPECT abnormal, Table 1), 65 amyloid positive cognitively impaired patients (MCI‐AD (n = 13), AD (n = 52)) and 50 controls underwent a dynamic 130‐minute [ 18 F]flortaucipir PET scan. Receptor parametric mapping (cerebellar gray matter reference region) was used to extract (regional, Hammers based) binding potential (BP ND ) and R 1 , which reflect tau pathology and rCBF, respectively. We performed voxel‐wise comparisons (P uncorrected   〈  0.001) of [ 18 F]flortaucipir BP ND and R 1 between diagnostic groups using SPM, adjusted for age and sex. DLB patients underwent extensive neuropsychological assessment covering memory, executive functioning, language, attention and visuospatial domains. For DLB only, we performed linear regression analyses between [ 18 F]flortaucipir BP ND , R 1 and cognition in the following regions‐of‐interest (ROIs); medial and lateral temporal/ parietal, occipital and frontal cortex, adjusted for age, sex and education. Result Averaged [ 18 F]flortaucipir BP ND images across groups showed visually minimal tau uptake in the inferior temporal lobe in DLB (Figure 1). Voxel‐wise comparisons showed lower [ 18 F]flortaucipir R 1 in the occipital lobe in DLB compared to AD and controls (Figure 2). Regional [ 18 F]flortaucipir BP ND was lower in DLB compared to AD and comparable with tau binding in controls (Figure 3). Occipital and lateral parietal R 1 was lower in DLB compared to AD and controls (all p 〈 0.01, Figure 3). R 1 but not BP ND was related to cognition (language only); lower medial temporal (stß = 0.76, p = 0.001), medial parietal (stß = 0.64, p = 0.02) and frontal (stß = 0.64, p = 0.02) R 1 was related to lower language score (Figure 4). Conclusion In our sample, tau load in patients with DLB did not differ from controls, but there were DLB‐specific occipital and lateral parietal flow reductions compared to both controls and AD patients. Our results indicate that rCBF may be of more clinical relevance than tau pathology in DLB.
    Type of Medium: Online Resource
    ISSN: 1552-5260 , 1552-5279
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2020
    detail.hit.zdb_id: 2201940-6
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
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