Differential associations between neocortical tau pathology and blood flow with cognitive deficits in early-onset vs late-onset Alzheimer's disease
Creators
- 1. Department of Radiology & Nuclear Medicine, Amsterdam Neuroscience, Vrije Universiteit Amsterdam, Amsterdam UMC, Amsterdam (Netherlands)
- 2. Department of Neurology, Alzheimer Center Amsterdam, Amsterdam Neuroscience, Vrije Universiteit Amsterdam, Amsterdam UMC, Amsterdam (Netherlands)
- 3. Department of Epidemiology and Biostatistics, Vrije Universiteit Amsterdam, Amsterdam UMC, Amsterdam (Netherlands)
- 4. Clinical Memory Research Unit, Lund University, Lund (Sweden)
Description
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]flortaucipir PET in relation to cognition may help explain these differences between EOAD and LOAD. 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]flortaucipir PET scan and extensive neuropsychological assessment. We extracted binding potentials (BP) and R (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 or R 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/R on cognition. Both region-of-interest and voxel-wise contrasts showed higher [F]flortaucipir BP values across all neocortical regions in EOAD. By contrast, LOAD patients had lower R 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 - 0.76 ≤ stβ ≤ - 0.48 vs LOAD - 0.18 ≤ stβ ≤ - 0.02; EOAD R 0.37 ≤ stβ ≤ 0.84 vs LOAD - 0.25 ≤ stβ ≤ 0.16). 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.
Availability note (English)
Available from: http://dx.doi.org/10.1007/s00259-021-05669-6Additional details
Identifiers
Publishing Information
- Journal Title
- European Journal of Nuclear Medicine and Molecular Imaging
- Journal Volume
- 49
- Journal Issue
- 6
- Journal Page Range
- p. 1951-1963
- ISSN
- 1619-7070
- CODEN
- EJNMA6
INIS
- Country of Publication
- Germany
- Country of Input or Organization
- Germany
- INIS RN
- 53059959
- Subject category
- S62: RADIOLOGY AND NUCLEAR MEDICINE;
- Descriptors DEI
- ATROPHY; BEHAVIOR; BIOLOGICAL MARKERS; BLOOD FLOW; BRAIN; CEREBRAL ARTERIES; DIAGNOSIS; FLUORINE 18; IMAGE PROCESSING; MAPPING; MENTAL DISORDERS; NERVOUS SYSTEM DISEASES; NMR IMAGING; PATHOLOGY; POSITRON COMPUTED TOMOGRAPHY; RADIOPHARMACEUTICALS; RECEPTORS; RELAXATION TIME; WEIGHTING FUNCTIONS
- Descriptors DEC
- ARTERIES; BETA DECAY RADIOISOTOPES; BETA-PLUS DECAY RADIOISOTOPES; BLOOD VESSELS; BODY; CARDIOVASCULAR SYSTEM; CENTRAL NERVOUS SYSTEM; COMPUTERIZED TOMOGRAPHY; DIAGNOSTIC TECHNIQUES; DISEASES; DRUGS; EMISSION COMPUTED TOMOGRAPHY; FLUORINE ISOTOPES; FUNCTIONS; HOURS LIVING RADIOISOTOPES; ISOMERIC TRANSITION ISOTOPES; ISOTOPES; LABELLED COMPOUNDS; LIGHT NUCLEI; MATERIALS; MEMBRANE PROTEINS; NANOSECONDS LIVING RADIOISOTOPES; NERVOUS SYSTEM; NUCLEI; ODD-ODD NUCLEI; ORGANIC COMPOUNDS; ORGANS; PATHOLOGICAL CHANGES; PROCESSING; PROTEINS; RADIOACTIVE MATERIALS; RADIOISOTOPES; TOMOGRAPHY
Optional Information
- Notes
- Technology