Does inflammation precede tau aggregation in early Alzheimer's disease? A PET study
Objective: Our aim was to assess with positron emission tomography (PET) the temporal and spatial inter-relationships between levels of cortical microglial activation and the aggregated amyloid-β and tau load in mild cognitive impairment (MCI) and early Alzheimer's disease (AD). Methods: Six cl...
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Published in | Neurobiology of disease Vol. 117; pp. 211 - 216 |
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Main Authors | , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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United States
Elsevier Inc
01.09.2018
Elsevier |
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Abstract | Objective: Our aim was to assess with positron emission tomography (PET) the temporal and spatial inter-relationships between levels of cortical microglial activation and the aggregated amyloid-β and tau load in mild cognitive impairment (MCI) and early Alzheimer's disease (AD).
Methods: Six clinically probable AD and 20 MCI subjects had inflammation (11C-(R)-PK11195), amyloid (11C-PiB) and tau (18F-flortaucipir) PET, magnetic resonance imaging (MRI) and a neuropsychological assessment. Parametric images of tracer binding were interrogated at a voxel level and by region of interest analyses.
Results: 55% of MCI and 83% of AD subjects had a high amyloid-β load. We have previously reported that clusters of correlated amyloid and inflammation levels are present in cortex. Here we found no correlation between levels of inflammation (11C-(R)-PK11195 BPND) and tau (18F-flortaucipir SUVR) or MMSE scores in high amyloid-β cases.
Interpretation: While correlated levels of amyloid-β and inflammation can be seen in MCI, we did not detect an association between levels of cortical tau tangles and inflammation in our series of high amyloid-β cases. High levels of inflammation could be seen in amyloid-β positive MCI cases where 18F-flortaucipir signals were low suggesting microglial activation precedes tau tangle formation. Inflammation levels were higher in high amyloid-β MCI than in early AD cases, compatible with it initially playing a protective role.
•Microglial activation is an early event in Alzheimer's disease neuropathology.•Inflammation can be seen in prodromal AD in the absence of detectable tau deposition.•Early inflammation may initially be a protective mechanism that subsequently fails. |
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AbstractList | Objective: Our aim was to assess with positron emission tomography (PET) the temporal and spatial inter-relationships between levels of cortical microglial activation and the aggregated amyloid-β and tau load in mild cognitive impairment (MCI) and early Alzheimer's disease (AD).Methods: Six clinically probable AD and 20 MCI subjects had inflammation (11C-(R)-PK11195), amyloid (11C-PiB) and tau (18F-flortaucipir) PET, magnetic resonance imaging (MRI) and a neuropsychological assessment. Parametric images of tracer binding were interrogated at a voxel level and by region of interest analyses.Results: 55% of MCI and 83% of AD subjects had a high amyloid-β load. We have previously reported that clusters of correlated amyloid and inflammation levels are present in cortex. Here we found no correlation between levels of inflammation (11C-(R)-PK11195 BPND) and tau (18F-flortaucipir SUVR) or MMSE scores in high amyloid-β cases.Interpretation: While correlated levels of amyloid-β and inflammation can be seen in MCI, we did not detect an association between levels of cortical tau tangles and inflammation in our series of high amyloid-β cases. High levels of inflammation could be seen in amyloid-β positive MCI cases where 18F-flortaucipir signals were low suggesting microglial activation precedes tau tangle formation. Inflammation levels were higher in high amyloid-β MCI than in early AD cases, compatible with it initially playing a protective role. Objective: Our aim was to assess with positron emission tomography (PET) the temporal and spatial inter-relationships between levels of cortical microglial activation and the aggregated amyloid-β and tau load in mild cognitive impairment (MCI) and early Alzheimer's disease (AD). Methods: Six clinically probable AD and 20 MCI subjects had inflammation (11C-(R)-PK11195), amyloid (11C-PiB) and tau (18F-flortaucipir) PET, magnetic resonance imaging (MRI) and a neuropsychological assessment. Parametric images of tracer binding were interrogated at a voxel level and by region of interest analyses. Results: 55% of MCI and 83% of AD subjects had a high amyloid-β load. We have previously reported that clusters of correlated amyloid and inflammation levels are present in cortex. Here we found no correlation between levels of inflammation (11C-(R)-PK11195 BPND) and tau (18F-flortaucipir SUVR) or MMSE scores in high amyloid-β cases. Interpretation: While correlated levels of amyloid-β and inflammation can be seen in MCI, we did not detect an association between levels of cortical tau tangles and inflammation in our series of high amyloid-β cases. High levels of inflammation could be seen in amyloid-β positive MCI cases where 18F-flortaucipir signals were low suggesting microglial activation precedes tau tangle formation. Inflammation levels were higher in high amyloid-β MCI than in early AD cases, compatible with it initially playing a protective role. •Microglial activation is an early event in Alzheimer's disease neuropathology.•Inflammation can be seen in prodromal AD in the absence of detectable tau deposition.•Early inflammation may initially be a protective mechanism that subsequently fails. Our aim was to assess with positron emission tomography (PET) the temporal and spatial inter-relationships between levels of cortical microglial activation and the aggregated amyloid-β and tau load in mild cognitive impairment (MCI) and early Alzheimer's disease (AD).OBJECTIVEOur aim was to assess with positron emission tomography (PET) the temporal and spatial inter-relationships between levels of cortical microglial activation and the aggregated amyloid-β and tau load in mild cognitive impairment (MCI) and early Alzheimer's disease (AD).Six clinically probable AD and 20 MCI subjects had inflammation (11C-(R)-PK11195), amyloid (11C-PiB) and tau (18F-flortaucipir) PET, magnetic resonance imaging (MRI) and a neuropsychological assessment. Parametric images of tracer binding were interrogated at a voxel level and by region of interest analyses.METHODSSix clinically probable AD and 20 MCI subjects had inflammation (11C-(R)-PK11195), amyloid (11C-PiB) and tau (18F-flortaucipir) PET, magnetic resonance imaging (MRI) and a neuropsychological assessment. Parametric images of tracer binding were interrogated at a voxel level and by region of interest analyses.55% of MCI and 83% of AD subjects had a high amyloid-β load. We have previously reported that clusters of correlated amyloid and inflammation levels are present in cortex. Here we found no correlation between levels of inflammation (11C-(R)-PK11195 BPND) and tau (18F-flortaucipir SUVR) or MMSE scores in high amyloid-β cases.RESULTS55% of MCI and 83% of AD subjects had a high amyloid-β load. We have previously reported that clusters of correlated amyloid and inflammation levels are present in cortex. Here we found no correlation between levels of inflammation (11C-(R)-PK11195 BPND) and tau (18F-flortaucipir SUVR) or MMSE scores in high amyloid-β cases.While correlated levels of amyloid-β and inflammation can be seen in MCI, we did not detect an association between levels of cortical tau tangles and inflammation in our series of high amyloid-β cases. High levels of inflammation could be seen in amyloid-β positive MCI cases where 18F-flortaucipir signals were low suggesting microglial activation precedes tau tangle formation. Inflammation levels were higher in high amyloid-β MCI than in early AD cases, compatible with it initially playing a protective role.INTERPRETATIONWhile correlated levels of amyloid-β and inflammation can be seen in MCI, we did not detect an association between levels of cortical tau tangles and inflammation in our series of high amyloid-β cases. High levels of inflammation could be seen in amyloid-β positive MCI cases where 18F-flortaucipir signals were low suggesting microglial activation precedes tau tangle formation. Inflammation levels were higher in high amyloid-β MCI than in early AD cases, compatible with it initially playing a protective role. Our aim was to assess with positron emission tomography (PET) the temporal and spatial inter-relationships between levels of cortical microglial activation and the aggregated amyloid-β and tau load in mild cognitive impairment (MCI) and early Alzheimer's disease (AD). Six clinically probable AD and 20 MCI subjects had inflammation ( C-(R)-PK11195), amyloid ( C-PiB) and tau ( F-flortaucipir) PET, magnetic resonance imaging (MRI) and a neuropsychological assessment. Parametric images of tracer binding were interrogated at a voxel level and by region of interest analyses. 55% of MCI and 83% of AD subjects had a high amyloid-β load. We have previously reported that clusters of correlated amyloid and inflammation levels are present in cortex. Here we found no correlation between levels of inflammation ( C-(R)-PK11195 BP ) and tau ( F-flortaucipir SUVR) or MMSE scores in high amyloid-β cases. While correlated levels of amyloid-β and inflammation can be seen in MCI, we did not detect an association between levels of cortical tau tangles and inflammation in our series of high amyloid-β cases. High levels of inflammation could be seen in amyloid-β positive MCI cases where F-flortaucipir signals were low suggesting microglial activation precedes tau tangle formation. Inflammation levels were higher in high amyloid-β MCI than in early AD cases, compatible with it initially playing a protective role. |
Author | Eskildsen, Simon F. Hinz, Rainer Brændgaard, Hans Borghammer, Per Sommerauer, Michael Aanerud, Joel Hansen, Allan K. Hansen, Kim V. Brooks, David J. Gottrup, Hanne Parbo, Peter Amidi, Ali Ismail, Rola Stokholm, Morten G. Schaldemose, Jeppe L. |
Author_xml | – sequence: 1 givenname: Peter surname: Parbo fullname: Parbo, Peter email: peter.parbo@clin.au.dk organization: Department of Nuclear Medicine and PET Centre, Aarhus University Hospital, Aarhus, Denmark – sequence: 2 givenname: Rola surname: Ismail fullname: Ismail, Rola organization: Department of Nuclear Medicine and PET Centre, Aarhus University Hospital, Aarhus, Denmark – sequence: 3 givenname: Michael surname: Sommerauer fullname: Sommerauer, Michael organization: Department of Nuclear Medicine and PET Centre, Aarhus University Hospital, Aarhus, Denmark – sequence: 4 givenname: Morten G. surname: Stokholm fullname: Stokholm, Morten G. organization: Department of Nuclear Medicine and PET Centre, Aarhus University Hospital, Aarhus, Denmark – sequence: 5 givenname: Allan K. surname: Hansen fullname: Hansen, Allan K. organization: Department of Nuclear Medicine and PET Centre, Aarhus University Hospital, Aarhus, Denmark – sequence: 6 givenname: Kim V. surname: Hansen fullname: Hansen, Kim V. organization: Department of Nuclear Medicine and PET Centre, Aarhus University Hospital, Aarhus, Denmark – sequence: 7 givenname: Ali surname: Amidi fullname: Amidi, Ali organization: Department of Psychology and Behavioural Sciences, Department of Oncology, Aarhus University & Aarhus University Hospital, Denmark – sequence: 8 givenname: Jeppe L. surname: Schaldemose fullname: Schaldemose, Jeppe L. organization: Department of Nuclear Medicine and PET Centre, Aarhus University Hospital, Aarhus, Denmark – sequence: 9 givenname: Hanne surname: Gottrup fullname: Gottrup, Hanne organization: Department of Neurology, Aarhus University Hospital, Aarhus, Denmark – sequence: 10 givenname: Hans surname: Brændgaard fullname: Brændgaard, Hans organization: Department of Neurology, Aarhus University Hospital, Aarhus, Denmark – sequence: 11 givenname: Simon F. surname: Eskildsen fullname: Eskildsen, Simon F. organization: Center of Functionally Integrative Neuroscience (CFIN), Aarhus University, Aarhus, Denmark – sequence: 12 givenname: Per surname: Borghammer fullname: Borghammer, Per organization: Department of Nuclear Medicine and PET Centre, Aarhus University Hospital, Aarhus, Denmark – sequence: 13 givenname: Rainer surname: Hinz fullname: Hinz, Rainer organization: Wolfson Molecular Imaging Centre, University of Manchester, Manchester, UK – sequence: 14 givenname: Joel surname: Aanerud fullname: Aanerud, Joel organization: Department of Nuclear Medicine and PET Centre, Aarhus University Hospital, Aarhus, Denmark – sequence: 15 givenname: David J. surname: Brooks fullname: Brooks, David J. organization: Department of Nuclear Medicine and PET Centre, Aarhus University Hospital, Aarhus, Denmark |
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Keywords | PK11195 PiB ROI Aβ flortaucipir SPM Amyloid PET Tau PET MMSE SUVR BPND Alzheimer's disease Positron emission tomography Microglial activation BPM |
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Snippet | Objective: Our aim was to assess with positron emission tomography (PET) the temporal and spatial inter-relationships between levels of cortical microglial... Our aim was to assess with positron emission tomography (PET) the temporal and spatial inter-relationships between levels of cortical microglial activation and... |
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SubjectTerms | Aged Aged, 80 and over Alzheimer Disease - diagnostic imaging Alzheimer Disease - metabolism Alzheimer's disease Amyloid PET Cognitive Dysfunction - diagnostic imaging Cognitive Dysfunction - metabolism Cross-Sectional Studies Early Diagnosis Female Humans Inflammation - diagnostic imaging Inflammation - metabolism Male Microglial activation Middle Aged Positron emission tomography Positron-Emission Tomography - methods Protein Aggregation, Pathological - diagnostic imaging Protein Aggregation, Pathological - metabolism Tau PET tau Proteins - metabolism |
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Title | Does inflammation precede tau aggregation in early Alzheimer's disease? A PET study |
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