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Microglial activation in early Alzheimer trajectory is associated with higher grey matter volume

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Title: Microglial activation in early Alzheimer trajectory is associated with higher grey matter volume
Authors: Femminella, G
Dani, M
Wood, M
Fan, Z
Calsolaro, V
Atkinson, R
Edginton, T
Hinz, R
Brooks, D
Edison, P
Item Type: Journal Article
Abstract: Objective: To investigate the influence of microglial activation in the early stages of Alzheimer’s disease trajectory, we assessed the relationship between microglial activation and grey matter volume and hippocampal volume in MCI patients. Methods: In this study, fifty-five participants (37 early stages MCI and 18 controls) underwent [11C]PBR28 PET, a marker of microglial activation; volumetric MRI to evaluate grey matter and hippocampal volumes as well as clinical and neuropsychometric evaluation. [11C]PBR28 VT (volume of distribution) was calculated using arterial input function and Logan Graphical analysis. Grey matter volume and hippocampal volumes were calculated from MRI for each subject. Statistical parametric mapping software was used to perform voxel-wise correlations and biological parametric mapping analysis. Amyloid status was assessed using [18F]Flutemetamol PET. Results: Higher [11C]PBR28 VT in different cortical areas correlated with higher grey matter volume in both amyloid positive and negative MCI. Additionally, higher hippocampal volume correlated with higher cortical [11C]PBR28 Logan VT. Conclusions: In this in vivo study, we have demonstrated that microglial activation quantified using [11C]PBR28 PET was associated with higher grey matter volume and higher hippocampal volume in MCI patients. This may suggest that microglial activation may not always be associated with neuronal damage, and indeed it may have beneficial effect in early stages of Alzheimer’s trajectory. While further longitudinal studies are necessary, these findings have significant implications on therapeutic strategies targeting microglial activation.
Issue Date: 1-Mar-2019
Date of Acceptance: 14-Oct-2018
URI: http://hdl.handle.net/10044/1/65556
DOI: https://dx.doi.org/10.1212/WNL.0000000000007133
ISSN: 1526-632X
Publisher: American Academy of Neurology
Start Page: e1331
End Page: e1343
Journal / Book Title: Neurology
Volume: 92
Issue: 12
Copyright Statement: © 2019 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology. This is an open access article distributed under the terms of the Creative Commons Attribution License 4.0 (CC BY), which permits unrestricted use, distribution, and reproduction in anymedium, provided the original work is properly cited.
Sponsor/Funder: Alzheimer's Research UK (ARUK)
Medical Research Council (MRC)
Medical Research Council (MRC)
Funder's Grant Number: ART/PG2005/3
G84/6523
G1100810
Keywords: Science & Technology
Life Sciences & Biomedicine
Clinical Neurology
Neurosciences & Neurology
MILD COGNITIVE IMPAIRMENT
POSITRON-EMISSION-TOMOGRAPHY
PROTEIN 18 KDA
PARKINSONS-DISEASE
NEURONAL FUNCTION
MOUSE MODEL
BRAIN
NEUROINFLAMMATION
PET
INFLAMMATION
1103 Clinical Sciences
1109 Neurosciences
1702 Cognitive Sciences
Neurology & Neurosurgery
Publication Status: Published
Online Publication Date: 2019-02-22
Appears in Collections:Department of Medicine (up to 2019)