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Alterations in resting-state network dynamics along the Alzheimer’s disease continuum: a combined MEG-PET/MR approach

D. Puttaert, N. Coquelet, V. Wens, P. Peigneux, P. Fery, A. Rovai, N. Trotta, J-C. Bier, S. Goldman, X. De Tiège
doi: https://doi.org/10.1101/2020.05.18.101683
D. Puttaert
1Laboratoire de Cartographie fonctionnelle du Cerveau (LCFC), UNI – ULB Neuroscience Institute, Université libre de Bruxelles (ULB), Brussels, Belgium
3Neuropsychology and Functional Neuroimaging Research Unit (UR2NF), Center for Research in Cognition and Neurosciences (CRCN), UNI – ULB Neuroscience Institute, Université libre de Bruxelles (ULB), Brussels, Belgium
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  • For correspondence: delphine.puttaert@ulb.ac.be
N. Coquelet
1Laboratoire de Cartographie fonctionnelle du Cerveau (LCFC), UNI – ULB Neuroscience Institute, Université libre de Bruxelles (ULB), Brussels, Belgium
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V. Wens
1Laboratoire de Cartographie fonctionnelle du Cerveau (LCFC), UNI – ULB Neuroscience Institute, Université libre de Bruxelles (ULB), Brussels, Belgium
2Department of Functional Neuroimaging, Service of Nuclear Medicine, CUB Hôpital Erasme, Université libre de Bruxelles (ULB), Brussels, Belgium
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P. Peigneux
3Neuropsychology and Functional Neuroimaging Research Unit (UR2NF), Center for Research in Cognition and Neurosciences (CRCN), UNI – ULB Neuroscience Institute, Université libre de Bruxelles (ULB), Brussels, Belgium
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P. Fery
3Neuropsychology and Functional Neuroimaging Research Unit (UR2NF), Center for Research in Cognition and Neurosciences (CRCN), UNI – ULB Neuroscience Institute, Université libre de Bruxelles (ULB), Brussels, Belgium
4Service of Neuropsychology and Speech Therapy, CUB Hôpital Erasme, Université libre de Bruxelles (ULB), Brussels, Belgium
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A. Rovai
1Laboratoire de Cartographie fonctionnelle du Cerveau (LCFC), UNI – ULB Neuroscience Institute, Université libre de Bruxelles (ULB), Brussels, Belgium
2Department of Functional Neuroimaging, Service of Nuclear Medicine, CUB Hôpital Erasme, Université libre de Bruxelles (ULB), Brussels, Belgium
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N. Trotta
1Laboratoire de Cartographie fonctionnelle du Cerveau (LCFC), UNI – ULB Neuroscience Institute, Université libre de Bruxelles (ULB), Brussels, Belgium
2Department of Functional Neuroimaging, Service of Nuclear Medicine, CUB Hôpital Erasme, Université libre de Bruxelles (ULB), Brussels, Belgium
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J-C. Bier
5Department of Neurology, CUB Hôpital Erasme, Université libre de Bruxelles (ULB), Brussels, Belgium
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S. Goldman
1Laboratoire de Cartographie fonctionnelle du Cerveau (LCFC), UNI – ULB Neuroscience Institute, Université libre de Bruxelles (ULB), Brussels, Belgium
2Department of Functional Neuroimaging, Service of Nuclear Medicine, CUB Hôpital Erasme, Université libre de Bruxelles (ULB), Brussels, Belgium
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X. De Tiège
1Laboratoire de Cartographie fonctionnelle du Cerveau (LCFC), UNI – ULB Neuroscience Institute, Université libre de Bruxelles (ULB), Brussels, Belgium
2Department of Functional Neuroimaging, Service of Nuclear Medicine, CUB Hôpital Erasme, Université libre de Bruxelles (ULB), Brussels, Belgium
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Abstract

Human brain activity is intrinsically organized into resting-state networks (RSNs) that transiently activate or deactivate at the sub-second timescale. Few neuroimaging studies have addressed how Alzheimer’s disease (AD) affects these fast temporal brain dynamics, and how they relate to the cognitive, structural and metabolic abnormalities characterizing AD.

We aimed at closing this gap by investigating both brain structure and function using magnetoencephalography (MEG) and hybrid positron emission tomography-magnetic resonance (PET/MR) in 10 healthy elders, 10 patients with Subjective Cognitive Decline (SCD), 10 patients with amnestic Mild Cognitive Impairment (aMCI) and 10 patients with typical Alzheimer’s disease with dementia (AD). The fast activation/deactivation state dynamics of RSNs were assessed using hidden Markov modeling (HMM) of power envelope fluctuations at rest measured with MEG. HMM patterns were related to participants’ cognitive test scores, whole hippocampal grey matter volume and regional brain glucose metabolism.

The posterior default-mode network (DMN) was less often activated and for shorter durations in AD patients than matched healthy elders. No significant difference was found in patients with SCD or aMCI. The time spent by participants in the activated posterior DMN state did not correlate significantly with cognitive scores. However, it correlated positively with the whole hippocampal volume and regional glucose consumption in the right temporo-parietal junctions and dorsolateral prefrontal cortex, and negatively with glucose consumption in the cerebellum.

In AD patients, alterations of posterior DMN power activation dynamics at rest correlate with structural and neurometabolic abnormalities. These findings represent an additional electrophysiological correlate of AD-related synaptic and neural dysfunction.

Competing Interest Statement

The authors have declared no competing interest.

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The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. All rights reserved. No reuse allowed without permission.
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Posted May 20, 2020.
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Alterations in resting-state network dynamics along the Alzheimer’s disease continuum: a combined MEG-PET/MR approach
D. Puttaert, N. Coquelet, V. Wens, P. Peigneux, P. Fery, A. Rovai, N. Trotta, J-C. Bier, S. Goldman, X. De Tiège
bioRxiv 2020.05.18.101683; doi: https://doi.org/10.1101/2020.05.18.101683
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Alterations in resting-state network dynamics along the Alzheimer’s disease continuum: a combined MEG-PET/MR approach
D. Puttaert, N. Coquelet, V. Wens, P. Peigneux, P. Fery, A. Rovai, N. Trotta, J-C. Bier, S. Goldman, X. De Tiège
bioRxiv 2020.05.18.101683; doi: https://doi.org/10.1101/2020.05.18.101683

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