Effective connectivity in the default mode network is distinctively disrupted in Alzheimer's disease—A simultaneous resting‐state FDG‐PET/fMRI study

A prominent finding of postmortem and molecular imaging studies on Alzheimer's disease (AD) is the accumulation of neuropathological proteins in brain regions of the default mode network (DMN). Molecular models suggest that the progression of disease proteins depends on the directionality of si...

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Published inHuman brain mapping Vol. 42; no. 13; pp. 4134 - 4143
Main Authors Scherr, Martin, Utz, Lukas, Tahmasian, Masoud, Pasquini, Lorenzo, Grothe, Michel J., Rauschecker, Josef P., Grimmer, Timo, Drzezga, Alexander, Sorg, Christian, Riedl, Valentin
Format Journal Article
LanguageEnglish
Published Hoboken, USA John Wiley & Sons, Inc 01.09.2021
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Summary:A prominent finding of postmortem and molecular imaging studies on Alzheimer's disease (AD) is the accumulation of neuropathological proteins in brain regions of the default mode network (DMN). Molecular models suggest that the progression of disease proteins depends on the directionality of signaling pathways. At network level, effective connectivity (EC) reflects directionality of signaling pathways. We hypothesized a specific pattern of EC in the DMN of patients with AD, related to cognitive impairment. Metabolic connectivity mapping is a novel measure of EC identifying regions of signaling input based on neuroenergetics. We simultaneously acquired resting‐state functional MRI and FDG‐PET data from patients with early AD (n = 35) and healthy subjects (n = 18) on an integrated PET/MR scanner. We identified two distinct subnetworks of EC in the DMN of healthy subjects: an anterior part with bidirectional EC between hippocampus and medial prefrontal cortex and a posterior part with predominant input into medial parietal cortex. Patients had reduced input into the medial parietal system and absent input from hippocampus into medial prefrontal cortex (p < 0.05, corrected). In a multiple linear regression with unimodal imaging and EC measures (F4,25 = 5.63, p = 0.002, r2 = 0.47), we found that EC (β = 0.45, p = 0.012) was stronger associated with cognitive deficits in patients than any of the PET and fMRI measures alone. Our approach indicates specific disruptions of EC in the DMN of patients with AD and might be suitable to test molecular theories about downstream and upstream spreading of neuropathology in AD.
Bibliography:Funding information
Bundesministerium für Bildung und Forschung, Grant/Award Number: 01EV0710; Deutsche Forschungsgemeinschaft, Grant/Award Number: 273427765; German Research Foundation, Grant/Award Number: 273427765; European Union Seventh Framework Programme, Grant/Award Number: n 291763; Technische Universität Muenchen—Institute for Advanced Study; Federal Ministry of Education and Science, Grant/Award Number: BMBF 01EV0710
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Martin Scherr, Lukas Utz, Christian Sorg, and Valentin Riedl authors contributed equally to this study.
Funding information Bundesministerium für Bildung und Forschung, Grant/Award Number: 01EV0710; Deutsche Forschungsgemeinschaft, Grant/Award Number: 273427765; German Research Foundation, Grant/Award Number: 273427765; European Union Seventh Framework Programme, Grant/Award Number: n 291763; Technische Universität Muenchen—Institute for Advanced Study; Federal Ministry of Education and Science, Grant/Award Number: BMBF 01EV0710
ISSN:1065-9471
1097-0193
1097-0193
DOI:10.1002/hbm.24517