Author
Listed:
- Theresa M. Harrison
(Helen Wills Neuroscience Institute, UC Berkeley)
- Anne Maass
(Helen Wills Neuroscience Institute, UC Berkeley
German Center for Neurodegenerative Diseases)
- Jenna N. Adams
(Helen Wills Neuroscience Institute, UC Berkeley)
- Richard Du
(Helen Wills Neuroscience Institute, UC Berkeley)
- Suzanne L. Baker
(Lawrence Berkeley National Laboratory)
- William J. Jagust
(Helen Wills Neuroscience Institute, UC Berkeley
Lawrence Berkeley National Laboratory)
Abstract
The tau protein aggregates in aging and Alzheimer disease and may lead to memory loss through disruption of medial temporal lobe (MTL)-dependent memory systems. Here, we investigated tau-mediated mechanisms of hippocampal dysfunction that underlie the expression of episodic memory decline using fMRI measures of hippocampal local coherence (regional homogeneity; ReHo), distant functional connectivity and tau-PET. We show that age and tau pathology are related to higher hippocampal ReHo. Functional disconnection between the hippocampus and other components of the MTL memory system, particularly an anterior-temporal network specialized for object memory, is also associated with higher hippocampal ReHo and greater tau burden in anterior-temporal regions. These associations are not observed in the posteromedial network, specialized for context/spatial information. Higher hippocampal ReHo predicts worse memory performance. These findings suggest that tau pathology plays a role in disconnecting the hippocampus from specific MTL memory systems leading to increased local coherence and memory decline.
Suggested Citation
Theresa M. Harrison & Anne Maass & Jenna N. Adams & Richard Du & Suzanne L. Baker & William J. Jagust, 2019.
"Tau deposition is associated with functional isolation of the hippocampus in aging,"
Nature Communications, Nature, vol. 10(1), pages 1-12, December.
Handle:
RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-019-12921-z
DOI: 10.1038/s41467-019-12921-z
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