Literature DB >> 25698758

Brain amyloid-β burden is associated with disruption of intrinsic functional connectivity within the medial temporal lobe in cognitively normal elderly.

Zhuang Song1, Philip S Insel2, Shannon Buckley2, Seghel Yohannes3, Adam Mezher2, Alix Simonson2, Sarah Wilkins4, Duygu Tosun2, Susanne Mueller2, Joel H Kramer4, Bruce L Miller4, Michael W Weiner5.   

Abstract

The medial temporal lobe is implicated as a key brain region involved in the pathogenesis of Alzheimer's disease (AD) and consequent memory loss. Tau tangle aggregation in this region may develop concurrently with cortical Aβ deposition in preclinical AD, but the pathological relationship between tau and Aβ remains unclear. We used task-free fMRI with a focus on the medical temporal lobe, together with Aβ PET imaging, in cognitively normal elderly human participants. We found that cortical Aβ load was related to disrupted intrinsic functional connectivity of the perirhinal cortex, which is typically the first brain region affected by tauopathies in AD. There was no concurrent association of cortical Aβ load with cognitive performance or brain atrophy. These findings suggest that dysfunction in the medial temporal lobe may represent a very early sign of preclinical AD and may predict future memory loss.
Copyright © 2015 the authors 0270-6474/15/353240-08$15.00/0.

Entities:  

Keywords:  Alzheimer's disease; amyloid; hippocampus; perirhinal cortex

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Year:  2015        PMID: 25698758      PMCID: PMC4331637          DOI: 10.1523/JNEUROSCI.2092-14.2015

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


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