| Literature DB >> 25405944 |
Jeremy A Elman1, Cindee M Madison2, Suzanne L Baker1, Jacob W Vogel2, Shawn M Marks2, Sam Crowley1, James P O'Neil1, William J Jagust3.
Abstract
Beta-amyloid (Aβ) deposition is one of the hallmarks of Alzheimer's disease (AD). However, it is also present in some cognitively normal elderly adults and may represent a preclinical disease state. While AD patients exhibit disrupted functional connectivity (FC) both within and between resting-state networks, studies of preclinical cases have focused primarily on the default mode network (DMN). The extent to which Aβ-related effects occur outside of the DMN and between networks remains unclear. In the present study, we examine how within- and between-network FC are related to both global and regional Aβ deposition as measured by [(11)C]PIB-PET in 92 cognitively normal older people. We found that within-network FC changes occurred in multiple networks, including the DMN. Changes of between-network FC were also apparent, suggesting that regions maintaining connections to multiple networks may be particularly susceptible to Aβ-induced alterations. Cortical regions showing altered FC clustered in parietal and temporal cortex, areas known to be susceptible to AD pathology. These results likely represent a mix of local network disruption, compensatory reorganization, and impaired control network function. They indicate the presence of Aβ-related dysfunction of neural systems in cognitively normal people well before these areas become hypometabolic with the onset of cognitive decline.Entities:
Keywords: PIB-PET; aging; beta-amyloid; functional connectivity; resting-state fMRI
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Year: 2014 PMID: 25405944 PMCID: PMC4712800 DOI: 10.1093/cercor/bhu259
Source DB: PubMed Journal: Cereb Cortex ISSN: 1047-3211 Impact factor: 5.357