| Literature DB >> 32662517 |
Igor Fortel1, Laura E Korthauer2,3, Zachery Morrissey4, Liang Zhan5,6, Olusola Ajilore4, Ouri Wolfson7, Ira Driscoll2, Dan Schonfeld8, Alex Leow1,4.
Abstract
Synaptic dysfunction is hypothesized to be one of the earliest brain changes in Alzheimer's disease, leading to "hyperexcitability" in neuronal circuits. In this study, we evaluated a novel hyperexcitation indicator (HI) for each brain region using a hybrid resting-state structural connectome to probe connectome-level excitation-inhibition balance in cognitively intact middle-aged apolipoprotein E (APOE) ε4 carriers with noncarriers (16 male/22 female in each group). Regression with three-way interactions (sex, age, and APOE-ε4 carrier status) to assess the effect of APOE-ε4 on excitation-inhibition balance within each sex and across an age range of 40-60 years yielded a significant shift toward higher HI in female carriers compared with noncarriers (beginning at 50 years). Hyperexcitation was insignificant in the male group. Further, in female carriers the degree of hyperexcitation exhibited significant positive correlation with working memory performance (evaluated via a virtual Morris Water task) in three regions: the left pars triangularis, left hippocampus, and left isthmus of cingulate gyrus. Increased excitation of memory-related circuits may be evidence of compensatory recruitment of neuronal resources for memory-focused activities. In sum, our results are consistent with known Alzheimer's disease sex differences; in that female APOE-ε4 carriers have globally disrupted excitation-inhibition balance that may confer greater vulnerability to disease neuropathology.Entities:
Keywords: Alzheimer’s disease; Ising model; functional connectivity; hyperexcitation; multimodal biomarkers
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Year: 2020 PMID: 32662517 PMCID: PMC7609923 DOI: 10.1093/cercor/bhaa190
Source DB: PubMed Journal: Cereb Cortex ISSN: 1047-3211 Impact factor: 4.861