Connectome Signatures of Hyperexcitation in Cognitively Intact Middle-Aged Female APOE-ε4 Carriers. (14th July 2020)

• Record Type: Journal Article
• Authors: Fortel, Igor; Korthauer, Laura E; Morrissey, Zachery; Zhan, Liang; Ajilore, Olusola; Wolfson, Ouri; Driscoll, Ira; Schonfeld, Dan; Leow, Alex
• Is Part Of: Cerebral cortex. Volume 30:Number 12(2020)
• Page Start: 6350
• Page End: 6362
• Publication Date: 2020-07-14
• Subjects: Alzheimer's disease -- functional connectivity -- Ising model -- multimodal biomarkers -- hyperexcitation; Cerebral cortex -- Periodicals; Brain -- Periodicals; 612.825
• DOI: 10.1093/cercor/bhaa190
• Languages: English
• ISSNs: 1047-3211

Abstract

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.