Unveiling paths to Alzheimer's disease: excitation-inhibition ratio shapes hierarchical dynamics

Alzheimers disease is marked by cognitive and memory impairment, with early disruptions in the balance between excitatory and inhibitory neurotransmission, thought to be closely linked to co-occurrent brain changes. The posterior-to-anterior hypothesis posits that functional neurodegeneration begins in critical areas of the default mode network, particularly the hippocampus and posterior cingulate cortex, before extending to more anterior brain regions. This study seeks to evaluate how cortical hierarchy, measured with functional connectivity proxies for excitation/inhibition equilibrium, shapes across the continuum from cognitively unimpaired individuals to symptomatic Alzheimers disease. We include 97 participants: 28 patients (including 20 carriers of the Apolipoprotein E allele, {varepsilon}4+), 35 at-risk individuals ({varepsilon}4+), and 34 controls ({varepsilon}4-). Resting-state functional MRI and T1-weighted imaging were collected for all subjects, with a subset of Alzheimers patients also undergoing GABA-edited magnetic resonance spectroscopy in posterior cingulate cortex to provide a multimodal description of pathology-related excitation/inhibition disruptions impact on cortical hierarchical dynamics. To probe the validity of excitation/inhibition proxies, we (i) investigated the relationship between in-vivo measurements and cognitive profile in Alzheimers; (ii) compared default mode network temporal dynamics across groups; (iii) tested its multivariate association with cognitive profile and genetic interactions; (iv) and quantified subject fingerprints related to both pathology presence and genetic risk factors. The in-vivo excitation/inhibition ratio significantly related to cognitive deficits in Alzheimers patients, indicating that lower inhibition corresponds to poorer cognitive performance. A voxel-wise analysis demonstrated a positive association between neurometabolism in the posterior cingulate and temporal dynamics across default mode network regions, which can effectively differentiate between patients and controls. Furthermore, network fluctuations showed significant links to cognitive performance metrics, particularly among at-risk individuals. The study identified distinct functional fingerprints based on cortical temporal dynamics, emphasizing the interplay between genetic predisposition and the presence of Alzheimers disease. This investigation provides compelling evidence for the clinical importance of functional connectivity proxies related to excitation/inhibition, particularly within the default mode network. Neurodegeneration induces both a temporal and neurometabolic functional regression in higher-order cortical areas, resulting in a loss of specialized function. Consequently, the hierarchical continuum of cortical functions is disrupted, leading to a homogenization of brain activity. Excitation/inhibition proxies can expand our ability to recognize brain fingerprints of at-risk pre-symptomatic and pre-clinical subjects, opening pathways for potential disease-modifying treatments.