ePoster

GAIT-RELATED NEURAL SIGNATURE OF PRECLINICAL DEMENTIA RISK IN OLDER ADULTS

Denis Barbusseand 6 co-authors

Albert Einstein College of Medicine

FENS Forum 2026 (2026)
Barcelona, Spain
Board PS03-08AM-303

Presentation

Date TBA

Board: PS03-08AM-303

Poster preview

GAIT-RELATED NEURAL SIGNATURE OF PRECLINICAL DEMENTIA RISK IN OLDER ADULTS poster preview

Event Information

Poster Board

PS03-08AM-303

Abstract

Difficulties performing complex daily function (CdF) are a core diagnostic feature of dementia syndromes (De Sanctis et al., 2023; Verghese et al., 2023; Verghese et al., 2025). Yet the neural processes supporting CdF particularly during early stages of the dementia continuum remain unclear. We previously used a complex gait task to probe daily function in individuals as risk for mild cognitive impairment, showing that risk is associated with an anterior shift of fronto-parietal activation during complex gait (De Sanctis et al., 2023; De Sanctis et al., 2024).We are extending this framework to link blood-based Alzheimer’s pathology to gait-related EEG responses during walking. We have enrolled more than 150 community-dwelling older adults spanning a range of subclinical Alzheimer’s-related pathology quantified from blood using biomarker index (Meyer et al., 2024; Palmqvist et al., 2024; Coppinger et al., 2025). Participants walk on a treadmill with and without exposure to full-field optical flow perturbation designed to destabilize posture (De Sanctis et al., 2020). We test whether higher APS2 is associated with reduced central beta desynchronization and increased fronto-medial theta synchronization, and whether this neural pattern predicts cognition and CdF trajectories. Preliminary analyses suggest APS2-dependent differences in centro-frontal EEG activity. At the time of abstract submission, analyses are ongoing; final results will be presented at the FENS 2026 conference.

 Left panels show an illustration of the paradigm. Top panels show the mean scalp projection of two independent-component (IC) clusters localized to motor cortex (left column: left motor cortex cluster; right column: right motor cortex cluster). Each time–frequency panel displays the Walk with Optical Flow perturbation minus No Optical Flow perturbation contrast as a log power ratio computed after normalization to a common baseline (baseline window spanning the full gait cycle). Warm colors indicate higher power during Walk with Optical Flow perturbation than No Optical Flow perturbation, whereas cool colors indicate lower power during Walk with Optical Flow perturbation than No Optical Flow perturbation. The top row shows participants with high APS2, and the bottom row shows participants with low APS2. Frequency range is 3–45 Hz. Vertical lines mark the mean gait-event timings within the normalized gait cycle (RHS: Right Heel Strike, LTO: Left Toe Off, LHS: Left Heel Strike, RTO: Right ToeOff).

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