Alexis Griggs, Giulia Carli, Taylor Brown, Prabesh Kanel, Stiven Roytman, Chatkaew Pongmala, Miriam van Emde Boas, Nicolaas I Bohnen
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引用次数: 0
Abstract
Objective: To investigate the cholinergic underpinnings of forward and retro-walking in individuals with Parkinson's disease (PD) using [18F]FEOBV PET, a radiotracer that binds to the vesicular acetylcholine transporter (VAChT).
Methods: We retrospectively included 44 patients with PD who underwent [18F]FEOBV PET imaging and forward- and retro-walking gait assessments. Voxel-wise correlation analyses were performed to examine associations between gait velocities and [18F]FEOBV binding, controlling for levodopa equivalent dose and disease duration. Linear regression and mediation analyses were then used to investigate the contribution of postural instability and gait disorder (PIGD) symptoms-measured using MDS-UPDRS items and the Mini-Balance Evaluation Systems Test (MiniBESTest)-as well as cognitive performance (attention, memory, executive, language, and visuospatial domains), to the observed associations.
Results: Slower retro-walking velocity was associated with lower [18F]FEOBV uptake in a subcortical-frontal-temporal cluster, including bilateral middle frontal cortex, anterior cingulate, insula, basal forebrain, and striatal regions. No significant associations were found for forward walking time. Linear regression analyses showed that MiniBESTest total scores, the reactive postural control subscore, and attention domain scores were associated with both cholinergic uptake in the identified cluster and retro-walking velocities. Mediation analyses revealed that attention and reactive postural control mediated the relationship between [18F]FEOBV binding and retro-walking performance.
Conclusions: Our findings indicate that retro-walking places greater demands on balance-particularly reactive postural control-and attentional resources than forward walking. Our results suggest that retro-walking might serve as part of an intervention strategy to improve balance and cognition in PD.