Subthalamic functional connectivity associated with freezing of gait dopa-response

• Published in: Parkinsonism & related disorders Vol. 118; p. 105952
• Main Authors: Lench, Daniel H, Doolittle, Jade D, Ramakrishnan, Viswanathan, Rowland, Nathan, Revuelta, Gonzalo J
• Format: Journal Article
• Language: English
• Published: England 01.01.2024
• Subjects: Deep Brain Stimulation; Gait - physiology; Gait Disorders, Neurologic - diagnostic imaging; Gait Disorders, Neurologic - drug therapy; Gait Disorders, Neurologic - etiology; Humans; Levodopa - pharmacology; Levodopa - therapeutic use; Parkinson Disease - complications; Parkinson Disease - diagnostic imaging; Parkinson Disease - drug therapy; Connectivity; Dopamine; Parkinson's disease; Gait; Freezing
• ISSN: 1353-8020; 1873-5126
• DOI: 10.1016/j.parkreldis.2023.105952

Freezing of gait (FOG) is a prevalent and debilitating feature of Parkinson's Disease (PD). The subthalamic nucleus (STN) is a center for controlled locomotion and a common DBS target. The objective of this study was to identify STN circuitry associated with FOG response to dopaminergic medication. In this study, we compare BOLD functional connectivity of the subthalamic nucleus (STN) in participants with and without dopa-responsive FOG. 55 PD participants either with FOG (n = 38) or without FOG (n = 17) were recruited. Among FOG participants 22 were dopa-responsive and 16 were dopa-unresponsive. STN whole-brain connectivity was performed using CONN toolbox. The relationship between the degree of self-reported FOG dopa-response and STN connectivity was evaluated using partial correlations corrected for age, disease duration, and levodopa equivalent daily dose. Right STN connectivity with the cerebellar locomotor region and the temporal/occipital cortex was greater in the dopa-responsive FOG group (voxel threshold p < 0.01, FWE corrected p < 0.05). Left STN connectivity with the occipital cortex was greater in the dopa-responsive FOG group and connectivity with the postcentral gyrus was greater in the dopa-unresponsive FOG group. Strength of connectivity to these regions correlated with l-dopa induced improvement in UPDRS Item-14 (FOG), but not UPDRS Part-III (overall motor score). We demonstrate that dopa-unresponsive FOG is associated with changes in BOLD functional connectivity between the STN and locomotor as well as sensory processing regions. This finding supports the conceptual framework that effective treatment for freezing of gait likely requires the engagement of both locomotor and sensory brain regions.