4.4 Article

Axial Impairment Following Deep Brain Stimulation in Parkinson's Disease: A Surgicogenomic Approach

Journal

JOURNAL OF PARKINSONS DISEASE
Volume 12, Issue 1, Pages 117-128

Publisher

IOS PRESS
DOI: 10.3233/JPD-212730

Keywords

Parkinson's disease; deep brain stimulation; gait apraxia; postural instability; genotyping

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The study aimed to identify genetic variants associated with clinical heterogeneity in DBS outcome of PD patients, with the potential to improve patient selection for DBS surgery. The findings suggest a genetic underpinning to the response to surgical intervention, particularly with respect to axial motor improvement.
Background: Postoperative outcome following deep brain stimulation (DBS) of the subthalamic nucleus is variable, particularly with respect to axial motor improvement. We hypothesized a genetic underpinning to the response to surgical intervention, termed surgicogenomics. Objective: We aimed to identify genetic variants associated with clinical heterogeneity in DBS outcome of Parkinson's disease (PD) patients that could then be applied clinically to target selection leading to improved surgical outcome. Methods: Retrospective clinical data was extracted from 150 patient's charts. Each individual was genotyped using the genome-wide NeuroX array tailored to study neurologic diseases. Genetic data were clustered based on surgical outcome assessed by comparing pre- and post-operative scores of levodopa equivalent daily dose and axial impairment at one and five years post-surgery. Allele frequencies were compared between patients with excellent vs. moderate/poor outcomes grouped using a priori defined cut-offs. We analyzed common variants, burden of rare coding variants, and PD polygenic risk score. Results: NeuroX identified 2,917 polymorphic markers at 113 genes mapped to known PD loci. The gene-burden analyses of 202 rare nonsynonymous variants suggested a nominal association of axial impairment with 14 genes (most consistent with CRHR1, IP6K2, and PRSS3). The strongest association with surgical outcome was detected between a reduction in levodopa equivalent daily dose and common variations tagging two linkage disequilibrium blocks with SH3GL2. Conclusion: Once validated in independent populations, our findings may be implemented to improve patient selection for DBS in PD.

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