Bilateral subthalamic nucleus Deep Brain Stimulation (STN-DBS) and Levodopa-Carbidopa Intestinal Gel (LCIG) represent established treatment options for complicated Parkinson's disease (PD). Evidence regarding their effectiveness on axial symptoms remains limited, despite disability. This observational real-world cohort study included 317 PD patients who received STN-DBS (N = 203) or LCIG (N = 114) between 2005 and 2023 at two Italian centeres to compare their short- and long-term effects on axial symptoms. At baseline, LCIG group exhibited more severe axial and motor symptoms and higher prevalence of cognitive abnormalities than STN-DBS cohort. Longitudinally, LCIG treatment was associated with lower odds of long-term axial deterioration compared with STN-DBS, after adjustment for baseline differences and levodopa equivalent daily dose, despite an increased risk of dyskinesias. A significant treatment-by-time interaction suggested more favourable long-term axial symptom trajectories in the LCIG group.
STN-DBS and LCIG differentially affect long-term axial symptoms in Parkinson’s disease / F. Colucci, A.K.. - In: NPJ PARKINSON'S DISEASE. - ISSN 2373-8057. - (2026). [Epub ahead of print] [10.1038/s41531-026-01453-1]
STN-DBS and LCIG differentially affect long-term axial symptoms in Parkinson’s disease
R. Eleopra;
2026
Abstract
Bilateral subthalamic nucleus Deep Brain Stimulation (STN-DBS) and Levodopa-Carbidopa Intestinal Gel (LCIG) represent established treatment options for complicated Parkinson's disease (PD). Evidence regarding their effectiveness on axial symptoms remains limited, despite disability. This observational real-world cohort study included 317 PD patients who received STN-DBS (N = 203) or LCIG (N = 114) between 2005 and 2023 at two Italian centeres to compare their short- and long-term effects on axial symptoms. At baseline, LCIG group exhibited more severe axial and motor symptoms and higher prevalence of cognitive abnormalities than STN-DBS cohort. Longitudinally, LCIG treatment was associated with lower odds of long-term axial deterioration compared with STN-DBS, after adjustment for baseline differences and levodopa equivalent daily dose, despite an increased risk of dyskinesias. A significant treatment-by-time interaction suggested more favourable long-term axial symptom trajectories in the LCIG group.| File | Dimensione | Formato | |
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