ArticleCNS neuroscience & therapeutics2025
Identifying Risk Factors and Constructing Predictive Models for Wearing-Off and Dyskinesia in Chinese Patients With Parkinson's Disease on Long-Term Levodopa Therapy.
Article in CNS neuroscience & therapeutics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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Who cites it
3 citing papers in PubMed.
- Association of Reproductive Factors and Postmenopausal Sex Hormones With Cognitive Impairment in Postmenopausal Women With Parkinson's Disease.CNS neuroscience & therapeutics · 2026Article
- Neuroprotective Effects of Lycopene in Parkinson's Disease Mice: Potential Modulation of DAT/SLC6A3-Mediated Dopaminergic Pathway.Nutrients · 2026Article
- Identifying Risk Factors and Constructing Predictive Models for Wearing-Off and Dyskinesia in Chinese Patients With Parkinson's Disease on Long-Term Levodopa Therapy.CNS neuroscience & therapeutics · 2025Article
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11 authors.
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Abstract
aimsThis study aimed to investigate the incidence and risk factors of motor complications including wearing-off (WO) and dyskinesia during long-term levodopa (LD) therapy in Chinese patients with Parkinson's disease (PD), and develop corresponding predictive models, thereby providing a basis for personalized treatment strategies.
methodsThis cross-sectional study included 208 consecutive PD patients who were recruited. The presence of WO and dyskinesia was assessed by a 9-item wearing-off questionnaire and the Unified Parkinson's Disease Rating Scale part IV. Univariate and multivariate logistic regression analyses were used to predict the risk factors of WO and dyskinesia. Predictive models for WO and dyskinesia were then constructed, and their diagnostic performance was evaluated using the area under the curve (AUC).
resultsThe overall prevalence rate of motor complications was 46.2% (96/208), with a prevalence of 45.7% (95/208) for WO, 22.1% (46/208) for dyskinesia, and 21.6% (45/208) for the simultaneous occurrence of WO and dyskinesia. Younger age at onset (OR 0.92, p < 0.001), higher levodopa-equivalent daily dose (LEDD) (OR 1.00, p < 0.001), and higher Hoehn-Yahr stage (OR 3.41, p < 0.001) were independent risk factors for WO. A predictive model for WO constructed using these three variables demonstrated high diagnostic efficacy with an AUC of 0.887 (95% CI 0.842-0.932), a sensitivity of 84%, and a specificity of 83%. The independent risk factors for dyskinesia included younger age at onset (OR 0.94, p < 0.001), akinetic-rigid type (OR 2.42, p = 0.034), and higher LEDD (OR 1.01, p < 0.001). A predictive model for dyskinesia constructed using these three variables yielded an AUC value of 0.829 (95% CI 0.767-0.897), with a sensitivity of 67% and a specificity of 89%. The two models were both well calibrated and had a high net clinical benefit.
conclusionOur findings suggest that the prevalence of motor complications during long-term LD treatment is relatively high among PD patients in China, with WO occurring more commonly than dyskinesia. Younger age at PD onset, higher LEDD, more severe disease, and akinetic-rigid subtype are key predictors of motor complications. The predictive models developed in this study could serve as a potential tool to assist clinicians in identifying patients at higher risk for WO and dyskinesia, and may support personalized treatment optimization.
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