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Abstract
Aim of the study was to evaluate possible associations between cognitive dysfunctions and development of Levodopa Induced Dyskinesia (LID). PD patients from the Parkinson’s disease Cognitive impairment Study cohort who underwent a baseline and follow-up neuropsychological evaluations were enrolled. Mild Cognitive Impairment (PD-MCI) was diagnosed according to MDS level II criteria. The following cognitive domains were evaluated: episodic memory, attention, executive function, visuo-spatial function and language. A domain was considered as impaired when the subject scored 2 standard deviation below normality cut-off values in at least one test for each domain. Levodopa equivalent dose, UPDRS-ME and LID were recorded at baseline and follow-up. To identify possible neuropsychological predictors associated with the probability of LID development at follow-up, Cox proportional-hazards regression model was used. Out of 139 PD patients enrolled (87 men, mean age 65.7 ± 9.4), 18 (12.9%) were dyskinetic at baseline. Out of 121 patients non-dyskinetic at baseline, 22 (18.1%) developed LID at follow-up. The impairment of the attention and executive domains strongly predicted the development of LID (HR 4.45;95%CI 1.49–13.23 and HR 3.46; 95%CI 1.26–9.48 respectively). Impairment of the attention and executive domains increased the risk of dyskinesia reflecting the alteration of common cortical network.
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1 University of Catania, Department of Medical, Surgical Sciences and Advanced Technologies, GF Ingrassia, Neurologic Unit, AOU “Policlinico-Vittorio Emanuele”, Catania, Italy (GRID:grid.8158.4) (ISNI:0000 0004 1757 1969)
2 University of Palermo, Department of Biomedicine, Neuroscience and Advanced Diagnostics, Palermo, Italy (GRID:grid.10776.37) (ISNI:0000 0004 1762 5517)
3 University of Palermo, Department of Sciences for Health Promotion and Mother-Child Care, Palermo, Italy (GRID:grid.10776.37) (ISNI:0000 0004 1762 5517)