Department of Medical, Surgical Sciences and Advanced Technologies, GF Ingrassia, Neurologic Unit, AOU "Policlinico-Vittorio Emanuele", University of Catania, Via Santa Sofia n.78, 95100, Catania, Sicily, Italy.
Department of Biomedicine, Neuroscience and Advanced Diagnostics, University of Palermo, Via G. La Loggia n.1, Palermo, Sicily, Italy.
Sci Rep. 2021 Jan 13;11(1):867. doi: 10.1038/s41598-020-79110-7.
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.
评估认知功能障碍与左旋多巴诱导的运动障碍(LID)发展之间可能存在的关联。
从帕金森病认知障碍研究队列中招募了接受基线和随访神经心理学评估的 PD 患者。根据 MDS 二级标准诊断轻度认知障碍(PD-MCI)。评估了以下认知领域:情景记忆、注意力、执行功能、视空间功能和语言。当受试者在至少一项测试中得分低于每个领域的正态分布截断值 2 个标准差时,认为该领域存在障碍。在基线和随访时记录左旋多巴等效剂量、UPDRS-ME 和 LID。为了确定与随访时 LID 发展概率相关的可能神经心理学预测因素,使用 Cox 比例风险回归模型。
在纳入的 139 例 PD 患者中(87 名男性,平均年龄 65.7±9.4),18 例(12.9%)在基线时存在运动障碍。在基线时无运动障碍的 121 例患者中,22 例(18.1%)在随访时发生了 LID。注意力和执行域的损伤强烈预测了 LID 的发展(HR 4.45;95%CI 1.49-13.23 和 HR 3.46;95%CI 1.26-9.48)。注意力和执行域的损伤增加了发生运动障碍的风险,反映了共同皮质网络的改变。