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Risk factors for levodopa-induced dyskinesia in Parkinson’s disease patients

机译:帕金森病患者左旋多巴诱发运动障碍的危险因素

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Background/Aim. Levodopa, the precursor of dopamine, is a substitute therapy for Parkinson''s disease. Long-term application of levodopa causes fluctuation in motor response and the occurrence of involuntary movements or dyskinesia. The aim of this study was to assess the risk factors for dyskinesia in Parkinson’s disease (PD) patients undergoing treatment with levodopa. Methods. We included 177 consecutive outpatients with PD, who had been undergoing treatment for at least six months. A semi-structured interview was used to collect demo-graphic and clinical data as well as a number of clinical scales. Results. Patients with dyskinesia (n = 90) were younger at dis-ease onset and had longer disease duration. They had higher Unified Parkinson''s Disease Rating Scale (UPDRS) scores and more frequently had other motor complications, such as wearing-off and freezing of gait, as well as non-motor ones, such as psychosis. They took higher levodopa doses and levodopa equivalent doses and were on levodopa therapy for a longer period of time. Multivariate analysis yielded that in-dependent risk factors for dyskinesia were: disease duration of longer than 10 years [relative risk (RR = 2.90), 95% confidence interval (CI) 1.19–7.10; p = 0.019), dopaminergic treatment duration of longer than 94 months (RR = 3.21, 95% confidence interval (CI) 1.05–9.87; p = 0.041) and levodopa dosage of higher than 537 mg (RR = 3.62, 95%IP 1.57–8.35; p = 0.002). Conclusion. We highlight the importance of known risk factors for dyskinesia and their occurrence in the context of advanced, complicated disease. [Project of the Serbian Ministry of Education, Science and Technological Development, Grant no. 175090]
机译:背景/目标。多巴胺的前体左旋多巴是帕金森氏病的替代疗法。长期使用左旋多巴会引起运动反应波动以及不自主运动或运动障碍的发生。这项研究的目的是评估接受左旋多巴治疗的帕金森氏病(PD)患者运动障碍的危险因素。方法。我们纳入了连续接受治疗至少六个月的177例PD门诊患者。使用半结构化访谈收集人口统计和临床数据以及许多临床量表。结果。运动障碍患者(n = 90)在疾病发作时年龄较小,病程较长。他们的帕金森综合症疾病评分量表(UPDRS)得分较高,其他运动并发症(如脚步磨损和冻结)以及非运动障碍(如精神病)的发生频率更高。他们服用了更高的左旋多巴剂量和左旋多巴等效剂量,并且接受了左旋多巴治疗更长的时间。多变量分析表明,运动障碍的独立危险因素为:疾病持续时间超过10年[相对风险(RR = 2.90),95%置信区间(CI)1.19–7.10; p = 0.019),多巴胺能治疗持续时间超过94个月(RR = 3.21,95%置信区间(CI)1.05-9.87; p = 0.041),左旋多巴的剂量高于537 mg(RR = 3.62,95%IP 1.57) –8.35; p = 0.002)。结论。我们强调了运动障碍的已知危险因素及其在晚期复杂疾病中的发生的重要性。 [塞尔维亚教育,科学和技术发展部的项目,赠款175090]

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