Medical School, Federal University of Santa Maria (UFSM), Santa Maria, Brazil.
Department of Biochemistry, Federal University of Santa Maria (UFSM), Santa Maria, Brazil.
Mov Disord Clin Pract. 2024 Oct;11(10):1195-1202. doi: 10.1002/mdc3.14198. Epub 2024 Aug 27.
There has been a long debate whether delaying treatment with levodopa prevents motor complications in Parkinson's disease (PD).
We performed a meta-analysis on randomized clinical trials (RCTs) that compared early- versus delayed-start treatment with levodopa in PD.
A systematic review was conducted in PubMed, EMBASE, and Web of Science databases from inception to July 1, 2023. Only RCTs that compared early and delayed levodopa treatment in PD were included. Non-randomized comparisons from follow-up studies were included as well. Our primary outcomes were occurrence of overall motor complications, motor fluctuations, and dyskinesias.
Seven studies with a total of 1149 patients (636 in the early-start group and 513 in the delayed-start) were included in our analysis. There was no difference between groups regarding motor complications (OR 1.39; 95% CI: 0.68-1.72; P = 0.37) or dyskinesias (OR 1.52; 95% CI: 0.90-2.57; P = 0.11). Motor fluctuations occurred less frequently in the early-start group (OR 0.70; 95% CI: 0.52-0.95; P = 0.02). Nonetheless, on subgroup analysis of dopamine agonists, rate of dyskinesias was smaller in the delayed-start group (OR 1.82; 95% CI: 1.08-3.07; P = 0.03).
Delaying treatment with levodopa does not seem to prevent levodopa-related motor complications in PD. Adjunct treatment with dopamine agonists may reduce the need for higher doses of levodopa and thus reduce the risk for dyskinesias but this practice is often associated with a higher frequency of adverse effects related to dopamine agonists.
关于延迟左旋多巴治疗是否可以预防帕金森病(PD)的运动并发症,一直存在着长期的争论。
我们对比较 PD 中左旋多巴早期与延迟开始治疗的随机临床试验(RCT)进行了荟萃分析。
从 2023 年 7 月 1 日起,我们在 PubMed、EMBASE 和 Web of Science 数据库中进行了系统综述。仅纳入比较 PD 中早期和延迟左旋多巴治疗的 RCT。也纳入了随访研究中的非随机比较。我们的主要结局是观察总的运动并发症、运动波动和运动障碍的发生情况。
共有 7 项研究,共纳入 1149 名患者(早期起始组 636 名,延迟起始组 513 名)纳入我们的分析。两组间在运动并发症(OR 1.39;95%CI:0.68-1.72;P=0.37)或运动障碍(OR 1.52;95%CI:0.90-2.57;P=0.11)方面无差异。早期起始组运动波动的发生率较低(OR 0.70;95%CI:0.52-0.95;P=0.02)。然而,在多巴胺激动剂的亚组分析中,延迟起始组的运动障碍发生率较小(OR 1.82;95%CI:1.08-3.07;P=0.03)。
延迟左旋多巴治疗似乎并不能预防 PD 中的左旋多巴相关运动并发症。多巴胺激动剂的辅助治疗可能会减少对更高剂量左旋多巴的需求,从而降低运动障碍的风险,但这种做法通常与与多巴胺激动剂相关的不良反应发生率更高有关。