Cao Ruihua, Ma Ruolin, Wang Kai, Hu Panpan
Department of Neurology, The First Affiliated Hospital of Anhui Medical University, Hefei, China.
Hefei Comprehensive National Science Center, Institute of Artificial Intelligence, Hefei, China.
Front Neurol. 2022 Jun 10;13:880583. doi: 10.3389/fneur.2022.880583. eCollection 2022.
REM sleep behavior disorder (RBD) is closely associated with Parkinson's disease (PD), however, the influence of dopaminergic replacement therapy (DRT) on the clinical course of RBD in PD remains less understood. The objective of our study is to investigate how DRTs modify the evolution of RBD in a longitudinal cohort study of initially PD patients. Four hundred and five drug-naive patients with early-stage PD were included. RBD symptoms were assessed using the 10-item RBD Screening Questionnaire (RBDSQ) at baseline and during the 5-year follow-up. A generalized estimating equation was used to examine predictors of the evolution of RBD symptoms. For patients without baseline pRBD, patients on levodopa treatment showed a greater increase in RBDSQ scores than those not on levodopa treatment, and the increase in RBDSQ scores was significantly correlated with the levodopa-LEDD. Moreover, the changes in RBDSQ scores at a given post-baseline visit were significantly associated with the use of levodopa (OR = 1.875, = 0.008) and the combined use of levodopa and DA (OR = 2.188, = 0.012), as well as the levodopa-LEDD (OR = 1.001, = 0.005) at that visit. The use of DA alone or the DA-LEDD was not a significant predictor of changes in RBDSQ scores. Similarly, a conversion from pRBD negative to pRBD positive was significantly associated with levodopa-LEDD (OR = 1.001, = 0.014) but not DA-LEDD. Together, these finding implicated that the use of levodopa may act as a contributing factor to the increasing prevalence of RBD after the onset of PD, suggesting different mechanisms underlying prodromal RBD and late-onset RBD.
快速眼动睡眠行为障碍(RBD)与帕金森病(PD)密切相关,然而,多巴胺能替代疗法(DRT)对PD患者RBD临床病程的影响仍了解较少。我们研究的目的是在一项对初诊PD患者的纵向队列研究中,调查DRT如何改变RBD的演变。纳入了405例未经药物治疗的早期PD患者。在基线和5年随访期间,使用10项RBD筛查问卷(RBDSQ)评估RBD症状。采用广义估计方程来检查RBD症状演变的预测因素。对于无基线期前驱RBD的患者,接受左旋多巴治疗的患者RBDSQ评分的增加幅度大于未接受左旋多巴治疗的患者,且RBDSQ评分的增加与左旋多巴等效剂量(LEDD)显著相关。此外,在给定的基线后访视时,RBDSQ评分的变化与左旋多巴的使用(比值比[OR]=1.875,P=0.008)、左旋多巴与多巴胺能药物的联合使用(OR=2.188,P=0.012)以及该访视时的左旋多巴LEDD(OR=1.001,P=0.005)显著相关。单独使用多巴胺能药物或多巴胺能药物LEDD不是RBDSQ评分变化的显著预测因素。同样,从前驱RBD阴性转变为前驱RBD阳性与左旋多巴LEDD显著相关(OR=1.001,P=0.014),但与多巴胺能药物LEDD无关。总之,这些发现表明左旋多巴的使用可能是PD发病后RBD患病率增加的一个促成因素,提示前驱RBD和晚发型RBD存在不同的潜在机制。