Ye Guanyu, Xu Xiaomeng, Zhou Liche, Zhao Aonan, Zhu Lin, Liu Jun
Department of Neurology and Institute of Neurology, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
CAS Center for Excellence in Brain Science and Intelligence Technology, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
NPJ Parkinsons Dis. 2022 Apr 5;8(1):36. doi: 10.1038/s41531-022-00303-0.
The course of REM sleep behavior disorder (RBD) variates in the early stage of Parkinson's disease. We aimed to delineate the association between the evolution pattern of probable RBD (pRBD) and the progression of Parkinson's disease (PD). 281 de novo PD patients from the Parkinson's Progression Markers Initiative database were included. Patients were followed up for a mean of 6.8 years and were classified into different groups according to the evolution patterns of pRBD. Disease progression was compared among groups using survival analysis, where the endpoint was defined as progression to Hoehn-Yahr stage 3 or higher for motor progression and progression to mild cognitive impairment for cognitive decline. At the 4th year of follow-up, four types of pRBD evolution patterns were identified: (1) non-RBD-stable (55.5%): patients persistently free of pRBD; (2) late-RBD (12.1%): patients developed pRBD during follow-up; (3) RBD-stable (24.9%): patients showed persistent pRBD, and (4) RBD-reversion (7.5%): patients showed pRBD at baseline which disappeared during follow-up. The RBD-reversion type showed the fastest motor progression while the RBD-stable type showed the fastest cognitive decline. At baseline, the RBD-reversion type showed the most severe gray matter atrophy in the middle frontal gyrus, while the RBD-stable type showed gray matter atrophy mainly in the para-hippocampal gyrus. Four types of early pRBD evolution patterns featured different brain lesions and predicted different courses of motor and cognitive decline in PD.
快速眼动睡眠行为障碍(RBD)在帕金森病早期的病程有所不同。我们旨在阐明疑似RBD(pRBD)的演变模式与帕金森病(PD)进展之间的关联。纳入了帕金森病进展标志物倡议数据库中的281例新发PD患者。患者平均随访6.8年,并根据pRBD的演变模式分为不同组。使用生存分析比较各组间的疾病进展,其中终点定义为运动进展至Hoehn-Yahr 3期或更高,以及认知下降至轻度认知障碍。在随访第4年时,确定了四种pRBD演变模式:(1)非RBD稳定型(55.5%):患者持续无pRBD;(2)迟发型RBD(12.1%):患者在随访期间出现pRBD;(3)RBD稳定型(24.9%):患者持续存在pRBD,以及(4)RBD逆转型(7.5%):患者在基线时出现pRBD,但在随访期间消失。RBD逆转型显示运动进展最快,而RBD稳定型显示认知下降最快。在基线时,RBD逆转型在额中回显示最严重的灰质萎缩,而RBD稳定型主要在海马旁回显示灰质萎缩。四种早期pRBD演变模式具有不同的脑损伤,并预测了PD中运动和认知下降的不同病程。