Longitudinal decline in DAT binding in Parkinson's disease: connections with sleep disturbances.

IF 7 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL
Junli Ren, Haobo Xie, Yiyun Weng, Yaoying Ge, Ruotong Yao, Zihan Jiang, Jinxiu Zhang, Yusheng Zhu, Xiaotong Fu, Junchao Wang, Zijia Liu, Shishu Zhang, Tingxuan Zhang, Guangyong Chen, Dehao Yang
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引用次数: 0

Abstract

Background: The nigrostriatal dopamine (DA) system plays a critical role in regulating the sleep-wake state. The relationship between baseline striatal DA transporter (DAT) specific binding ratios (SBR) and rapid eye movement sleep behavior disorder (RBD) has been established. This study aimed to investigate the association between the progression of striatal DA dysfunction and sleep disturbances, including excessive daytime sleepiness (EDS) and probable RBD (pRBD), in patients with Parkinson's disease (PD).

Methods: Data were obtained from the Parkinson's Progression Markers Initiative (PPMI). Six hundred twenty-one newly diagnosed PD patients and followed up for 4 years were included in this longitudinal study. EDS and pRBD were defined using the Epworth Sleepiness Scale (ESS) and RBD Screening Questionnaire (RBDSQ). Striatal DAT SBR was evaluated by [123I] FP-CIT SPECT.

Results: Using a linear mixed-effects model across all contemporaneous data points, we found a negative correlation between striatal DAT SBR and sleep disturbances (EDS/pRBD). The interaction between striatal DAT SBR and year was specific to RBDSQ score (β = - 0.102, 95% CI: - 0.187 to - 0.017, p = 0.019), with no evidence of a similar interaction for ESS score. Additionally, the association between the alpha-synuclein gene (SNCA) and sleep disturbances was mediated by the SBR (ESS score: total effect = - 2.717, p = 0.022; direct effect = - 3.222, p = 0.007; indirect effect = 0.505, p < 0.05; RBDSQ score: total effect = 1.402, p = 0.026; direct effect = 1.209, p = 0.057; indirect effect = 0.193, p < 0.05).

Conclusions: Our findings support the role of striatal DA dysfunction in sleep disturbances in early PD patients. Furthermore, we demonstrated that genetic variations in causative genes of PD contribute to the development of sleep disturbances. Striatal DAT imaging may be a useful risk indicator for sleep disturbances, providing early intervention strategies.

帕金森病患者 DAT 结合力的纵向下降:与睡眠障碍的关系。
背景:黑质纹状体多巴胺(DA)系统在调节睡眠-觉醒状态中起着至关重要的作用。纹状体DA转运体(DAT)特异性结合率(SBR)基线与快速眼动睡眠行为障碍(RBD)之间的关系已经确定。本研究旨在调查帕金森病(PD)患者纹状体 DA 功能障碍的进展与睡眠障碍(包括白天过度嗜睡(EDS)和可能的 RBD(pRBD))之间的关系:数据来自帕金森病进展标志物倡议(PPMI)。这项纵向研究纳入了 621 名新诊断的帕金森病患者,并对他们进行了为期 4 年的随访。采用埃普沃思嗜睡量表(ESS)和RBD筛查问卷(RBDSQ)对EDS和pRBD进行了定义。纹状体 DAT SBR 通过 [123I] FP-CIT SPECT 进行评估:通过对所有同期数据点进行线性混合效应模型分析,我们发现纹状体 DAT SBR 与睡眠障碍(EDS/pRBD)之间存在负相关。纹状体 DAT SBR 与年份之间的交互作用与 RBDSQ 评分有关(β = - 0.102,95% CI:- 0.187 到 - 0.017,p = 0.019),ESS 评分没有类似的交互作用。此外,α-突触核蛋白基因(SNCA)与睡眠障碍之间的关联是由 SBR 介导的(ESS 评分:总效应 = - 2.717,p = 0.022;直接效应 = - 3.222,p = 0.007;间接效应 = 0.505,p 结论:我们的研究结果支持纹状体在睡眠障碍中的作用:我们的研究结果支持纹状体 DA 功能障碍在早期帕金森病患者睡眠障碍中的作用。此外,我们还证明了帕金森病致病基因的遗传变异会导致睡眠障碍的发生。纹状体DAT成像可能是睡眠障碍的有用风险指标,可提供早期干预策略。
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来源期刊
BMC Medicine
BMC Medicine 医学-医学:内科
CiteScore
13.10
自引率
1.10%
发文量
435
审稿时长
4-8 weeks
期刊介绍: BMC Medicine is an open access, transparent peer-reviewed general medical journal. It is the flagship journal of the BMC series and publishes outstanding and influential research in various areas including clinical practice, translational medicine, medical and health advances, public health, global health, policy, and general topics of interest to the biomedical and sociomedical professional communities. In addition to research articles, the journal also publishes stimulating debates, reviews, unique forum articles, and concise tutorials. All articles published in BMC Medicine are included in various databases such as Biological Abstracts, BIOSIS, CAS, Citebase, Current contents, DOAJ, Embase, MEDLINE, PubMed, Science Citation Index Expanded, OAIster, SCImago, Scopus, SOCOLAR, and Zetoc.
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