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快速眼动睡眠行为障碍与帕金森病患者纹状体多巴胺缺失。

Rapid eye movement sleep behaviour disorder and striatal dopamine depletion in patients with Parkinson's disease.

机构信息

Department of Neurology, Yonsei University College of Medicine, Seoul, South Korea.

Department of Neurology, Myongji Hospital, Goyang, South Korea.

出版信息

Eur J Neurol. 2017 Oct;24(10):1314-1319. doi: 10.1111/ene.13388. Epub 2017 Aug 7.

Abstract

BACKGROUND AND PURPOSE

Rapid eye movement sleep behaviour disorder (RBD) is related to striatal dopamine depletion. This study was performed to confirm whether clinically probable RBD (cpRBD) in patients with Parkinson's disease (PD) is associated with a specific pattern of striatal dopamine depletion.

METHODS

A prospective survey was conducted using the RBD Screening Questionnaire (RBDSQ) in 122 patients with PD who had undergone dopamine transporter (DAT) positron emission tomography scan.

RESULTS

Patients with cpRBD (RBDSQ ≥ 7) exhibited greater motor deficits, predominantly in the less-affected side and axial symptoms, and were prescribed higher levodopa-equivalent doses at follow-up than those without cpRBD (RBDSQ ≤ 4), despite their similar disease and treatment durations. Compared to patients without cpRBD, those with cpRBD showed lower DAT activities in the putamen, particularly in the less-affected side in all putaminal subregions, and a tendency to be lower in the ventral striatum. In addition, greater motor deficits in patients with cpRBD than in those without cpRBD remained significant after controlling for DAT binding in the putamen and other confounding variables.

CONCLUSIONS

These results demonstrated that the presence of RBD in patients with PD is associated with different patterns of both motor deficit distribution and striatal DAT depletion, suggesting that the presence of RBD represents a distinct PD subtype with a malignant motor parkinsonism.

摘要

背景与目的

快速眼动睡眠行为障碍(RBD)与纹状体多巴胺耗竭有关。本研究旨在确认帕金森病(PD)患者的临床可能 RBD(cpRBD)是否与纹状体多巴胺耗竭的特定模式相关。

方法

使用 RBD 筛查问卷(RBDSQ)对 122 例接受多巴胺转运蛋白(DAT)正电子发射断层扫描的 PD 患者进行前瞻性调查。

结果

RBDSQ≥7 的 cpRBD 患者表现出更大的运动缺陷,主要在受影响较小的一侧和轴症状,并且在随访时开的左旋多巴等效剂量更高,尽管他们的疾病和治疗持续时间相似。与无 cpRBD 患者相比,cpRBD 患者的壳核 DAT 活性较低,尤其是所有壳核亚区的受影响较小的一侧,且腹侧纹状体的活性也有降低的趋势。此外,在控制壳核 DAT 结合和其他混杂变量后,cpRBD 患者的运动缺陷较无 cpRBD 患者更为显著。

结论

这些结果表明,PD 患者存在 RBD 与运动缺陷分布和纹状体 DAT 耗竭的不同模式有关,表明 RBD 的存在代表了一种具有恶性帕金森运动障碍的独特 PD 亚型。

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