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纹状体血脑屏障在帕金森病痴呆中的开放:一项探索性的初步研究。

Striatal Blood-Brain Barrier Opening in Parkinson's Disease Dementia: A Pilot Exploratory Study.

机构信息

HM CINAC (Centro Integral de Neurociencias Abarca Campal), Fundación Hospitales de Madrid, Hospital Universitario HM Puerta del Sur, HM Hospitales, Madrid, Spain.

Network Center for Biomedical Research on Neurodegenerative Diseases (CIBERNED), Instituto Carlos III, Madrid, Spain.

出版信息

Mov Disord. 2022 Oct;37(10):2057-2065. doi: 10.1002/mds.29134. Epub 2022 Jun 28.


DOI:10.1002/mds.29134
PMID:35765711
Abstract

BACKGROUND: Parkinson's disease (PD) exhibits a high prevalence of dementia as disease severity and duration progress. Focused ultrasound (FUS) has been applied for transient blood-brain barrier (BBB) opening of cortical regions in neurodegenerative disorders. The striatum is a primary target for delivery of putative therapeutic agents in PD. OBJECTIVE: Here, we report a prospective, single-arm, nonrandomized, proof-of-concept, phase I clinical trial (NCT03608553 amended) in PD with dementia to test the safety and feasibility of striatal BBB opening in PD patients. METHODS: Seven PD patients with cognitive impairment were treated for BBB opening in the posterior putamen. This was performed in two sessions separated by 2 to 4 weeks, where the second session included bilateral putamina opening in 3 patients. Primary outcome measures included safety and feasibility of focal striatal BBB opening. Changes in motor and cognitive functions, magnetic resonance imaging (MRI), F-fluorodopa (FDOPA), and β-amyloid PET (positron emission tomography) images were determined. RESULTS: The procedure was feasible and well tolerated, with no serious adverse events. No neurologically relevant change in motor and cognitive (battery of neuropsychological tests) functions was recognized at follow-up. MRI revealed putamen BBB closing shortly after treatment (24 hours to 14 days) and ruled out hemorrhagic and ischemic lesions. There was a discrete but significant reduction in β-amyloid uptake in the targeted region and no change in FDOPA PET. CONCLUSIONS: These initial results indicate that FUS-mediated striatal BBB opening is feasible and safe and therefore could become an effective tool to facilitate the delivery of putative neurorestorative molecules in PD. © 2022 International Parkinson and Movement Disorder Society.

摘要

背景:帕金森病(PD)随着疾病严重程度和病程的进展,表现出较高的痴呆患病率。聚焦超声(FUS)已应用于神经退行性疾病皮质区域的短暂性血脑屏障(BBB)开放。纹状体是 PD 中潜在治疗药物传递的主要靶标。

目的:本研究报道了一项前瞻性、单臂、非随机、概念验证、I 期临床试验(NCT03608553 修正案),旨在评估 FUS 介导的 PD 患者纹状体 BBB 开放的安全性和可行性。

方法:7 名认知障碍 PD 患者接受了后纹状体 BBB 开放治疗。该治疗在 2 至 4 周的间隔内进行两次,其中 3 名患者在第二次治疗中进行双侧纹状体开放。主要终点包括聚焦式纹状体 BBB 开放的安全性和可行性。评估运动和认知功能、磁共振成像(MRI)、氟多巴(FDOPA)和β-淀粉样蛋白正电子发射断层扫描(PET)的变化。

结果:该过程是可行的,并且患者耐受性良好,无严重不良事件。在随访时,未发现运动和认知功能(神经心理学测试组合)的神经相关变化。MRI 显示治疗后纹状体 BBB 迅速关闭(24 小时至 14 天),并排除了出血和缺血性病变。目标区域的β-淀粉样蛋白摄取有明显但离散的减少,FDOPA PET 无变化。

结论:这些初步结果表明,FUS 介导的纹状体 BBB 开放是可行且安全的,因此可能成为促进 PD 中潜在神经修复分子传递的有效工具。 © 2022 国际帕金森病和运动障碍学会。

相似文献

[1]
Striatal Blood-Brain Barrier Opening in Parkinson's Disease Dementia: A Pilot Exploratory Study.

Mov Disord. 2022-10

[2]
Blood-brain barrier opening with focused ultrasound in Parkinson's disease dementia.

Nat Commun. 2021-2-3

[3]
Focused ultrasound-mediated blood-brain barrier opening in Alzheimer's disease: long-term safety, imaging, and cognitive outcomes.

J Neurosurg. 2023-7-1

[4]
Nigrostriatal blood-brain barrier opening in Parkinson's disease.

J Neurol Neurosurg Psychiatry. 2024-10-16

[5]
Rate of 6-[18F]fluorodopa uptake decline in striatal subregions in Parkinson's disease.

Mov Disord. 2011-3-29

[6]
Extensive frontal focused ultrasound mediated blood-brain barrier opening for the treatment of Alzheimer's disease: a proof-of-concept study.

Transl Neurodegener. 2021-11-5

[7]
Complementary positron emission tomographic studies of the striatal dopaminergic system in Parkinson's disease.

Arch Neurol. 1995-12

[8]
Slowing of EEG waves correlates with striatal [ F]fluorodopa PET/CT uptake and executive dysfunction in Parkinson's disease.

Eur J Neurosci. 2023-11

[9]
Contralateral Posterior Putaminal F-Fluorodopa Uptake in Mild Stage Parkinson's Disease: A PET/CT Study.

Curr Neurovasc Res. 2021

[10]
Regional striatal DOPA transport and decarboxylase activity in Parkinson's disease.

J Nucl Med. 1995-7

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ACS Omega. 2025-7-22

[2]
Blood‑brain barrier dysfunction in epilepsy: Mechanisms, therapeutic strategies and future orientation (Review).

Int J Mol Med. 2025-9

[3]
Acoustic hologram-enabled simultaneous multi-target blood-brain barrier opening (AH-SiMBO).

Commun Eng. 2025-6-2

[4]
Drug delivery strategies to cross the blood-brain barrier in Alzheimer's disease: a comprehensive review on three promising strategies.

J Prev Alzheimers Dis. 2025-8

[5]
The blood-brain barriers: novel nanocarriers for central nervous system diseases.

J Nanobiotechnology. 2025-2-26

[6]
Holographic Ultrasound Modulates Neural Activity in a 1-Methyl-4-Phenyl-1,2,3,6-Tetrahydropyridine-Induced Mouse Model of Parkinson's Disease.

Research (Wash D C). 2024-11-6

[7]
Clinical Applications of Micro/Nanobubble Technology in Neurological Diseases.

Biomimetics (Basel). 2024-10-20

[8]
A review of temporal interference, nanoparticles, ultrasound, gene therapy, and designer receptors for Parkinson disease.

NPJ Parkinsons Dis. 2024-10-23

[9]
Brain Nucleic Acid Delivery and Genome Editing via Focused Ultrasound-Mediated Blood-Brain Barrier Opening and Long-Circulating Nanoparticles.

ACS Nano. 2024-9-3

[10]
An Overview on the Physiopathology of the Blood-Brain Barrier and the Lipid-Based Nanocarriers for Central Nervous System Delivery.

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