• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

基于帕金森病新临床亚型的白质微观结构改变及相关神经生物学

Microstructural alterations in white matter and related neurobiology based on the new clinical subtypes of Parkinson's disease.

作者信息

Yuan Xiaorong, Yu Qiaowen, Liu Yanyan, Chen Jinge, Gao Jie, Liu Yujia, Song Ruxi, Zhang Yingzhi, Hou Zhongyu

机构信息

Department of Medical Imaging, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, Shandong, China.

Department of Medical Imaging, Shandong Provincial Hospital, Jinan, Shandong, China.

出版信息

Front Neurosci. 2024 Aug 1;18:1439443. doi: 10.3389/fnins.2024.1439443. eCollection 2024.

DOI:10.3389/fnins.2024.1439443
PMID:39148522
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11324559/
Abstract

BACKGROUND AND OBJECTIVES

The advent of new clinical subtyping systems for Parkinson's disease (PD) has led to the classification of patients into distinct groups: mild motor predominant (PD-MMP), intermediate (PD-IM), and diffuse malignant (PD-DM). Our goal was to evaluate the efficacy of diffusion tensor imaging (DTI) in the early diagnosis, assessment of clinical progression, and prediction of prognosis of these PD subtypes. Additionally, we attempted to understand the pathological mechanisms behind white matter damage using single-photon emission computed tomography (SPECT) and cerebrospinal fluid (CSF) analyses.

METHODS

We classified 135 de novo PD patients based on new clinical criteria and followed them up after 1 year, along with 45 healthy controls (HCs). We utilized tract-based spatial statistics to assess the microstructural changes of white matter at baseline and employed multiple linear regression to examine the associations between DTI metrics and clinical data at baseline and after follow-up.

RESULTS

Compared to HCs, patients with the PD-DM subtype demonstrated reduced fractional anisotropy (FA), increased axial diffusivity (AD), and elevated radial diffusivity (RD) at baseline. The FA and RD values correlated with the severity of motor symptoms, with RD also linked to cognitive performance. Changes in FA over time were found to be in sync with changes in motor scores and global composite outcome measures. Furthermore, baseline AD values and their rate of change were related to alterations in semantic verbal fluency. We also discovered the relationship between FA values and the levels of α-synuclein and β-amyloid. Reduced dopamine transporter uptake in the left putamen correlated with RD values in superficial white matter, motor symptoms, and autonomic dysfunction at baseline as well as cognitive impairments after 1 year.

CONCLUSIONS

The PD-DM subtype is characterized by severe clinical symptoms and a faster progression when compared to the other subtypes. DTI, a well-established technique, facilitates the early identification of white matter damage, elucidates the pathophysiological mechanisms of disease progression, and predicts cognitively related outcomes. The results of SPECT and CSF analyses can be used to explain the specific pattern of white matter damage in patients with the PD-DM subtype.

摘要

背景与目的

帕金森病(PD)新临床亚型分类系统的出现,使得患者被分为不同组别:轻度运动为主型(PD-MMP)、中间型(PD-IM)和弥漫恶性型(PD-DM)。我们的目标是评估弥散张量成像(DTI)在这些PD亚型的早期诊断、临床进展评估及预后预测中的效能。此外,我们试图通过单光子发射计算机断层扫描(SPECT)和脑脊液(CSF)分析来了解白质损伤背后的病理机制。

方法

我们根据新的临床标准对135例初发PD患者进行分类,并在1年后对其进行随访,同时纳入45名健康对照者(HCs)。我们利用基于纤维束的空间统计学方法评估基线时白质的微观结构变化,并采用多元线性回归分析来研究DTI指标与基线及随访后临床数据之间的关联。

结果

与HCs相比,PD-DM亚型患者在基线时表现出分数各向异性(FA)降低、轴向扩散率(AD)增加和径向扩散率(RD)升高。FA和RD值与运动症状严重程度相关,RD还与认知表现有关。发现FA随时间的变化与运动评分和整体综合结局指标的变化同步。此外,基线AD值及其变化率与语义言语流畅性的改变有关。我们还发现了FA值与α-突触核蛋白和β-淀粉样蛋白水平之间的关系。左侧壳核多巴胺转运体摄取减少与基线时浅表白质的RD值、运动症状和自主神经功能障碍以及1年后的认知障碍相关。

结论

与其他亚型相比,PD-DM亚型具有严重的临床症状和更快的进展速度。DTI作为一种成熟的技术,有助于早期识别白质损伤,阐明疾病进展的病理生理机制,并预测与认知相关的结局。SPECT和CSF分析结果可用于解释PD-DM亚型患者白质损伤的特定模式。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1831/11324559/43ecd0bbf48e/fnins-18-1439443-g0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1831/11324559/9a91fec1a02d/fnins-18-1439443-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1831/11324559/63166d336a17/fnins-18-1439443-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1831/11324559/251c27b9a3f1/fnins-18-1439443-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1831/11324559/abe8fdcef29e/fnins-18-1439443-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1831/11324559/4833dbd193ac/fnins-18-1439443-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1831/11324559/2ea75d8dc2c3/fnins-18-1439443-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1831/11324559/43ecd0bbf48e/fnins-18-1439443-g0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1831/11324559/9a91fec1a02d/fnins-18-1439443-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1831/11324559/63166d336a17/fnins-18-1439443-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1831/11324559/251c27b9a3f1/fnins-18-1439443-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1831/11324559/abe8fdcef29e/fnins-18-1439443-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1831/11324559/4833dbd193ac/fnins-18-1439443-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1831/11324559/2ea75d8dc2c3/fnins-18-1439443-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1831/11324559/43ecd0bbf48e/fnins-18-1439443-g0007.jpg

相似文献

1
Microstructural alterations in white matter and related neurobiology based on the new clinical subtypes of Parkinson's disease.基于帕金森病新临床亚型的白质微观结构改变及相关神经生物学
Front Neurosci. 2024 Aug 1;18:1439443. doi: 10.3389/fnins.2024.1439443. eCollection 2024.
2
Progressive Decline in Gray and White Matter Integrity in Parkinson's Disease: An Analysis of Longitudinal Parkinson Progression Markers Initiative Diffusion Tensor Imaging Data.帕金森病中灰质和白质完整性的渐进性下降:帕金森病纵向进展标志物计划扩散张量成像数据分析
Front Aging Neurosci. 2018 Oct 8;10:318. doi: 10.3389/fnagi.2018.00318. eCollection 2018.
3
Progression of Regional Microstructural Degeneration in Parkinson's Disease: A Multicenter Diffusion Tensor Imaging Study.帕金森病区域微观结构退变的进展:一项多中心扩散张量成像研究
PLoS One. 2016 Oct 31;11(10):e0165540. doi: 10.1371/journal.pone.0165540. eCollection 2016.
4
Differential White Matter Regional Alterations in Motor Subtypes of Early Drug-Naive Parkinson's Disease Patients.早期未经药物治疗的帕金森病运动亚型患者的白质区域差异改变。
Neurorehabil Neural Repair. 2018 Feb;32(2):129-141. doi: 10.1177/1545968317753075. Epub 2018 Jan 19.
5
Relationship Between DTI Metrics and Cognitive Function in Alzheimer's Disease.阿尔茨海默病中扩散张量成像指标与认知功能的关系
Front Aging Neurosci. 2019 Jan 9;10:436. doi: 10.3389/fnagi.2018.00436. eCollection 2018.
6
Diffusion basis spectrum imaging detects pathological alterations in substantia nigra and white matter tracts with early-stage Parkinson's disease.扩散张量谱成像检测早期帕金森病患者黑质和白质束的病理改变。
Eur Radiol. 2023 Dec;33(12):9109-9119. doi: 10.1007/s00330-023-09780-0. Epub 2023 Jul 12.
7
Diffusion tensor metrics, motor and non-motor symptoms in de novo Parkinson's disease.弥散张量指标与新发帕金森病的运动及非运动症状
Neuroradiology. 2024 Nov;66(11):1955-1966. doi: 10.1007/s00234-024-03452-6. Epub 2024 Aug 27.
8
Diffusion tensor imaging techniques show that parkin gene S/N167 polymorphism is responsible for extensive brain white matter damage in patients with Parkinson's disease.扩散张量成像技术显示,帕金森病患者中帕金基因S/N167多态性是广泛脑白质损伤的原因。
Heliyon. 2023 Jul 31;9(8):e18395. doi: 10.1016/j.heliyon.2023.e18395. eCollection 2023 Aug.
9
Multifocal alterations of white matter accompany the transition from normal cognition to dementia in Parkinson's disease patients.帕金森病患者从正常认知向痴呆转变时伴有脑白质多灶性改变。
Brain Imaging Behav. 2019 Feb;13(1):232-240. doi: 10.1007/s11682-018-9863-7.
10
Executive function network's white matter alterations relate to Parkinson's disease motor phenotype.执行功能网络的白质改变与帕金森病的运动表型有关。
Neurosci Lett. 2021 Jan 10;741:135486. doi: 10.1016/j.neulet.2020.135486. Epub 2020 Nov 5.

本文引用的文献

1
White matter changes in Parkinson's disease.帕金森病中的白质变化。
NPJ Parkinsons Dis. 2023 Oct 31;9(1):150. doi: 10.1038/s41531-023-00592-z.
2
Alpha-synuclein fibrils amplified from multiple system atrophy and Parkinson's disease patient brain spread after intracerebral injection into mouse brain.从多位多系统萎缩症和帕金森病患者大脑中扩增的α-突触核蛋白纤维在脑内注射到小鼠大脑后会扩散。
Brain Pathol. 2023 Sep;33(5):e13196. doi: 10.1111/bpa.13196. Epub 2023 Jul 24.
3
Association of Cortical Gyrification With Imaging and Serum Biomarkers in Patients With Parkinson Disease.
帕金森病患者皮质脑回与影像学和血清生物标志物的相关性。
Neurology. 2023 Jul 18;101(3):e311-e323. doi: 10.1212/WNL.0000000000207410. Epub 2023 Jun 2.
4
Cognitive heterogeneity in Parkinson's disease: A mechanistic view.帕金森病认知异质性:一种机制观点。
Neuron. 2023 May 17;111(10):1531-1546. doi: 10.1016/j.neuron.2023.03.021. Epub 2023 Apr 6.
5
White and gray matter alterations in de novo PD patients: which matter most?首发 PD 患者的脑白质和灰质改变:哪些最重要?
J Neurol. 2023 May;270(5):2734-2742. doi: 10.1007/s00415-023-11607-3. Epub 2023 Feb 11.
6
Aberrant corticospinal tract characteristics in prodromal PD: A diffusion tensor imaging study.前驱期帕金森病中皮质脊髓束的异常特征:一项扩散张量成像研究。
Clin Park Relat Disord. 2022 Dec 19;8:100182. doi: 10.1016/j.prdoa.2022.100182. eCollection 2023.
7
α-Synuclein in synaptic function and dysfunction.α-突触核蛋白在突触功能及功能障碍中的作用。
Trends Neurosci. 2023 Feb;46(2):153-166. doi: 10.1016/j.tins.2022.11.007. Epub 2022 Dec 23.
8
Identification and prediction of Parkinson's disease subtypes and progression using machine learning in two cohorts.在两个队列中使用机器学习识别和预测帕金森病的亚型及进展
NPJ Parkinsons Dis. 2022 Dec 16;8(1):172. doi: 10.1038/s41531-022-00439-z.
9
Association Between White Matter Networks and the Pattern of Striatal Dopamine Depletion in Patients With Parkinson Disease.帕金森病患者白质网络与纹状体多巴胺耗竭模式的关系。
Neurology. 2022 Dec 12;99(24):e2672-e2682. doi: 10.1212/WNL.0000000000201269.
10
Genetics and Pathogenesis of Parkinson's Syndrome.帕金森综合征的遗传学与发病机制。
Annu Rev Pathol. 2023 Jan 24;18:95-121. doi: 10.1146/annurev-pathmechdis-031521-034145. Epub 2022 Sep 13.