新帕金森病的弥散张量指标、运动和非运动症状。

IF 2.4 3区 医学 Q2 CLINICAL NEUROLOGY Neuroradiology Pub Date : 2024-08-27 DOI:10.1007/s00234-024-03452-6
Nayron Medeiros Soares, Pedro Henrique Rodrigues da Silva, Gabriela Magalhães Pereira, Renata Ferranti Leoni, Carlos Roberto de Mello Rieder, Thatiane Alves Pianoschi Alva
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引用次数: 0

摘要

简介帕金森病(PD)是一种以黑质多巴胺能神经元变性为特征的神经退行性疾病,表现为运动和非运动症状。我们假设扩散指标的改变与新发帕金森病患者的临床症状有关:方法:我们对 55 名新发型帕金森病患者(58.62 ± 9.85 岁,37 名男性)和 55 名年龄匹配的健康对照者(59.92 ± 11.25 岁,34 名男性)的分数各向异性(FA)、平均值(MD)、轴向(AD)和径向扩散率(RD)进行了评估。弥散加权图像和临床变量来自帕金森病进展标志物倡议研究。使用基于纤维束的空间统计来识别白质(WM)变化,并使用JHU-WM纤维束成像图谱对纤维束进行定位。对患者的运动和非运动症状进行了评估:我们观察到,与对照组相比,患者各种纤维束的 FA 值更高,RD 值更低(p-TFCE 结论):我们的研究结果表明,新发帕金森病纤维束的微结构发生了变化;然而,与临床症状的关联有限,这揭示了帕金森病病理的复杂性。这些研究结果可能有助于了解帕金森病的神经生物学变化,并对制定有针对性的干预措施有一定的意义。然而,要阐明新发型帕金森病这些弥散改变的潜在机制,还需要对更大的队列进行进一步的纵向研究,并考虑混杂因素。
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Diffusion tensor metrics, motor and non-motor symptoms in de novo Parkinson's disease.

Introduction: Parkinson's disease (PD) is a neurodegenerative disorder characterized by dopaminergic neurons' degeneration of the substantia nigra, presenting with motor and non-motor symptoms. We hypothesized that altered diffusion metrics are associated with clinical symptoms in de novo PD patients.

Methods: Fractional Anisotropy (FA) and Mean (MD), Axial (AD), and Radial Diffusivity (RD) were assessed in 55 de novo PD patients (58.62 ± 9.85 years, 37 men) and 55 age-matched healthy controls (59.92 ± 11.25 years, 34 men). Diffusion-weighted images and clinical variables were collected from the Parkinson's Progression Markers Initiative study. Tract-based spatial statistics were used to identify white matter (WM) changes, and fiber tracts were localized using the JHU-WM tractography atlas. Motor and non-motor symptoms were evaluated in patients.

Results: We observed higher FA values and lower RD values in patients than controls in various fiber tracts (p-TFCE < 0.05). No significant MD or AD difference was observed between groups. Diffusion metrics of several regions significantly correlated with non-motor (state and trait anxiety and daytime sleepiness) and axial motor symptoms in the de novo PD group. No correlations were observed between diffusion metrics and other clinical symptoms evaluated.

Conclusion: Our findings suggest microstructural changes in de novo PD fiber tracts; however, limited associations with clinical symptoms reveal the complexity of PD pathology. They may contribute to understanding the neurobiological changes underlying PD and have implications for developing targeted interventions. However, further longitudinal research with larger cohorts and consideration of confounding factors are necessary to elucidate the underlying mechanisms of these diffusion alterations in de novo PD.

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来源期刊
Neuroradiology
Neuroradiology 医学-核医学
CiteScore
5.30
自引率
3.60%
发文量
214
审稿时长
4-8 weeks
期刊介绍: Neuroradiology aims to provide state-of-the-art medical and scientific information in the fields of Neuroradiology, Neurosciences, Neurology, Psychiatry, Neurosurgery, and related medical specialities. Neuroradiology as the official Journal of the European Society of Neuroradiology receives submissions from all parts of the world and publishes peer-reviewed original research, comprehensive reviews, educational papers, opinion papers, and short reports on exceptional clinical observations and new technical developments in the field of Neuroimaging and Neurointervention. The journal has subsections for Diagnostic and Interventional Neuroradiology, Advanced Neuroimaging, Paediatric Neuroradiology, Head-Neck-ENT Radiology, Spine Neuroradiology, and for submissions from Japan. Neuroradiology aims to provide new knowledge about and insights into the function and pathology of the human nervous system that may help to better diagnose and treat nervous system diseases. Neuroradiology is a member of the Committee on Publication Ethics (COPE) and follows the COPE core practices. Neuroradiology prefers articles that are free of bias, self-critical regarding limitations, transparent and clear in describing study participants, methods, and statistics, and short in presenting results. Before peer-review all submissions are automatically checked by iThenticate to assess for potential overlap in prior publication.
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