不同帕金森病运动亚型脑容量和皮质下髓磷脂的合成MRI研究

IF 8.2 1区 医学 Q1 NEUROSCIENCES
Dongliang Cheng, Junyan Wen, Nan Ding, Zhenpeng Duan, Biqing Lin, Yunjun Yang, Yaozhong Wu, Hang Wang, Jincheng Ma, Jialu Zhang, Zhifeng Xu, Hai Zhao, Yulin Liu, Ge Wen
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引用次数: 0

摘要

震颤主导型(TD)和姿势不稳定和步态困难型(PIGD)帕金森病亚型之间脑容量和皮质下髓磷脂含量(MyC)的变化尚不清楚。本研究利用合成MRI研究了PD运动亚型的全脑容量和皮质下髓磷脂含量的差异。纳入92例PD患者(TD 39例,PIGD 53例)和39例健康对照。ANCOVA发现PD患者表现出灰质、白质和MyC减少,TD和PIGD之间没有明显的萎缩模式。大多数皮质下核髓磷脂减少,而PIGD表现出更广泛的改变,双侧尾状髓磷脂增加;TD表现出不对称的丘脑髓磷脂变化,呈偏侧增减。在TD和PIGD之间观察到左侧尾状核和右侧GPi的MyC显著差异。合成mri衍生参数提供了PD全脑萎缩模式和髓磷脂动态变化的见解,有助于更深入地了解PD亚型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Synthetic MRI study of brain volume and subcortical myelin in various Parkinson’s disease motor subtypes

Synthetic MRI study of brain volume and subcortical myelin in various Parkinson’s disease motor subtypes

Alterations in brain volume and subcortical myelin content (MyC) between tremor-dominant (TD) and postural instability and gait difficulty (PIGD) subtypes of Parkinson’s (PD) disease remain unclear. This study investigated whole-brain volume and subcortical myelin content differences among PD motor subtypes using synthetic MRI. Ninety-two PD patients (39 TD and 53 PIGD) and 39 healthy controls were included. ANCOVA identified that PD patients exhibited reduced gray matter, white matter, and MyC, with no distinct atrophy patterns between TD and PIGD. Most subcortical nuclei showed decreased myelin, while PIGD presented more extensive alterations and increased bilateral caudate myelin; TD exhibited asymmetric thalamic myelin changes, with lateralized increases and decreases. Significant MyC differences in the left caudate and right GPi were observed between TD and PIGD. Synthetic MRI-derived parameters provide insights into whole-brain atrophy patterns and dynamic myelin changes in PD, contributing to a deeper understanding of PD subtypes.

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来源期刊
NPJ Parkinson's Disease
NPJ Parkinson's Disease Medicine-Neurology (clinical)
CiteScore
9.80
自引率
5.70%
发文量
156
审稿时长
11 weeks
期刊介绍: npj Parkinson's Disease is a comprehensive open access journal that covers a wide range of research areas related to Parkinson's disease. It publishes original studies in basic science, translational research, and clinical investigations. The journal is dedicated to advancing our understanding of Parkinson's disease by exploring various aspects such as anatomy, etiology, genetics, cellular and molecular physiology, neurophysiology, epidemiology, and therapeutic development. By providing free and immediate access to the scientific and Parkinson's disease community, npj Parkinson's Disease promotes collaboration and knowledge sharing among researchers and healthcare professionals.
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