帕金森病的代谢网络连接紊乱:一种新的成像生物标记。

IF 2.9 2区 医学 Q2 NEUROSCIENCES
Bei Chen, Xiran Chen, Liling Peng, Shiqi Liu, Yongxiang Tang, Xin Gao
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引用次数: 0

摘要

帕金森病(PD)的诊断一直是个难题。18F-脱氧葡萄糖正电子发射断层扫描(18F-FDG PET)等成像技术的进步突显了帕金森病的代谢改变,但代谢连接组内的动态网络交互作用仍然难以捉摸。为此,我们研究了由 49 名帕金森病患者和 49 名健康对照者组成的数据集。通过采用个性化代谢连接组方法,我们使用标准摄取值(SUV)和詹森-香农发散相似性估计(JSSE)评估了网络内和网络间的连接性。利用随机森林算法确定了区分帕金森病与健康状态的关键神经影像特征。具体而言,研究结果表明,帕金森病患者的网络连接性增强,特别是在躯体运动(SMN)和额顶叶(FPN)网络中,经多重比较校正后,帕金森病患者的网络连接性仍持续存在(P<0.05)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Metabolic network connectivity disturbances in Parkinson's disease: a novel imaging biomarker.

The diagnosis of Parkinson's Disease (PD) presents ongoing challenges. Advances in imaging techniques like 18F-fluorodeoxyglucose positron emission tomography (18F-FDG PET) have highlighted metabolic alterations in PD, yet the dynamic network interactions within the metabolic connectome remain elusive. To this end, we examined a dataset comprising 49 PD patients and 49 healthy controls. By employing a personalized metabolic connectome approach, we assessed both within- and between-network connectivities using Standard Uptake Value (SUV) and Jensen-Shannon Divergence Similarity Estimation (JSSE). A random forest algorithm was utilized to pinpoint key neuroimaging features differentiating PD from healthy states. Specifically, the results revealed heightened internetwork connectivity in PD, specifically within the somatomotor (SMN) and frontoparietal (FPN) networks, persisting after multiple comparison corrections (P < 0.05, Bonferroni adjusted for 10% and 20% sparsity). This altered connectivity effectively distinguished PD patients from healthy individuals. Notably, this study utilizes 18F-FDG PET imaging to map individual metabolic networks, revealing enhanced connectivity in the SMN and FPN among PD patients. This enhanced connectivity may serve as a promising imaging biomarker, offering a valuable asset for early PD detection.

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来源期刊
Cerebral cortex
Cerebral cortex 医学-神经科学
CiteScore
6.30
自引率
8.10%
发文量
510
审稿时长
2 months
期刊介绍: Cerebral Cortex publishes papers on the development, organization, plasticity, and function of the cerebral cortex, including the hippocampus. Studies with clear relevance to the cerebral cortex, such as the thalamocortical relationship or cortico-subcortical interactions, are also included. The journal is multidisciplinary and covers the large variety of modern neurobiological and neuropsychological techniques, including anatomy, biochemistry, molecular neurobiology, electrophysiology, behavior, artificial intelligence, and theoretical modeling. In addition to research articles, special features such as brief reviews, book reviews, and commentaries are included.
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