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Longitudinal Connectome-based Predictive Modeling for REM Sleep Behavior Disorder from Structural Brain Connectivity

机译:基于纵向连接体的REM睡眠行为从结构性脑连接性的预测模型。

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Methods to identify nouroplasticity patterns in human brains arc of the utmost importance in understanding and potentially treating neurodegenerative diseases. Parkinson disease (PD) research will greatly benefit and advance from the discovery of biomarkers to quantify brain changes in the early stages of the disease, a prodromal period when subjects show no obvious clinical symptoms. Diffusion tensor imaging (DTI) allows for an in-vivo estimation of the structural connectome inside the brain and may serve to quantify the degenerative process before the appearance of clinical symptoms. In this work, we introduce a novel strategy to compute longitudinal structural connectomes in the context of a whole-brain data-driven pipeline. In these initial tests, we show that our predictive models are able to distinguish controls from asymptomatic subjects at high risk of developing PD (REM sleep behavior disorder, RBD) with an area under the receiving operating characteristic curve of 0.90 (p<0.001) and a longitudinal dataset of 46 subjects part of the Parkinson's Progression Markers Initiative. By analyzing the brain connections most relevant for the predictive ability of the best performing model, we find connections that are biologically relevant to the disease.
机译:识别人脑中的神经可塑性模式的方法对于理解和潜在治疗神经退行性疾病至关重要。帕金森病(PD)研究将大大受益于生物标志物的发现并从中发展,以量化疾病早期阶段的脑部变化,这是受试者没有明显临床症状的前驱时期。扩散张量成像(DTI)可以对大脑内部的结构连接体进行体内评估,并且可以在临床症状出现之前量化退化过程。在这项工作中,我们介绍了一种在全脑数据驱动管道的背景下计算纵向结构连接体的新颖策略。在这些初始测试中,我们证明了我们的预测模型能够将对照组与处于发生PD(REM睡眠行为障碍,RBD)高风险的无症状受试者区分开,该区的接收操作特征曲线下面积为0.90(p <0.001),并且纵向数据集,其中包含46个主题,是帕金森氏症发展计划的一部分。通过分析与最佳表现模型的预测能力最相关的大脑联系,我们发现与该疾病生物学相关的联系。

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