Rahim Mehdi, Thirion Bertrand, Comtat Claude, Varoquaux Gaël
Parietal project team - INRIA Saclay and with IMIV team - CEA Saclay DRF/I2BM/NeuroSpin and SHFJ. Paris-Saclay University. France.
Parietal project team - INRIA Saclay and CEA Saclay DRF/I2BM/NeuroSpin. Paris-Saclay University. France.
IEEE J Sel Top Signal Process. 2016 Oct;10(7):120-1213. doi: 10.1109/JSTSP.2016.2600400. Epub 2016 Aug 15.
Functional connectivity describes neural activity from resting-state functional magnetic resonance imaging (rs-fMRI). This noninvasive modality is a promising imaging biomarker of neurodegenerative diseases, such as Alzheimer's disease (AD), where the connectome can be an indicator to assess and to understand the pathology. However, it only provides noisy measurements of brain activity. As a consequence, it has shown fairly limited discrimination power on clinical groups. So far, the reference functional marker of AD is the fluorodeoxyglucose positron emission tomography (FDG-PET). It gives a reliable quantification of metabolic activity, but it is costly and invasive. Here, our goal is to analyze AD populations solely based on rs-fMRI, as functional connectivity is correlated to metabolism. We introduce : leveraging a prior from one modality to improve results of another modality on different subjects. A metabolic prior is learned from an independent FDG-PET dataset to improve functional connectivity-based prediction of AD. The prior acts as a regularization of connectivity learning and improves the estimation of discriminative patterns from distinct rs-fMRI datasets. Our approach is a two-stage classification strategy that combines several seed-based connectivity maps to cover a large number of functional networks that identify AD physiopathology. Experimental results show that our transmodal approach increases classification accuracy compared to pure rs-fMRI approaches, without resorting to additional invasive acquisitions. The method successfully recovers brain regions known to be impacted by the disease.
功能连接性描述了静息态功能磁共振成像(rs-fMRI)中的神经活动。这种非侵入性模态是神经退行性疾病(如阿尔茨海默病(AD))的一种很有前景的成像生物标志物,在AD中,连接组可以作为评估和理解病理的一个指标。然而,它只能提供大脑活动的噪声测量。因此,它在临床组上的鉴别能力相当有限。到目前为止,AD的参考功能标志物是氟脱氧葡萄糖正电子发射断层扫描(FDG-PET)。它能可靠地量化代谢活动,但成本高昂且具有侵入性。在这里,我们的目标是仅基于rs-fMRI分析AD人群,因为功能连接性与代谢相关。我们引入:利用一种模态的先验信息来改善不同受试者上另一种模态的结果。从一个独立的FDG-PET数据集中学习代谢先验信息,以改善基于功能连接性的AD预测。该先验作为连接性学习的正则化,并改善了从不同rs-fMRI数据集中对鉴别模式的估计。我们的方法是一种两阶段分类策略,它结合了几个基于种子的连接性图谱,以覆盖大量识别AD生理病理学的功能网络。实验结果表明,与纯rs-fMRI方法相比,我们的跨模态方法提高了分类准确率,而无需借助额外的侵入性采集。该方法成功地恢复了已知受该疾病影响的脑区。