Benigni Barbara, Ghavasieh Arsham, Corso Alessandra, d'Andrea Valeria, De Domenico Manlio
Department of Information Engineering and Computer Science, University of Trento, Trento, Italy.
CoMuNe Lab, Fondazione Bruno Kessler, Trento, Italy.
Netw Neurosci. 2021 Aug 30;5(3):831-850. doi: 10.1162/netn_a_00203. eCollection 2021.
Information exchange in the human brain is crucial for vital tasks and to drive diseases. Neuroimaging techniques allow for the indirect measurement of information flows among brain areas and, consequently, for reconstructing connectomes analyzed through the lens of network science. However, standard analyses usually focus on a small set of network indicators and their joint probability distribution. Here, we propose an information-theoretic approach for the analysis of synthetic brain networks (based on generative models) and empirical brain networks, and to assess connectome's information capacity at different stages of dementia. Remarkably, our framework accounts for the whole network state, overcoming limitations due to limited sets of descriptors, and is used to probe human connectomes at different scales. We find that the spectral entropy of empirical data lies between two generative models, indicating an interpolation between modular and geometry-driven structural features. In fact, we show that the mesoscale is suitable for characterizing the differences between brain networks and their generative models. Finally, from the analysis of connectomes obtained from healthy and unhealthy subjects, we demonstrate that significant differences between healthy individuals and the ones affected by Alzheimer's disease arise at the microscale (max. posterior probability smaller than 1%) and at the mesoscale (max. posterior probability smaller than 10%).
人类大脑中的信息交流对于维持生命活动和引发疾病至关重要。神经成像技术能够间接测量脑区之间的信息流,进而通过网络科学的视角重建脑连接组。然而,标准分析通常聚焦于一小部分网络指标及其联合概率分布。在此,我们提出一种信息论方法,用于分析合成脑网络(基于生成模型)和实证脑网络,并评估痴呆症不同阶段脑连接组的信息容量。值得注意的是,我们的框架考虑了整个网络状态,克服了因描述符集有限而产生的局限性,并用于在不同尺度上探测人类脑连接组。我们发现实证数据的谱熵介于两个生成模型之间,这表明在模块化和几何驱动的结构特征之间存在插值。事实上,我们表明中尺度适合于表征脑网络与其生成模型之间的差异。最后,通过对健康和不健康受试者的脑连接组分析,我们证明健康个体与受阿尔茨海默病影响的个体之间的显著差异出现在微观尺度(最大后验概率小于1%)和中尺度(最大后验概率小于10%)。