Co-evolution of Functional Brain Network at Multiple Scales during Early Infancy

The human brains are organized into hierarchically modular networks facilitating efficient and stable information processing and supporting diverse cognitive processes during the course of development. While the remarkable reconfiguration of functional brain network has been firmly established in early life, all these studies investigated the network development from a "single-scale" perspective, which ignore the richness engendered by its hierarchical nature. To fill this gap, this paper leveraged a longitudinal infant resting-state functional magnetic resonance imaging dataset from birth to 2 years of age, and proposed an advanced methodological framework to delineate the multi-scale reconfiguration of functional brain network during early development. Our proposed framework is consist of two parts. The first part developed a novel two-step multi-scale module detection method that could uncover efficient and consistent modular structure for longitudinal dataset from multiple scales in a completely data-driven manner. The second part designed a systematic approach that employed the linear mixed-effect model to four global and nodal module-related metrics to delineate scale-specific age-related changes of network organization. By applying our proposed methodological framework on the collected longitudinal infant dataset, we provided the first evidence that, in the first 2 years of life, the brain functional network is co-evolved at different scales, where each scale displays the unique reconfiguration pattern in terms of modular organization.

[1]  Gang Pan,et al.  Multi-layer Temporal Network Analysis Reveals Increasing Temporal Reachability and Spreadability in the First Two Years of Life , 2019, MICCAI.

[2]  Alan C. Evans,et al.  Uncovering Intrinsic Modular Organization of Spontaneous Brain Activity in Humans , 2009, PloS one.

[3]  Abraham Z. Snyder,et al.  Spurious but systematic correlations in functional connectivity MRI networks arise from subject motion , 2012, NeuroImage.

[4]  R. Guimerà,et al.  Functional cartography of complex metabolic networks , 2005, Nature.

[5]  Xenophon Papademetris,et al.  Groupwise whole-brain parcellation from resting-state fMRI data for network node identification , 2013, NeuroImage.

[6]  John H. Gilmore,et al.  Imaging structural and functional brain development in early childhood , 2018, Nature Reviews Neuroscience.

[7]  Danielle S. Bassett,et al.  Multi-scale brain networks , 2016, NeuroImage.

[8]  Denise C. Park,et al.  Decreased segregation of brain systems across the healthy adult lifespan , 2014, Proceedings of the National Academy of Sciences.

[9]  Dinggang Shen,et al.  Multi-layer Large-Scale Functional Connectome Reveals Infant Brain Developmental Patterns , 2018, MICCAI.

[10]  Alex Arenas,et al.  Analysis of the structure of complex networks at different resolution levels , 2007, physics/0703218.

[11]  Andrea Lancichinetti,et al.  Benchmarks for testing community detection algorithms on directed and weighted graphs with overlapping communities. , 2009, Physical review. E, Statistical, nonlinear, and soft matter physics.

[12]  Mason A. Porter,et al.  Robust Detection of Dynamic Community Structure in Networks , 2012, Chaos.

[13]  Dinggang Shen,et al.  Temporal and Spatial Evolution of Brain Network Topology during the First Two Years of Life , 2011, PloS one.

[14]  Edward T. Bullmore,et al.  Modular and Hierarchically Modular Organization of Brain Networks , 2010, Front. Neurosci..

[15]  Dinggang Shen,et al.  Test-Retest Reliability of “High-Order” Functional Connectivity in Young Healthy Adults , 2017, Front. Neurosci..

[16]  Olaf Sporns,et al.  Functional brain modules reconfigure at multiple scales across the human lifespan , 2015, 1510.08045.

[17]  Dinggang Shen,et al.  First-year development of modules and hubs in infant brain functional networks , 2019, NeuroImage.

[18]  Jean-Loup Guillaume,et al.  Fast unfolding of communities in large networks , 2008, 0803.0476.