Modeling Functional Dynamics of Cortical Gyri and Sulci

Cortical gyrification is one of the most prominent features of human brain. A variety of studies in the brain mapping field have demonstrated the specific structural and functional differences between gyral and sulcal regions. However, previous studies of gyri/sulci function analysis based on the fMRI data assume the temporal stationarity over the entire fMRI scan, while the possible temporal dynamics of gyri/sulci function is largely unknown. We present a computational framework to model the functional dynamics of cortical gyri and sulci based on task fMRI data. Specifically, the whole-brain fMRI signals’ temporal segments are derived via the sliding time window approach. The spatial overlap patterns among functional networks (SOPFNs), which are crucial for characterizing brain functions, are then measured within each time window via a group-wise sparse representation approach. Finally, the temporal dynamics of SOPFNs distribution on gyral/sulcal regions across all time windows are assessed. Experimental results based on the publicly released Human Connectome Project task fMRI data demonstrated that the proposed framework identified meaningful temporal dynamics difference of the SOPFNs distribution between gyral and sulcal regions which are reproducible across different subjects and task fMRI datasets. Our results provide novel understanding of functional dynamics mechanisms of human cerebral cortex.

[1]  Tuo Zhang,et al.  A functional model of cortical gyri and sulci , 2013, Brain Structure and Function.

[2]  Guillermo Sapiro,et al.  Online Learning for Matrix Factorization and Sparse Coding , 2009, J. Mach. Learn. Res..

[3]  J. Duncan The multiple-demand (MD) system of the primate brain: mental programs for intelligent behaviour , 2010, Trends in Cognitive Sciences.

[4]  Dajiang Zhu,et al.  Dynamic functional connectomics signatures for characterization and differentiation of PTSD patients , 2014, Human brain mapping.

[5]  P. Rakic Specification of cerebral cortical areas. , 1988, Science.

[6]  Sungho Tak,et al.  A Data-Driven Sparse GLM for fMRI Analysis Using Sparse Dictionary Learning With MDL Criterion , 2011, IEEE Transactions on Medical Imaging.

[7]  Jieping Ye,et al.  Holistic Atlases of Functional Networks and Interactions Reveal Reciprocal Organizational Architecture of Cortical Function , 2015, IEEE Transactions on Biomedical Engineering.

[8]  C. Gilbert,et al.  Brain States: Top-Down Influences in Sensory Processing , 2007, Neuron.

[9]  Xiaoping P. Hu,et al.  Coevolution of gyral folding and structural connection patterns in primate brains. , 2013, Cerebral cortex.

[10]  Jinglei Lv,et al.  Sparse representation of HCP grayordinate data reveals novel functional architecture of cerebral cortex , 2015, Human brain mapping.

[11]  Dinggang Shen,et al.  Axonal fiber terminations concentrate on gyri. , 2012, Cerebral cortex.

[12]  Stephen M Smith,et al.  Correspondence of the brain's functional architecture during activation and rest , 2009, Proceedings of the National Academy of Sciences.

[13]  J. Lv,et al.  Assessing effects of prenatal alcohol exposure using group-wise sparse representation of fMRI data , 2015, Psychiatry Research: Neuroimaging.

[14]  Emi Takahashi,et al.  Emerging cerebral connectivity in the human fetal brain: an MR tractography study. , 2012, Cerebral Cortex.

[15]  Heng Huang,et al.  Sparse representation of whole-brain fMRI signals for identification of functional networks , 2015, Medical Image Anal..

[16]  Mark Jenkinson,et al.  The minimal preprocessing pipelines for the Human Connectome Project , 2013, NeuroImage.