Xia Jing, Zhang Caiming, Wang Fan, Benkarim Oualid M, Sanroma Gerard, Piella Gemma, González Balleste Miguel A, Hahner Nadine, Eixarch Elisenda, Shen Dinggang, Li Gang
Department of Computer Science and Technology, Shandong University, Shandong, China.
Department of Radiology and BRIC, University of North Carolina at Chapel Hill, NC 27599, USA.
Proc IEEE Int Symp Biomed Imaging. 2018 Apr;2018:696-699. doi: 10.1109/ISBI.2018.8363669. Epub 2018 May 24.
Dividing the human cerebral cortex into structurally and functionally distinct regions is important in many neuroimaging studies. Although many parcellations have been created for adults, they are not applicable for fetal studies, due to dramatic differences in brain size, shape and folding between adults and fetuses, as well as dynamic growth of fetal brains. To address this issue, we propose a novel method to divide a population of fetal cortical surfaces into distinct regions based on the dynamic growth patterns of cortical properties, which indicate the underlying changes of microstructures. As microstructures determine the molecular organization and functional principles of the cortex, growth patterns enable an accurate definition of distinct regions in development, microstructure, and function. To comprehensively capture the similarities of cortical growth patterns among vertices, we construct two complementary similarity matrices. One is directly based on the growth trajectories of vertices and the other is based on the correlation profiles of vertices' growth trajectories in relation to those of reference points. Then, we nonlinearly fuse these two similarity matrices into a single one, which can better captures both their common and complementary information than by simply averaging them. Finally, based on this fused matrix, we perform spectral clustering to divide fetal cortical surfaces into distinct regions. We have applied our method on 25 normal fetuses from 26 to 29 gestational weeks and generated biologically meaningful parcellations.
在许多神经影像学研究中,将人类大脑皮层划分为结构和功能上不同的区域非常重要。尽管已经为成年人创建了许多脑区划分方法,但由于成年人和胎儿在大脑大小、形状和折叠方式上存在显著差异,以及胎儿大脑的动态生长,这些方法不适用于胎儿研究。为了解决这个问题,我们提出了一种新方法,根据皮层属性的动态生长模式将胎儿皮层表面群体划分为不同区域,这些生长模式指示了微观结构的潜在变化。由于微观结构决定了皮层的分子组织和功能原理,生长模式能够在发育、微观结构和功能方面准确地定义不同区域。为了全面捕捉顶点之间皮层生长模式的相似性,我们构建了两个互补的相似性矩阵。一个直接基于顶点的生长轨迹,另一个基于顶点生长轨迹与参考点生长轨迹的相关性剖面。然后,我们将这两个相似性矩阵非线性融合为一个单一矩阵,与简单平均相比,它能更好地捕捉它们的共同和互补信息。最后,基于这个融合矩阵,我们进行谱聚类,将胎儿皮层表面划分为不同区域。我们已将我们的方法应用于25例孕26至29周的正常胎儿,并生成了具有生物学意义的脑区划分。