Department of Biomedical Engineering, Washington University in St. Louis, St. Louis, MO 63130;
Department of Computer Science, Imperial College London, London SW7 2AZ, United Kingdom.
Proc Natl Acad Sci U S A. 2018 Mar 20;115(12):3156-3161. doi: 10.1073/pnas.1715451115. Epub 2018 Mar 5.
During the third trimester of human brain development, the cerebral cortex undergoes dramatic surface expansion and folding. Physical models suggest that relatively rapid growth of the cortical gray matter helps drive this folding, and structural data suggest that growth may vary in both space (by region on the cortical surface) and time. In this study, we propose a unique method to estimate local growth from sequential cortical reconstructions. Using anatomically constrained multimodal surface matching (aMSM), we obtain accurate, physically guided point correspondence between younger and older cortical reconstructions of the same individual. From each pair of surfaces, we calculate continuous, smooth maps of cortical expansion with unprecedented precision. By considering 30 preterm infants scanned two to four times during the period of rapid cortical expansion (28-38 wk postmenstrual age), we observe significant regional differences in growth across the cortical surface that are consistent with the emergence of new folds. Furthermore, these growth patterns shift over the course of development, with noninjured subjects following a highly consistent trajectory. This information provides a detailed picture of dynamic changes in cortical growth, connecting what is known about patterns of development at the microscopic (cellular) and macroscopic (folding) scales. Since our method provides specific growth maps for individual brains, we are also able to detect alterations due to injury. This fully automated surface analysis, based on tools freely available to the brain-mapping community, may also serve as a useful approach for future studies of abnormal growth due to genetic disorders, injury, or other environmental variables.
在人类大脑发育的第三个 trimester,大脑皮层经历了显著的表面扩张和折叠。物理模型表明,皮质灰质的相对快速增长有助于推动这种折叠,结构数据表明,增长可能在空间(皮质表面的区域)和时间上都有所不同。在这项研究中,我们提出了一种独特的方法,从连续的皮质重建中估计局部增长。使用解剖学约束的多模态曲面匹配(aMSM),我们在同一个人的年轻和年长皮质重建之间获得了准确的、受物理指导的点对应关系。从每一对曲面中,我们计算出具有前所未有的精度的皮质扩张连续、平滑的映射。通过考虑 30 名早产儿在快速皮质扩张期间(胎龄 28-38 周)被扫描两次到四次,我们观察到皮质表面上的生长存在显著的区域差异,这与新褶皱的出现一致。此外,这些生长模式在发育过程中发生变化,未受伤的受试者遵循高度一致的轨迹。这些信息提供了皮质生长动态变化的详细图片,将已知的微观(细胞)和宏观(折叠)尺度上的发育模式联系起来。由于我们的方法为个体大脑提供了特定的生长图谱,我们还能够检测到因损伤而导致的变化。这种基于大脑图谱社区免费提供的工具的全自动曲面分析,也可能成为未来研究遗传疾病、损伤或其他环境变量引起的异常生长的有用方法。