Radiology Research, Children's Hospital of Philadelphia, Philadelphia, PA 19104.
Advanced Imaging Research Center, University of Texas Southwestern Medical Center, Dallas, TX 75390.
Proc Natl Acad Sci U S A. 2019 Mar 5;116(10):4681-4688. doi: 10.1073/pnas.1812156116. Epub 2019 Feb 19.
During the third trimester, the human brain undergoes rapid cellular and molecular processes that reshape the structural architecture of the cerebral cortex. Knowledge of cortical differentiation obtained predominantly from histological studies is limited in localized and small cortical regions. How cortical microstructure is differentiated across cortical regions in this critical period is unknown. In this study, the cortical microstructural architecture across the entire cortex was delineated with non-Gaussian diffusion kurtosis imaging as well as conventional diffusion tensor imaging of 89 preterm neonates aged 31-42 postmenstrual weeks. The temporal changes of cortical mean kurtosis (MK) or fractional anisotropy (FA) were heterogeneous across the cortical regions. Cortical MK decreases were observed throughout the studied age period, while cortical FA decrease reached its plateau around 37 weeks. More rapid decreases in MK were found in the primary visual region, while faster FA declines were observed in the prefrontal cortex. We found that distinctive cortical microstructural changes were coupled with microstructural maturation of associated white matter tracts. Both cortical MK and FA measurements predicted the postmenstrual age of preterm infants accurately. This study revealed a differential 4D spatiotemporal cytoarchitectural signature inferred by non-Gaussian diffusion barriers inside the cortical plate during the third trimester. The cytoarchitectural processes, including dendritic arborization and neuronal density decreases, were inferred by regional cortical FA and MK measurements. The presented findings suggest that cortical MK and FA measurements could be used as effective imaging markers for cortical microstructural changes in typical and potentially atypical brain development.
在妊娠晚期,人类大脑经历快速的细胞和分子过程,重塑大脑皮层的结构架构。主要通过组织学研究获得的皮质分化知识在局部和小的皮质区域是有限的。在这个关键时期,皮质微结构如何在整个皮质区域分化尚不清楚。在这项研究中,使用非高斯扩散峰度成像以及 89 名胎龄为 31-42 周的早产儿的常规扩散张量成像,描绘了整个皮层的皮质微观结构架构。皮质平均峰度(MK)或各向异性分数(FA)的时间变化在皮质区域是不均匀的。在整个研究年龄期间观察到皮质 MK 降低,而皮质 FA 降低在 37 周左右达到平台期。在初级视觉区域观察到 MK 更快的降低,而在前额叶皮层观察到更快的 FA 下降。我们发现,独特的皮质微观结构变化与相关白质束的微观结构成熟有关。皮质 MK 和 FA 测量均能准确预测早产儿的胎龄。本研究揭示了妊娠晚期皮质板内非高斯扩散障碍推断的皮质结构的差异 4D 时空细胞架构特征。通过区域皮质 FA 和 MK 测量推断出细胞架构过程,包括树突分支和神经元密度的降低。研究结果表明,皮质 MK 和 FA 测量可作为皮质微观结构变化的有效成像标志物,用于典型和潜在非典型脑发育。