Ouyang Austin, Yu Qiaowen, Mishra Virendra, Chalak Lina, Jeon Tina, Sivarajan Muraleedharan, Jackson Greg, Rollins Nancy, Liu Shuwei, Huang Hao
Advanced Imaging Research Center, University of Texas Southwestern Medical Center, 5323 HarryHines Blvd, Dallas, TX, USA 75390.
Advanced Imaging Research Center, University of Texas Southwestern Medical Center, 5323 HarryHines Blvd, Dallas, TX, USA 75390; Research Center for Sectional and Imaging Anatomy, Shandong University, No 44 West Wenhua Road, Jinan, Shandong, China 250012.
Proc SPIE Int Soc Opt Eng. 2015 Feb 21;9417. doi: 10.1117/12.2082418. Epub 2015 Apr 3.
The structures of developing human brain white matter (WM) tracts can be effectively quantified by DTI-derived metrics, including fractional anisotropy (FA), mean, axial and radial diffusivity (MD, AD and RD). However, dynamics of WM microstructure during very early developmental period from mid-fetal to perinatal stage is unknown. It is difficult to accurately measure microstructural properties of these WM tracts due to severe contamination from cerebrospinal fluid (CSF). In this study, high resolution DTI of fetal brains at mid-fetal stage (20 weeks of gestation or 20wg), 19 brains in the middle of 3 trimester (35wg) and 17 brains around term (40wg) were acquired. We established first population-averaged DTI templates at these three time points and extracted WM skeleton. 16 major WM tracts in limbic, projection, commissural and association tract groups were traced with DTI tractography in native space. The WM skeleton in the template space was inversely transformed back to the native space for measuring core WM microstructures of each individual tract. Continuous microstructural enhancement and volumetric increase of WM tracts were found from 20wg to 40wg. The microstructural enhancement from FA measurement is decelerated in late 3 trimester compared to mid-fetal to middle 3 trimester, while volumetric increase of prefrontal WM tracts is accelerated. The microstructural enhancement from 35wg to 40wg is heterogeneous among different tract groups with microstructures of association tracts undergoing most dramatic change. Besides decreases of RD indicating active myelination, the decrease of AD for most WM tracts during late 3 trimester suggests axonal packing process.
发育中的人类脑白质(WM)束的结构可以通过扩散张量成像(DTI)衍生指标进行有效量化,包括分数各向异性(FA)、平均扩散率、轴向扩散率和径向扩散率(MD、AD和RD)。然而,从胎儿中期到围产期这一非常早期发育阶段的WM微观结构动态尚不清楚。由于脑脊液(CSF)的严重污染,很难准确测量这些WM束的微观结构特性。在本研究中,获取了胎儿中期(妊娠20周或20wg)、妊娠晚期(35wg)的19例胎儿脑和足月(40wg)的17例胎儿脑的高分辨率DTI数据。我们在这三个时间点建立了首个群体平均DTI模板并提取了WM骨架。在原始空间中,利用DTI纤维束成像技术追踪了边缘系统、投射、连合和联合纤维束组中的16条主要WM束。将模板空间中的WM骨架反向变换回原始空间,以测量每条个体纤维束的核心WM微观结构。发现从20wg到40wg,WM束的微观结构持续增强且体积增加。与胎儿中期到妊娠晚期相比,妊娠晚期FA测量的微观结构增强速度减慢,而前额叶WM束的体积增加加速。从35wg到