Centre for the Developing Brain, Division of Imaging Sciences & Biomedical Engineering, King's College London, St Thomas' Hospital, Westminster Bridge Rd, London SE1 7EH, UK.
Centre for the Developing Brain, Division of Imaging Sciences & Biomedical Engineering, King's College London, St Thomas' Hospital, Westminster Bridge Rd, London SE1 7EH, UK.
Neuroimage. 2014 Nov 1;101:555-68. doi: 10.1016/j.neuroimage.2014.06.074. Epub 2014 Jul 6.
There is growing interest in exploring fetal functional brain development, particularly with Resting State fMRI. However, during a typical fMRI acquisition, the womb moves due to maternal respiration and the fetus may perform large-scale and unpredictable movements. Conventional fMRI processing pipelines, which assume that brain movements are infrequent or at least small, are not suitable. Previous published studies have tackled this problem by adopting conventional methods and discarding as much as 40% or more of the acquired data. In this work, we developed and tested a processing framework for fetal Resting State fMRI, capable of correcting gross motion. The method comprises bias field and spin history corrections in the scanner frame of reference, combined with slice to volume registration and scattered data interpolation to place all data into a consistent anatomical space. The aim is to recover an ordered set of samples suitable for further analysis using standard tools such as Group Independent Component Analysis (Group ICA). We have tested the approach using simulations and in vivo data acquired at 1.5 T. After full motion correction, Group ICA performed on a population of 8 fetuses extracted 20 networks, 6 of which were identified as matching those previously observed in preterm babies.
人们越来越感兴趣地探索胎儿功能性大脑发育,特别是使用静息态 fMRI。然而,在典型的 fMRI 采集过程中,子宫会因母亲的呼吸而移动,并且胎儿可能会进行大规模且不可预测的运动。传统的 fMRI 处理管道假设大脑运动很少或至少很小,因此不适用。以前发表的研究通过采用传统方法并丢弃多达 40%或更多采集的数据来解决这个问题。在这项工作中,我们开发并测试了一种用于胎儿静息态 fMRI 的处理框架,能够纠正大体运动。该方法包括在扫描仪参考系中进行偏置场和自旋历史校正,结合切片到体积配准和离散数据插值,将所有数据放置到一致的解剖空间中。目的是使用标准工具(例如组独立成分分析 (Group ICA))恢复适合进一步分析的有序样本集。我们使用模拟和在 1.5T 下采集的体内数据测试了该方法。在进行完全运动校正后,对 8 名胎儿的群体进行的 Group ICA 提取了 20 个网络,其中 6 个被确定为与先前在早产儿中观察到的网络相匹配。