4.7 Article

Scattered slice SHARD reconstruction for motion correction in multi-shell diffusion MRI

期刊

NEUROIMAGE
卷 225, 期 -, 页码 -

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.neuroimage.2020.117437

关键词

Diffusion MRI; Multi-shell; Motion correction; Slice-to-volume reconstruction; Neonatal imaging

资金

  1. European Research Council under the European Union [319456]
  2. MRC strategic funds [MR/K006355/1]
  3. Flemish Research Foundation (FWO) [12ZV420N]
  4. Wellcome Trust Fellowship [WT/201374/Z/16/Z]
  5. Wellcome/EPSRC Centre for Medical Engineering at King's College London [WT/203148/Z/16/Z]
  6. National Institute for Health Research (NIHR) Biomedical Research Centre at Guy's and St Thomas' NHS Foundation Trust and King's College London
  7. MRC [MR/K006355/1] Funding Source: UKRI

向作者/读者索取更多资源

Diffusion MRI provides valuable insights into neural microstructure and connectivity in the developing brain. This study introduces a reconstruction method for scattered slice multi-shell HARDI data, enabling accurate motion correction and reconstruction even in severely motion-corrupted subjects. The framework integrates various techniques such as slice-level outlier rejection, distortion correction, and data-driven representation, showing promise for future microstructure imaging research.
Diffusion MRI offers a unique probe into neural microstructure and connectivity in the developing brain. However, analysis of neonatal brain imaging data is complicated by inevitable subject motion, leading to a series of scattered slices that need to be aligned within and across diffusion-weighted contrasts. Here, we develop a reconstruction method for scattered slice multi-shell high angular resolution diffusion imaging (HARDI) data, jointly estimating an uncorrupted data representation and motion parameters at the slice or multiband excitation level. The reconstruction relies on data-driven representation of multi-shell HARDI data using a bespoke spherical harmonics and radial decomposition (SHARD), which avoids imposing model assumptions, thus facilitating to compare various microstructure imaging methods in the reconstructed output. Furthermore, the proposed framework integrates slice-level outlier rejection, distortion correction, and slice profile correction. We evaluate the method in the neonatal cohort of the developing Human Connectome Project (650 scans). Validation experiments demonstrate accurate slice-level motion correction across the age range and across the range of motion in the population. Results in the neonatal data show successful reconstruction even in severely motion-corrupted subjects. In addition, we illustrate how local tissue modelling can extract advanced microstructure features such as orientation distribution functions from the motion-corrected reconstructions.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据