Related Experiment Video
Updated: Jan 15, 2026

Diffusion Imaging in the Rat Cervical Spinal Cord
Published on: April 7, 2015
Correcting unwanted diffusion weighting in diffusion-weighted-STEAM sequence for time-dependent diffusion kurtosis
Qinfeng Zhu1, Ruichen Ba1, Zuozhen Cao1
1Department of Biomedical Engineering, College of Biomedical Engineering & Instrument Science, Zhejiang University, Hangzhou, China.
Purpose:
This study proposes an optimized acquisition protocol to minimize the unwanted diffusion weighting in DW-STEAM and facilitate time-dependent diffusion kurtosis imaging (tDKI).
Methods:
We first corrected the diffusion-direction-dependent shift by optimizing the diffusion gradient amplitude. We then proposed to use low-b-value in the reference image, instead of the conventional non-diffusion-weighted (b0) acquisition, and removed the crusher gradients. The tDKI measurements from the proposed strategy were compared with conventional DWIs that included crushers in the b0 image, in a water phantom and in healthy adults (n = 8) on 3 T, and the water exchange time (τex) was calculated from the tDKI measurements. The optimal strategy was tested in five ex vivo human brains, and the results were compared with in vivo data.
Results:
Neglecting the diffusion weighting in b0 images introduced an artificial time dependence in the apparent diffusivity of the water phantom, and resulted in elevated estimates of water exchange time (τex) in in the in vivo data. Additionally, the AIC indicated that, even when diffusion weighting in the b0 images was accounted for, the kurtosis estimation remained less stable in the in vivo than with the crusher-free approach. In contrast, using low-b-value images as reference measurements yielded reasonable tDKI estimates, with τex ranging from 15 to 40 ms for gray matter in vivo and from 20 to 60 ms for gray matter ex vivo.
Conclusions:
The optimized DW-STEAM acquisition eliminated artificial diffusion-time dependence, enabling the acquisition of accurate tDKI data for mapping structural morphology and transmembrane permeability.

