Validation study demonstrates rapid acquisition of time-dependent diffusion MRI in human brain and prostate, indicating a time-efficient method for tissue microstructure imaging.
Purpose To develop a time‐efficient pulse sequence that acquires multiple diffusion‐weighted images with distinct diffusion times in a single shot by using multiple stimulated echoes (mSTE) with variable flip angles (VFA). Methods The proposed diffusion‐weighted mSTE with VFA (DW‐mSTE‐VFA) sequence begins with two 90° RF pulses that straddle a diffusion gradient lobe ( G D ) to excite and restore one half of the magnetization into the longitudinal axis. The restored longitudinal magnetization was successively re‐excited by a series of RF pulses with VFA, each followed by another G D , to generate a set of stimulated echoes. Each of the multiple stimulated echoes was acquired with an EPI echo train. As such, the train of multiple stimulated echoes produced a set of diffusion‐weighted images with varying diffusion times in a single shot. This technique was experimentally demonstrated on a diffusion phantom, a fruit, and healthy human brain and prostate at 3 T. Results In the phantom experiment, the mean ADC measured at different diffusion times using DW‐mSTE‐VFA were highly consistent (r = 0.999) with those from a commercial spin‐echo diffusion‐weighted EPI sequence. In the fruit and brain experiments, DW‐mSTE‐VFA exhibited similar diffusion‐time dependence to a standard diffusion‐weighted stimulated echo sequence. The ADC showed significant time dependence in the human brain ( p = 0.003 in both white matter and gray matter) and prostate tissues ( p = 0.003 in both peripheral zone and central gland). Conclusion DW‐mSTE‐VFA offers a time‐efficient tool for investigating the diffusion‐time dependency in diffusion MRI studies.
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Dan et al. (2023) studied this question.
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