Diffusion imaging with stimulated echoes: signal models and experiment design
Abstract
Purpose: Stimulated echo acquisition mode (STEAM) diffusion MRI can be advantageous over pulsed-gradient spin-echo (PGSE) for diffusion times that are long compared to . It is important therefore for biomedical diffusion imaging applications at 7T and above where is short. However, imaging gradients in the STEAM sequence contribute much greater diffusion weighting than in PGSE, but are often ignored during post-processing. We demonstrate here that this can severely bias parameter estimates. Method: We present models for the STEAM signal for free and restricted diffusion that account for crusher and slice-select (butterfly) gradients to avoid such bias. The butterfly gradients also disrupt experiment design, typically by skewing gradient-vectors towards the slice direction. We propose a simple compensation to the diffusion gradient vector specified to the scanner that counterbalances the butterfly gradients to preserve the intended experiment design. Results: High-field data fixed from a monkey brain experiments demonstrate the need for both the compensation during acquisition and correct modelling during post-processing for both diffusion tensor imaging and ActiveAx axon-diameter index mapping. Simulations support the results and indicate a similar need in in-vivo human applications. Conclusion: Correct modelling and compensation are important for practical applications of STEAM diffusion MRI.