Abstract

PurposeDiffusion‐weighted steady‐state free precession (DW‐SSFP) is shown to provide a means to probe non‐Gaussian diffusion through manipulation of the flip angle. A framework is presented to define an effective b‐value in DW‐SSFP.TheoryThe DW‐SSFP signal is a summation of coherence pathways with different b‐values. The relative contribution of each pathway is dictated by the flip angle. This leads to an apparent diffusion coefficient (ADC) estimate that depends on the flip angle in non‐Gaussian diffusion regimes. By acquiring DW‐SSFP data at multiple flip angles and modeling the variation in ADC for a given form of non‐Gaussianity, the ADC can be estimated at a well‐defined effective b‐value.MethodsA gamma distribution is used to model non‐Gaussian diffusion, embedded in the Buxton signal model for DW‐SSFP. Monte‐Carlo simulations of non‐Gaussian diffusion in DW‐SSFP and diffusion‐weighted spin‐echo sequences are used to verify the proposed framework. Dependence of ADC on flip angle in DW‐SSFP is verified with experimental measurements in a whole, human postmortem brain.ResultsMonte‐Carlo simulations reveal excellent agreement between ADCs estimated with diffusion‐weighted spin‐echo and the proposed framework. Experimental ADC estimates vary as a function of flip angle over the corpus callosum of the postmortem brain, estimating the mean and standard deviation of the gamma distribution as 1.50·10-4 mm2/s and 2.10·10-4 mm2/s.ConclusionDW‐SSFP can be used to investigate non‐Gaussian diffusion by varying the flip angle. By fitting a model of non‐Gaussian diffusion, the ADC in DW‐SSFP can be estimated at an effective b‐value, comparable to more conventional diffusion sequences.

Highlights

  • Diffusion-weighted steady-state free precession (DW-SSFP) is a powerful sequence that achieves strong diffusion weighting by maintaining a steady-state in which magnetization accumulates diffusion contrast over multiple repetition times (TRs).[1-4]

  • As diffusive motion in tissue is generally non-Gaussian, this poorlydefined b-value prevents comparisons between diffusivity estimates obtained with the DW-SSFP and more conventional measurements using the diffusion-weighted spin-echo (DW-SE) sequence (Figure 1B)

  • We propose a method to translate quantitative diffusivity estimates derived with DW-SSFP, in which b-values are not well defined, into apparent diffusion coefficient (ADC) estimates at a single effective b-value, as would be measured using more conventional sequences such as DW-SE

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Summary

Funding information

Purpose: Diffusion-weighted steady-state free precession (DW-SSFP) is shown to provide a means to probe non-Gaussian diffusion through manipulation of the flip angle. The relative contribution of each pathway is dictated by the flip angle This leads to an apparent diffusion coefficient (ADC) estimate that depends on the flip angle in non-Gaussian diffusion regimes. By acquiring DW-SSFP data at multiple flip angles and modeling the variation in ADC for a given form of non-Gaussianity, the ADC can be estimated at a well-defined effective b-value. Monte-Carlo simulations of non-Gaussian diffusion in DW-SSFP and diffusion-weighted spin-echo sequences are used to verify the proposed framework. Results: Monte-Carlo simulations reveal excellent agreement between ADCs estimated with diffusion-weighted spin-echo and the proposed framework. KEYWORDS b-value, diffusion-weighted spin-echo, diffusion-weighted steady-state free precession, Monte-Carlo, non-Gaussian diffusion, postmortem MRI.

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