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Purpose  Oscillating gradient spin‐echo (OGSE) sequences have demonstrated an ability to probe time‐dependent microstructural features, although they often suffer from low SNR due to increased TEs. In this work we introduce frequency‐tuned bipolar (FTB) gradients as a variation of oscillating gradients with reduced TE and demonstrate their utility by mapping the frequency dispersion of kurtosis in human subjects.    Methods  An FTB oscillating gradient waveform is presented that provides encoding of 1.5 net oscillation periods, thereby reducing the TE of the acquisition. Simulations were performed to determine an optimal protocol based on the SNR of kurtosis frequency dispersion—defined as the difference in kurtosis between pulsed and oscillating gradient acquisitions. Healthy human subjects were scanned at 7T using pulsed gradient and an optimized 23 Hz FTB protocol, which featured a maximum  b ‐value of 2500 s/mm 2 . In addition, to directly compare existing methods, measurements using traditional cosine OGSE were also acquired.    Results  FTB oscillating gradients demonstrated equivalent frequency‐dependent diffusion measurements compared with cosine‐modulated OGSE while enabling a significant reduction in TE. Optimization and in vivo results suggest that FTB gradients provide increased SNR of kurtosis dispersion maps compared with traditional cosine OGSE. The optimized FTB gradient protocol demonstrated consistent reductions in apparent kurtosis values and increased diffusivity in generated frequency dispersion maps.    Conclusions  This work presents an alternative to traditional cosine OGSE sequences, enabling more time‐efficient acquisitions of frequency‐dependent diffusion quantities as demonstrated through in vivo kurtosis frequency dispersion maps.

Tuned bipolar oscillating gradients for mapping frequency dispersion of diffusion kurtosis in the human brain