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Purpose: ECG and respiratory-gated preclinical cardiac CEST-MRI acquisitions are difficult due to variable saturation recovery with T1, RF interference in the ECG signal, and offset-to-offset variation in Z-magnetization and cardiac phase introduced by changes in cardiac frequency and trigger delays. Methods: The proposed method consists of segmented saturation modules with radial FLASH readouts and golden angle progression. The segmented saturation blocks drive the system to steady-state, and because center k-space is sampled repeatedly, steady-state saturation dominates contrast during gridding and reconstruction. Ten complete Z-spectra were acquired in healthy mice using both ECG and respiratory-gated, and ungated methods. Z-spectra were also acquired at multiple saturation B1 values to optimize for amide and creatine contrasts. Results: There was no significant difference between CEST contrasts (amide, creatine, MT) calculated from images acquired using ECG and respiratory-gated and ungated methods (p = 0.27, 0.11, 0.47). A saturation power of 1.8$\mu$T provides optimal contrast amplitudes for both amide and total creatine contrast without significantly complicating CEST contrast quantification due to water direct saturation, magnetization transfer, and RF spillover between amide and creatine pools. Further, variability in CEST contrast measurements was significantly reduced using the ungated radial FLASH acquisition (p = 0.002, 0.006 for amide and creatine respectively). Conclusion: This method enables CEST mapping in the murine myocardium without the need for cardiac or respiratory gating. Quantitative CEST contrasts are consistent with those obtained using gated sequences, and per-contrast variance is significantly reduced. This approach makes preclinical cardiac CEST-MRI easily accessible, even for investigators without prior experience in cardiac imaging. |
