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Improving accuracy of myocardial T estimation in MyoMapNet. | LitMetric

AI Article Synopsis

  • The study aims to enhance T estimation accuracy using MyoMapNet, a deep learning model that employs four T-weighted images in cardiac T mapping.
  • MyoMapNet was retrained with numerical simulations and phantom MRI data, leading to improved performance, as demonstrated when tested against new phantom vials.
  • Results indicated that MyoMapNet provided T values highly correlated with standard references and showed robustness against variable imaging conditions, suggesting it is a reliable tool for measuring myocardial T values.

Article Abstract

Purpose: To improve the accuracy and robustness of T estimation by MyoMapNet, a deep learning-based approach using 4 inversion-recovery T -weighted images for cardiac T mapping.

Methods: MyoMapNet is a fully connected neural network for T estimation of an accelerated cardiac T mapping sequence, which collects 4 T -weighted images by a single Look-Locker inversion-recovery experiment (LL4). MyoMapNet was originally trained using in vivo data from the modified Look-Locker inversion recovery sequence, which resulted in significant bias and sensitivity to various confounders. This study sought to train MyoMapNet using signals generated from numerical simulations and phantom MR data under multiple simulated confounders. The trained model was then evaluated by phantom data scanned using new phantom vials that differed from those used for training. The performance of the new model was compared with modified Look-Locker inversion recovery sequence and saturation-recovery single-shot acquisition for measuring native and postcontrast T in 25 subjects.

Results: In the phantom study, T values measured by LL4 with MyoMapNet were highly correlated with reference values from the spin-echo sequence. Furthermore, the estimated T had excellent robustness to changes in flip angle and off-resonance. Native and postcontrast myocardium T at 3 Tesla measured by saturation-recovery single-shot acquisition, modified Look-Locker inversion recovery sequence, and MyoMapNet were 1483 ± 46.6 ms and 791 ± 45.8 ms, 1169 ± 49.0 ms and 612 ± 36.0 ms, and 1443 ± 57.5 ms and 700 ± 57.5 ms, respectively. The corresponding extracellular volumes were 22.90% ± 3.20%, 28.88% ± 3.48%, and 30.65% ± 3.60%, respectively.

Conclusion: Training MyoMapNet with numerical simulations and phantom data will improve the estimation of myocardial T values and increase its robustness to confounders while also reducing the overall T mapping estimation time to only 4 heartbeats.

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Source
http://dx.doi.org/10.1002/mrm.29397DOI Listing

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