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Enhanced Quantitative Phosphocreatine MR Imaging of Skeletal Muscle Using a Global-Local Two-Branch Deep Learning Model.

April 10, 2026pubmed logopapers

Authors

Viswanathan M,Yin L,Kurmi Y,Chai S,Jiang X,Huo Y,Xu J,Chen L,Gore JC,Zu Z

Affiliations (8)

  • Vanderbilt University Institute of Imaging Science, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
  • Department of Biomedical Engineering, Vanderbilt University, Nashville, Tennessee, USA.
  • School of Engineering, Vanderbilt University, Nashville, Tennessee, USA.
  • Department of Radiology and Radiological Sciences, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
  • Department of Electrical and Computer Engineering, Vanderbilt University, Nashville, Tennessee, USA.
  • Department of Computer Science, Vanderbilt University, Nashville, Tennessee, USA.
  • Department of Physics and Astronomy, Vanderbilt University, Nashville, Tennessee, USA.
  • Molecular Physiology and Biophysics, Vanderbilt University, Nashville, Tennessee, USA.

Abstract

Phosphocreatine (PCr) is an essential marker of muscle metabolism, and accurate quantification of its (f<sub>s</sub>) and its exchange rate (k<sub>sw</sub>) is essential for diagnosing various muscular and neuromuscular diseases. Although chemical exchange saturation transfer (CEST) MRI can detect the saturation transfer effect from PCr, quantification of the underlying PCr f<sub>s</sub> and k<sub>sw</sub>, particularly at low fields, remains challenging due to significant overlapping confounding effects in tissues when using conventional fitting approaches. Deep learning (DL) presents a promising alternative, yet traditional DL models often struggle to capture subtle PCr-specific variations induced by changes in f<sub>s</sub> or k<sub>sw</sub>. Furthermore, these models are typically trained on either fully synthetic data, which may not adequately mimic tissues, or in vivo data which lack ground truth. This study introduces a global-local two-branch DL model to effectively eliminate confounding effects and capture subtle variations in the PCr CEST effect. Furthermore, our model was trained on partially synthetic data that offers both simulation flexibility and fidelity. Model accuracy was evaluated by using both digital and physical phantoms, and the model was applied to skeletal muscle of healthy rats and rats with amyotrophic lateral sclerosis (ALS). Phantom experiments demonstrate that our approach surpasses all fitting methods, the state-of-the-art model, and other combinations of DL models and training data. In vivo, the model identified a significant reduction in PCr f<sub>s</sub> in ALS rats, which other methods fail to detect. Our global-local two-branch DL model trained using partially synthetic data enhances PCr quantification in skeletal muscle.

Topics

Journal Article

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