A Novel CEST-Based Approach for Reliably Assessing Skeletal Muscle Oxidative Phosphorylation: OXCEST
Ritambhar Burman1, Yuxi Pang1, Asim Bag1
1Department of Radiology, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
Magnetic Resonance in Medicine
|October 23, 2025
Summary
This study introduces OXCEST, a novel MRI method for mapping skeletal muscle oxidative phosphorylation. OXCEST reliably assesses creatine recovery post-exercise, correlating well with established 31P-MRS methods.
Area of Science:
- Biomedical Engineering
- Magnetic Resonance Imaging
- Metabolic Imaging
Background:
- Skeletal muscle oxidative phosphorylation (OXPHOS) is crucial for energy metabolism.
- Accurate assessment of OXPHOS is vital for understanding muscle function and disease.
- Current methods for measuring OXPHOS have limitations in accessibility and resolution.
Purpose of the Study:
- To develop and validate a novel Chemical Exchange Saturation Transfer (CEST) MRI method, termed OXCEST, for mapping skeletal muscle OXPHOS.
- To assess the reliability and accuracy of the OXCEST method in quantifying creatine (Cr) recovery post-exercise.
Main Methods:
- The OXCEST method utilizes two frequency offsets to acquire creatine-weighted CEST maps.
- It models pre-exercise MTRasym as a function of B0 to account for field inhomogeneity.
- Post-exercise changes in MTRasym are analyzed to quantify Cr-related recovery, validated against 31P-MRS.
Main Results:
- The B0 correction function demonstrated high reliability across different muscle groups (R2 > 0.87).
- OXCEST successfully captured exercise-induced increases in MTRasym, showing mono-exponential recovery.
- OXCEST-derived creatine recovery time constant (TCr) showed significant correlation (R2 = 0.83) with 31P-MRS TPCr.
Conclusions:
- OXCEST provides a reliable method for assessing post-exercise creatine recovery in skeletal muscle.
- The developed OXCEST technique shows good agreement with the gold standard 31P-MRS.
- This novel MRI method holds promise for non-invasive evaluation of muscle metabolic function.


