Creatine mapping of the brain at 3T by CEST MRI
Kexin Wang1,2, Jianpan Huang3, Licheng Ju1,4
1F.M. Kirby Research Center for Functional Brain Imaging, Kennedy Krieger Research Institute, Baltimore, Maryland, USA.
This study demonstrates that creatine (Cr) mapping in the brain is feasible at 3T using guanidino (Guan) proton resonance. This technique shows potential for detecting intracellular pH and Cr concentration.
Area of Science:
- Neuroimaging
- Biochemistry
- Magnetic Resonance Imaging
Background:
- Creatine (Cr) plays a vital role in cellular energy homeostasis.
- Accurate mapping of brain Cr concentrations is crucial for understanding neurological conditions.
- Current methods for Cr quantification in vivo have limitations.
Purpose of the Study:
- To evaluate the feasibility of creatine (Cr) mapping in the brain at 3 Tesla (3T) using guanidino (Guan) proton resonance.
- To investigate the contributions of Cr and proteins to the GuanCEST signal.
- To assess the potential of GuanCEST for intracellular pH mapping.
Main Methods:
- Utilized wild type and knockout mice with altered Cr concentrations.
- Applied two-step Bloch-McConnell fitting to quantify the Cr proton exchange rate.
- Simulated the pH response of GuanCEST to assess its pH mapping capabilities.
Main Results:
- A distinct Guan proton peak at 2.0 ppm was observed in mouse brains at 3T.
- The creatine chemical exchange saturation transfer (CrCEST) signal contributed approximately 23% to the total GuanCEST signal.
- An estimated exchange rate of 200-300 s⁻¹ was determined for Cr Guan protons.
- Simulations indicated GuanCEST's sensitivity to intracellular pH changes, particularly at lower B₁ field strengths.
Conclusions:
- Creatine chemical exchange saturation transfer (CrCEST) mapping is achievable at 3T.
- This technique holds promise for non-invasively detecting both intracellular pH and Cr concentration in the brain.
- Further research can explore its clinical applications in neurological disorders.
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