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The protons in unsubstituted alkanes are strongly shielded with chemical shifts below 1.8 ppm. Methine, methylene, and methyl protons appear at approximately 1.7, 1.2 and 0.7 ppm, while the proton signal from methane appears at 0.23 ppm. An electronegative substituent, such as chlorine, withdraws the electron density from the protons, increasing their chemical shift. Progressive substitution of the hydrogens in methane by chlorine shifts the proton signals increasingly downfield, to 3.05 ppm in...
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Spin systems where the difference in chemical shifts of the coupled nuclei is greater than ten times J are called first-order spin systems. These nuclei are weakly coupled, and their chemical shifts and coupling constant can generally be estimated from the well-separated signals in the spectrum.
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Chemical shift encoding based double bonds quantification in triglycerides using deep image prior.

Chaoxing Huang1,2, Ziqiang Yu1,2, Zijian Gao1,2

  • 1Department of Imaging and Interventional Radiology, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong, China.

Quantitative Imaging in Medicine and Surgery
|January 22, 2025
PubMed
Summary
This summary is machine-generated.

This study introduces a deep learning method to quantify fatty acid double bonds using MRI, aiding metabolic disorder assessment. The approach, Deep Image Prior (DIP), requires no network training and shows high accuracy in phantom and in-vivo studies.

Keywords:
Deep learningmagnetic resonance imaging (MRI)number of double bonds (ndb)triglyceride

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Area of Science:

  • Biomedical Imaging
  • Artificial Intelligence in Medicine
  • Biochemistry

Background:

  • Fatty acids are crucial biomarkers for metabolic disorders and inflammation.
  • Quantifying double bonds in fatty acids is essential for understanding their role.
  • Current methods for fatty acid analysis can be complex and time-consuming.

Purpose of the Study:

  • To assess a deep learning approach, Deep Image Prior (DIP), for quantifying double bonds and methylene-interrupted double bonds in triglycerides.
  • To evaluate the efficacy of DIP using chemical-shift encoded multi-echo gradient echo images without requiring network training.
  • To validate the method's performance through phantom experiments and in-vivo scans.

Main Methods:

  • Implemented a Deep Image Prior (DIP) model for image reconstruction and parameter refinement.
  • Utilized a cost function based on signal constraints for iterative optimization on single image slices.
  • Performed validation using water-oil phantoms and in-vivo subcutaneous fat imaging.

Main Results:

  • Achieved high concordance between quantified values and reference standards, with a Pearson correlation coefficient of 0.96 in phantom experiments.
  • Demonstrated reliable quantification even with low-fat signals in water-oil phantoms.
  • Showcased consistent in-vivo quantification results comparable to established findings for subcutaneous fat.

Conclusions:

  • Deep Image Prior (DIP) effectively quantifies double bonds and methylene-interrupted double bonds from MRI data.
  • The method offers a promising, training-free approach for fatty acid analysis.
  • Potential for future research and clinical applications in metabolic and inflammatory disease assessment.