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Updated: Apr 6, 2026

Author Spotlight: A Non-Invasive Tool to Assess and Differentiate Fat Patterns in Liver Using 3D Dixon MRI
Published on: October 20, 2023
Accelerating MR Imaging Liver Steatosis Measurement Using Combined Compressed Sensing and Parallel Imaging: A
Louis W Mann1, David M Higgins1, Carl N Peters1
1From the Newcastle Magnetic Resonance Centre (L.W.M., C.N.P., K.K.H., A.C., R.T., K.G.H.) and MoveLab (S.C.), Institute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, NE4 5PL, England; and Philips Healthcare, Guildford, England (D.M.H.).
Accelerated magnetic resonance imaging (MRI) using compressed sensing and parallel imaging (CS-PI) allows for faster liver fat fraction measurements. This technique is accurate up to 3.8x acceleration, significantly reducing breath-hold times.
Area of Science:
- Magnetic Resonance Imaging
- Medical Imaging Physics
- Quantitative MRI
Background:
- Liver fat fraction quantification is crucial for diagnosing and monitoring non-alcoholic fatty liver disease.
- Conventional MRI methods require long breath-hold periods, limiting patient comfort and increasing motion artifacts.
- Accelerated MRI techniques aim to reduce scan times without compromising diagnostic accuracy.
Purpose of the Study:
- To evaluate the accuracy and reliability of accelerated hepatic fat fraction and R2* relaxation rate measurements.
- To compare accelerated MRI reconstructions with conventional fully sampled acquisitions using Bland-Altman analysis.
- To assess the impact of acceleration factors on image quality and quantitative accuracy.
Main Methods:
- Prospective acquisition of undersampled data at various acceleration ratios (2.6x to 4.8x) alongside fully sampled data.
- Reconstruction of fat fraction maps using combined compressed sensing and parallel imaging (CS-PI).
- Bland-Altman analysis for limits of agreement, inter- and intrarater variability, and image quality assessment.
Main Results:
- Accelerated acquisitions showed high agreement with fully sampled data, with 95% limits of agreement for fat fractions ranging from 1.1% to 1.5%.
- Acceleration up to 3.8x did not significantly degrade fat fraction measurements compared to intra- and interrater variability.
- Image quality remained acceptable up to 3.8x acceleration, with minimal artifacts, while higher acceleration (4.8x) introduced substantial artifacts.
Conclusions:
- Prospective undersampling combined with CS-PI reconstruction effectively accelerates liver fat fraction measurements.
- The technique is reliable and accurate up to a 3.8x acceleration factor.
- This acceleration significantly reduces breath-hold duration from 17.7 to 4.7 seconds, improving clinical feasibility.
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