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Updated: May 21, 2026

Fat-Water Phantoms for Magnetic Resonance Imaging Validation: A Flexible and Scalable Protocol
Published on: September 7, 2018
Cross-Vendor Validation of Proton Density Fat Fraction and T1 Mapping Using a Combined Proton Density Fat Fraction-T1
Jitka Starekova1, Sebastian Weingärtner2, David R Rutkowski3
1Department of Radiology, University of Wisconsin-Madison, Madison, Wisconsin, USA.
Proton density fat fraction (PDFF) mapping shows excellent reproducibility in chronic liver disease assessment. However, T1 mapping reproducibility declines with increased fat and T1 values, highlighting the need for fat-corrected T1 mapping.
Area of Science:
- Medical Imaging
- Biomarker Discovery
- Liver Disease Research
Background:
- Chronic liver disease involves coexisting fat and fibroinflammatory changes.
- Biomarkers proton density fat fraction (PDFF) and T1 are typically assessed separately.
- Reproducibility of these biomarkers under mutual confounding is not well understood.
Purpose of the Study:
- To evaluate the multicenter, multi-vendor reproducibility of chemical shift-encoded (CSE)-MRI-based PDFF mapping.
- To assess the reproducibility of MOLLI-based T1 mapping.
- To investigate reproducibility using a combined PDFF-T1 phantom accounting for confounding factors.
Main Methods:
- A prospective phantom study utilizing a commercial PDFF-T1 phantom with varying fat (0%-30%) and T1 (200-1400 ms) values.
- Acquisition of PDFF and T1 maps across four centers and vendors using 1.5T and 3T scanners with specific MRI sequences (SGRE for PDFF, MOLLI for T1).
- Quantitative analysis of maps with assessment of phantom temporal stability over 9 months using intraclass correlation coefficients (ICC) and reproducibility coefficients (RDC).
Main Results:
- PDFF mapping demonstrated excellent overall reproducibility (ICC=0.987, RDC=3.7%), with slight variability increase at higher T1 values.
- T1 mapping showed good reproducibility without fat (RDC 16-161 ms) but moderate to poor reproducibility with increasing fat content (RDC up to 1553 ms at 30% PDFF).
- Excellent temporal stability was observed for both PDFF and T1 mapping over 9 months.
Conclusions:
- This study confirms high reproducibility of PDFF mapping in liver disease assessment.
- T1 mapping reproducibility is significantly affected by fat and T1 levels.
- Fat-corrected T1 mapping is essential for reliable assessment of fibroinflammatory changes in chronic liver disease.
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