Effects of B1+ Heterogeneity on Spin Echo‐Based Liver Iron Estimates
Background Liver iron concentration (LIC) measured by MRI has become the clinical reference standard for managing iron overload in chronically transfused patients. Transverse relaxivity (R2 or R2*) measurements are converted to LIC units using empirically derived calibration curves. Hypothesis That...
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Published in: | Journal of magnetic resonance imaging Vol. 55; no. 5; pp. 1419 - 1425 |
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Main Authors: | , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Hoboken, USA
John Wiley & Sons, Inc
01-05-2022
Wiley Subscription Services, Inc |
Subjects: | |
Online Access: | Get full text |
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Summary: | Background
Liver iron concentration (LIC) measured by MRI has become the clinical reference standard for managing iron overload in chronically transfused patients. Transverse relaxivity (R2 or R2*) measurements are converted to LIC units using empirically derived calibration curves.
Hypothesis
That flip angle (FA) error due to B1+ spatial heterogeneity causes significant LIC quantitation error. B1+ scale (b1, [FAactual/FAspecified]) variation is a major problem at 3 T which could reduce the accuracy of transverse relaxivity measurements.
Study Type
Prospective.
Population
Forty‐seven subjects with chronic transfusional iron overload undergoing clinically indicated LIC assessment.
Field Strength/Sequence
5 T/3 T dual‐repetition time B1+ mapping sequence
Assessment
We quantified the average/standard deviation b1 in the right and left lobes of the liver from B1+ maps acquired at 1.5 T and 3 T. The impact of b1 variation on spin echo LIC estimates was determined using a Monte Carlo model.
Statistical Tests
Mean, median, and standard deviation in whole liver and right and left lobes; two‐sided t‐test between whole‐liver b1 means.
Results
Average b1 within the liver was 99.3% ± 12.3% at 1.5 T versus 69.6% ± 14.6% at 3 T and was independent of iron burden (P < 0.05). Monte Carlo simulations demonstrated that b1 systematically increased R2 estimates at lower LIC (<~25 mg/g at 1.5 T, <~15 mg/g at 3 T) but flattened or even inverted the R2‐LIC relationship at higher LIC (≥~25 mg/g to 1.5 T, ≥~15 mg/g to 3 T); changes in the R2‐LIC relationship were symmetric with respect to over and under excitation and were similar at 1.5 T and 3 T (for the same R2 value). The R2*‐LIC relationship was independent of b1.
Conclusion
Spin echo R2 measurement of LIC at 3 T is error‐prone without correction for b1 errors. The impact of b1 error on current 1.5 T spin echo‐based techniques for LIC quantification is large enough to introduce measurable intersubject variability but the in vivo effect size needs a dedicated validation study.
Level of Evidence
1.
Technical Efficacy Stage
2. |
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Bibliography: | Contract grant sponsor: National Institute of Diabetes, Digestion and Kidney Diseases of the National Institutes of Health; Contract grant number: 1R01DK097115‐01A1. ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1053-1807 1522-2586 |
DOI: | 10.1002/jmri.27928 |