Effects of B₁⁺ Heterogeneity on Spin Echo-Based Liver Iron Estimates

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.

That flip angle (FA) error due to B₁⁺ spatial heterogeneity causes significant LIC quantitation error. B₁⁺ scale (b₁ , [FA_actual /FA_specified ]) variation is a major problem at 3 T which could reduce the accuracy of transverse relaxivity measurements.

Prospective.

Forty-seven subjects with chronic transfusional iron overload undergoing clinically indicated LIC assessment.

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.

Mean, median, and standard deviation in whole liver and right and left lobes; two-sided t-test between whole-liver b₁ means.

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 .

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.

2.