Background
Liver iron overload is a serious condition occurring in patients requiring blood transfusions (eg, in thalassemia and different forms of anemia) or with dysfunctional iron resorption, since there is no physiological mechanism to excrete iron. Above a certain level of iron concentration, chelation therapy is indicated. To monitor therapy success, liver iron content should be assessed regularly. A noninvasive method is important for patient management. Existing MRI methods suffer from long acquisition times and cost.
Purpose
To study the correlation of liver iron content (LIC) reference values to liver R2* determined using a 3D breath‐hold multigradient echo (GRE) MRI sequence, employing accelerated acquisition by parallel imaging and in‐line R2* calculation.
Study type
Prospective.
Population
In all, 117 patients (22.1 ± 14.1 years, 66 men) suspected of iron overload.
Sequence
GRE.
Field Strength
1.5T.
Assessment
For comparison, a regulatory‐approved method with a considerably longer scan time was used, providing LIC reference values. Participants were divided into a calibration group (65 participants), analyzed independently by two observers, and a validation group (52 participants).
Statistical Tests
Linear correlation parameters were evaluated for R2* values with LIC reference values, and for LIC determined from R2* for validation group participants with LIC reference values. Sensitivity/specificity for clinical relevant LIC thresholds were analyzed. Interobserver variability was determined by intraclass correlation coefficient (ICC).
Results
Interobserver agreement was excellent, with an ICC of 0.99, P < 0.001. Good correlation (R2 = 0.89) and congruence of LIC values obtained with our method to LIC reference values was found, and almost identical diagnostic accuracy. Sensitivity/specificity were 0.98/0.67 for the diagnostic relevant LIC threshold of 4.5 mg/g and 1.0/0.95 for the threshold of 7 mg/g.
Data Conclusion
MRI acquisition times for determination of LIC can be significantly reduced by the use of comprehensive in‐line R2* map generation without compromising diagnostic accuracy.
Level of Evidence
1
Technical Efficacy Stage
2