Liver Iron Content Determination Using a Volumetric Breath‐Hold Gradient‐Echo Sequence With In‐Line R2* Calculation. Issue 5 (7th May 2020)

• Record Type: Journal Article
• Authors: Wunderlich, Arthur P.; Schmidt, Stefan A.; Mauro, Valeria; Kneller, Lena; Kannengießer, Stephan; Beer, Meinrad; Cario, Holger
• Is Part Of: Journal of magnetic resonance imaging. Volume 52:Issue 5(2020)
• Page Start: 1550
• Page End: 1556
• Publication Date: 2020-05-07
• Subjects: magnetic resonance imaging -- iron overload -- hematology -- thalassemia -- anemia; Magnetic resonance imaging -- Periodicals; 616
• DOI: 10.1002/jmri.27185
• Languages: English
• ISSNs: 1053-1807

Abstract

Abstract : 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 (R 2 = 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