Subscribe to RSS
DOI: 10.1055/s-0043-1772467
Diagnostic Value of T1 Mapping in Detecting Iron Overload in Indian Patients with Thalassemia Major: A Comparison with T2* Mapping
Funding None.Abstract
Purpose T2* is the gold standard for iron quantification in liver as well as myocardium. In this study, we evaluated the diagnostic accuracy of myocardial T1 mapping for the assessment of myocardial iron overload (MIO) as compared to the T2* mapping in patients with thalassemia major (TM).
Methods Consecutive TM patients attending the thalassemia clinic were prospectively enrolled. Magnetic resonance imaging was performed on a 1.5 T scanner (Siemens Healthineers, Germany) using a gradient echo T2* as well as a T1 mapping (MOLLI) sequence done at a mid-ventricular short-axis single 8 mm slice of the left ventricle. Values were analyzed by manually drawing a region of interest in the mid-septum. T2*less than 20ms was used as the cutoff for significant MIO.
Results One-hundred three patients (58 males, mean age: 17 ± 7.8 years, mean ferritin: 2009.5 µg/L) underwent cardiovascular magnetic resonance. Median T2* of myocardium was 33.45ms. Nineteen patients (18.4%) had T2*less than 20ms. T1 value was low (<850ms) in all the patients with T2* less than 20 ms. Receiver operating characteristic curve analysis revealed the best cutoff of native T1 mapping value as 850 ms which had high specificity (95.2%), sensitivity (94.2%) and negative predictive value (98.8%) for T2* less than 20ms. There was excellent agreement between T1 and T2* for diagnosis of MIO (Kappa—0.848, p <0.001). We did not find any patient who had normal T1 mapping values but had MIO on T2*.
Conclusion T1 and T2* correlate well and normal T1 values may rule out presence of MIO. T1 mapping can act as additional imaging marker for MIO and may be helpful in centers with nonavailability or limited experience of T2*.
Data Availability
The data used to support the findings of this study are available from the corresponding author upon request.
Ethical Statement
Research involved human participants The work described has been carried out in accordance with The Code of Ethics of the World Medical Association (Declaration of Helsinki) for experiments involving humans.
Ethical Approval
The study was performed according to the Code of Ethics (Declaration of Helsinki).
Informed Consent
Informed consent was obtained from all the participants.
Author Contributions
S.P.S., P.J., and V.O. wrote the manuscript and did statistical analysis. T.S., N.N., K.P.G., and M.V. helped with clinical care of the patients and conceived the study design and critically revised the manuscript for important intellectual content and final approval of the version to be submitted. S.K. helped with the images and revised the manuscript. All authors read and approved the final manuscript.
Publication History
Article published online:
04 September 2023
© 2023. Indian Radiological Association. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)
Thieme Medical and Scientific Publishers Pvt. Ltd.
A-12, 2nd Floor, Sector 2, Noida-201301 UP, India
-
References
- 1 Modell B, Khan M, Darlison M, Westwood MA, Ingram D, Pennell DJ. Improved survival of thalassaemia major in the UK and relation to T2* cardiovascular magnetic resonance. J Cardiovasc Magn Reson 2008; 10 (01) 42
- 2 Marsella M, Borgna-Pignatti C, Meloni A. et al. Cardiac iron and cardiac disease in males and females with transfusion-dependent thalassemia major: a T2* magnetic resonance imaging study. Haematologica 2011; 96 (04) 515-520
- 3 Merchant R, Joshi A, Ahmed J, Krishnan P, Jankharia B. Evaluation of cardiac iron load by cardiac magnetic resonance in thalassemia. Indian Pediatr 2011; 48 (09) 697-701
- 4 Perifanis V, Tziomalos K, Tsatra I, Karyda S, Patsiaoura K, Athanassiou-Metaxa M. Prevalence and severity of liver disease in patients with b thalassemia major. A single-institution fifteen-year experience. Haematologica 2005; 90 (08) 1136-1138
- 5 Puliyel M, Sposto R, Berdoukas VA. et al. Ferritin trends do not predict changes in total body iron in patients with transfusional iron overload. Am J Hematol 2014; 89 (04) 391-394
- 6 Schmitt B, Golub RM, Green R. Screening primary care patients for hereditary hemochromatosis with transferrin saturation and serum ferritin level: systematic review for the American College of Physicians. Ann Intern Med 2005; 143 (07) 522-536
- 7 Wood JC, Glynos T, Thompson A. et al. Relationship between labile plasma iron, liver iron concentration and cardiac response in a deferasirox monotherapy trial. Haematologica 2011; 96 (07) 1055-1058
- 8 Brittenham GM, Griffith PM, Nienhuis AW. et al. Efficacy of deferoxamine in preventing complications of iron overload in patients with thalassemia major. N Engl J Med 1994; 331 (09) 567-573
- 9 Olson LJ, Edwards WD, Holmes Jr DR, Miller Jr FA, Nordstrom LA, Baldus WP. Endomyocardial biopsy in hemochromatosis: clinicopathologic correlates in six cases. J Am Coll Cardiol 1989; 13 (01) 116-120
- 10 Brittenham GM. New advances in iron metabolism, iron deficiency, and iron overload. Curr Opin Hematol 1994; 1 (02) 101-106
- 11 Barosi G, Arbustini E, Gavazzi A, Grasso M, Pucci A. Myocardial iron grading by endomyocardial biopsy. A clinico-pathologic study on iron overloaded patients. Eur J Haematol 1989; 42 (04) 382-388
- 12 Storey P, Thompson AA, Carqueville CL, Wood JC, de Freitas RA, Rigsby CK. R2* imaging of transfusional iron burden at 3T and comparison with 1.5T. J Magn Reson Imaging 2007; 25 (03) 540-547
- 13 Ghugre NR, Coates TD, Nelson MD, Wood JC. Mechanisms of tissue-iron relaxivity: nuclear magnetic resonance studies of human liver biopsy specimens. Magn Reson Med 2005; 54 (05) 1185-1193
- 14 Anderson LJ, Holden S, Davis B. et al. Cardiovascular T2-star (T2*) magnetic resonance for the early diagnosis of myocardial iron overload. Eur Heart J 2001; 22 (23) 2171-2179
- 15 Pepe A, Positano V, Santarelli MF. et al. Multislice multiecho T2* cardiovascular magnetic resonance for detection of the heterogeneous distribution of myocardial iron overload. J Magn Reson Imaging 2006; 23 (05) 662-668
- 16 Karamitsos TD, Francis JM, Myerson S, Selvanayagam JB, Neubauer S. The role of cardiovascular magnetic resonance imaging in heart failure. J Am Coll Cardiol 2009; 54 (15) 1407-1424
- 17 Shaw M, Ojha V, Ganga KP. et al. Reference values of myocardial native T1 and T2 mapping values in normal Indian population at 1.5 Tesla scanner. Int J Cardiovasc Imaging 2022; 38 (11) 2403-2411
- 18 Torlasco C, Cassinerio E, Roghi A. et al. Role of T1 mapping as a complementary tool to T2* for non-invasive cardiac iron overload assessment. PLoS One 2018; 13 (02) e0192890
- 19 Sado DM, Maestrini V, Piechnik SK. et al. Noncontrast myocardial T1 mapping using cardiovascular magnetic resonance for iron overload. J Magn Reson Imaging 2015; 41 (06) 1505-1511
- 20 Krittayaphong R, Zhang S, Saiviroonporn P. et al. Detection of cardiac iron overload with native magnetic resonance T1 and T2 mapping in patients with thalassemia. Int J Cardiol 2017; 248: 421-426
- 21 Meloni A, Martini N, De Luca A. et al. Myocardial native T1 mapping and cardiac outcomes in thalassemia major. Eur Heart J Cardiovasc Imaging 2021;22(Supplement_1; jeaa356.311)