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Transthoracic Speckle Tracking Echocardiography for the Quantitative Assessment of Left Ventricular Myocardial Deformation
Published on: October 20, 2016
Myocardial deformation in iron overload cardiomyopathy: speckle tracking imaging in a beta-thalassemia major
Luca Antonio Felice Di Odoardo1, Marianna Giuditta2,3, Elena Cassinerio3
1Cardiovascular Disease Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, University of Milan, via F. Sforza 35, 20122, Milan, Italy. lucadiod@inwind.it.
Insights
Strain imaging detects subclinical myocardial dysfunction in thalassemia major patients, even without significant iron overload. This method aids in timing cardioactive treatments for iron cardiomyopathy.
Area of Science:
- Cardiology
- Medical Imaging
- Hematology
Background:
- Traditional echocardiography fails to detect early iron overload cardiomyopathy and myocardial iron deposition.
- Thalassemia major (TM) patients are at risk for cardiac complications due to iron overload.
Purpose of the Study:
- To determine myocardial systolic strain indices in TM patients.
- To assess the relationship between strain indices and cardiac magnetic resonance (CMR) T2* values, an indicator of myocardial iron overload severity.
Main Methods:
- Speckle tracking analysis was used to assess regional myocardial strains and rotation in 55 TM patients and 20 controls.
- TM patients were categorized into groups based on CMR-T2* values (low T2* ≤20 ms for significant iron overload, normal T2* >20 ms).
Main Results:
- TM patients exhibited significantly decreased circumferential and radial strain and reduced end-systolic rotation compared to controls.
- No significant differences in strain or rotation were found between TM groups with low and normal T2* values.
- No significant correlation was observed between myocardial strain, rotation, and CMR-T2* values.
Conclusions:
- Myocardial iron overload is not the sole cause of iron cardiomyopathy in TM.
- Strain imaging can identify subclinical myocardial dysfunction in TM patients, independent of CMR-T2* values.
- Strain imaging may assist in optimizing the timing of cardioactive treatments for TM patients.
Abstract:
Traditional echocardiography is unable to detect neither the early stages of iron overload cardiomyopathy nor myocardial iron deposition. The aim of the study is to determine myocardial systolic strain indices in thalassemia major (TM), and assess their relationship with T2*, a cardiac magnetic resonance index of the severity of cardiac iron overload. 55 TM cases with recent cardiac magnetic resonance (CMR-T2*) underwent speckle tracking analysis to assess regional myocardial strains and rotation. The results were compared with a normal control group (n = 20), and were subsequently analyzed on the basis of the CMR-T2* values. Two TM groups were studied: TM with significant cardiac iron overload ("low" T2*, ≤20 ms; n = 21), and TM with normal T2* values ("normal" T2*, >20 ms; n = 34). TM patients show significant, uniform decrease in circumferential and radial strain (P < 0.05), and a remarkable reduction in end-systolic rotation, both global, and for all segments (P < 0.001). No significant differences were found between the low- and the normal T2* group either in regional strains and rotation or in standard echocardiographic and CMR parameters. Spearman's correlation coefficient shows no significant correlation between myocardial strains, rotation and cardiac T2* values. In conclusion, our results are in accordance with recent evidence that myocardial iron overload is not the only mechanism underlying iron cardiomyopathy in TM. Strain imaging can predict subclinical myocardial dysfunction irrespective of CMR-T2* values, although it cannot replace CMR-T2* in assessing cardiac iron overload. Finally, it might be useful to appropriately time cardioactive treatment.
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