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ORIGINAL RESEARCH article
Front. Cardiovasc. Med.
Sec. Cardiovascular Imaging
Volume 12 - 2025 | doi: 10.3389/fcvm.2025.1547161
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Background/ Objectives Myocardial and liver iron overload can be assessed through T2* in magnetic resonance imaging (MRI). It is unclear, how T2* measurements are associated with systolic and diastolic left ventricular function assessed by novel feature tracking (FT) strain. Methods Consecutive patients with suspected iron overload undergoing MRI T2* were retrospectively included. T2* was studied continuously and in categories: normal myocardial iron status (T2*≥20ms), myocardial iron overload (T2*<20ms), normal liver iron status (T2* ≥15.4ms) and liver iron overload (T2*<15.4ms). Multivariable regression models were used to assess associations between T2* and FT strain.Results Among 172 participants, longitudinal e/a ratio (-0.17 (-0.27, -0.08), p=0.001), longitudinal early diastolic strain rate (-0.13 (-0.23, -0.03), p=0.014), circumferential late diastolic strain rate (0.18 (0.03, 0.32), p=0.016), longitudinal late diastolic strain rate (0.20 (0.03, 0.36), p=0.019) were associated with higher T2*. Liver iron overload was associated with circumferential systolic strain rate (β=-0.42 (-0.74, -0.09), p=0.014) and longitudinal early diastolic strain rate (0.27 (0.04, 0.49), p=0.023). Combined liver and myocardial iron overload were associated with longitudinal e/a ratio (0.72 (0.19, 1.24), p=0.008). No associations of T2* values with systolic function were found.Conclusion Liver and a combination of myocardial and liver iron overload were associated with increased early diastolic filling and increased e/a ratio respectively, which may serve as markers of diastolic dysfunction. Impaired diastolic function, even in the absence of myocardial iron overload was associated with liver iron metabolism and may indicate early cardiac involvement, while left ventricular systolic function is still preserved.
Keywords: T2*, Iron Overload, Retrospective Studies, feature tracking, Strain, Diastolic function
Received: 17 Dec 2024; Accepted: 05 Mar 2025.
Copyright: © 2025 Quezada-Pinedo, Bernhard, Zurkirchen, Stark, Ahanchi, Gebhard, Ott, Peters, von Tengg-Kobligk, Schütze, Bakula, Wahl, Cajachagua-Torres, Muka and Gräni. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
* Correspondence:
Christoph Gräni, Universitätsklinik für Kardiologie, Schweizer Herz- und Gefässzentrum Bern Inselspital, Universitätsspital Bern, Bern, Switzerland
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