T1 Mapping in Cardiovascular Magnetic Resonance—A Marker of Diffuse Myocardial Fibrosis in Patients Undergoing Hematopoietic Stem Cell Transplantation

Author:

Vaitiekiene Audrone1,Kulboke Migle23,Bieseviciene Monika1,Jankauskas Antanas45,Bartnykaite Agne6ORCID,Rinkuniene Diana7,Strazdiene Igne1,Lidziute Emilija8,Jankauskaite Darija8,Gaidamavicius Ignas23,Bucius Paulius1,Lapinskas Tomas1,Gerbutavicius Rolandas23,Juozaityte Elona23ORCID,Vaskelyte Jolanta Justina15,Vaitiekus Domas23ORCID,Sakalyte Gintare15

Affiliation:

1. Department of Cardiology, Medical Academy, Lithuanian University of Health Sciences, 44307 Kaunas, Lithuania

2. Department of Oncology and Hematology, Medical Academy, Lithuanian University of Health Sciences, 44307 Kaunas, Lithuania

3. Oncology Institute, Lithuanian University of Health Sciences, 50161 Kaunas, Lithuania

4. Department of Radiology, Medical Academy, Lithuanian University of Health Sciences, 44307 Kaunas, Lithuania

5. Institute of Cardiology, Lithuanian University of Health Sciences, 44307 Kaunas, Lithuania

6. Oncology Research Laboratory, Oncology Institute, Lithuanian University of Health Sciences, 50161 Kaunas, Lithuania

7. Institute of Physiology and Pharmacology, Medical Academy, Lithuanian University of Health Sciences, 44307 Kaunas, Lithuania

8. Medical Academy, Lithuanian University of Health Sciences, 44307 Kaunas, Lithuania

Abstract

Introduction: Hematopoietic stem cell transplantation (HSCT) recipients are at increased risk of cardiovascular diseases. In our study, we aimed to find subclinical changes in myocardial tissue after HSCT with the help of cardiovascular magnetic resonance (CMR) tissue imaging techniques. Methods: The data of 44 patients undergoing autologous and allogeneic HSCT in the Hospital of Lithuanian University of Health Sciences Kaunas Clinics from October 2021 to February 2023 were analyzed. Bioethics approval for the prospective study was obtained (No BE-2-96). CMR was performed two times: before enrolling for the HSCT procedure (before starting mobilization chemotherapy for autologous HSCT and before starting the conditioning regimen for allogeneic HSCT) and 12 ± 1 months after HSCT. LV end-diastolic volume, LV end-systolic volume, LV mass and values indexed to body surface area (BSA), and LV ejection fraction were calculated. T1 and T2 mapping values were measured. Results: There was a statistically significant change in T1 mapping values. Before HSCT, mean T1 mapping was 1226.13 ± 39.74 ms, and after HSCT, it was 1248.70 ± 41.07 ms (p = 0.01). The other parameters did not differ significantly. Conclusions: Increases in T1 mapping values following HSCT can show the progress of diffuse myocardial fibrosis and may reflect subclinical injury. T2 mapping values remain the same and do not show edema and active inflammation processes at 12 months after HSCT.

Publisher

MDPI AG

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