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CMR Tissue Characterization in Patients with HFmrEF

Authors :
Moritz Blum
Burkert Pieske
Christian Stehning
Laura Astrid Motzkus
Djawid Hashemi
Hans-Dirk Düngen
Frank Edelmann
Sebastian Kelle
Aleksandar Dordevic
Tomas Lapinskas
Radu Tanacli
Seyedeh Mahsa Zamani
Patrick Doeblin
Elvis Tahirovic
Rolf Gebker
Robin Kraft
Source :
Journal of Clinical Medicine, Vol 8, Iss 11, p 1877 (2019), Journal of Clinical Medicine, Volume 8, Issue 11, Journal of Clinical Medicine, Basel : MDPI, 2019, vol. 8, no. 11, p. 1-12
Publication Year :
2019
Publisher :
MDPI AG, 2019.

Abstract

The characteristics and optimal management of heart failure with a moderately reduced ejection fraction (HFmrEF, LV-EF 40&ndash<br />50%) are still unclear. Advanced cardiac MRI offers information about function, fibrosis and inflammation of the myocardium, and might help to characterize HFmrEF in terms of adverse cardiac remodeling. We, therefore, examined 17 patients with HFpEF, 18 with HFmrEF, 17 with HFrEF and 17 healthy, age-matched controls with cardiac MRI (Phillips 1.5 T). T1 and T2 relaxation time mapping was performed and the extracellular volume (ECV) was calculated. Global circumferential (GCS) and longitudinal strain (GLS) were derived from cine images. GLS (&minus<br />15.7 &plusmn<br />2.1) and GCS (&minus<br />19.9 &plusmn<br />4.1) were moderately reduced in HFmrEF, resembling systolic dysfunction. Native T1 relaxation times were elevated in HFmrEF (1027 &plusmn<br />40 ms) and HFrEF (1033 &plusmn<br />54 ms) compared to healthy controls (972 &plusmn<br />31 ms) and HFpEF (985 &plusmn<br />32 ms). T2 relaxation times were elevated in HFmrEF (55.4 &plusmn<br />3.4 ms) and HFrEF (56.0 &plusmn<br />6.0 ms) compared to healthy controls (50.6 &plusmn<br />2.1 ms). Differences in ECV did not reach statistical significance. HFmrEF differs from healthy controls and shares similarities with HFrEF in cardiac MRI parameters of fibrosis and inflammation.

Details

ISSN :
20770383
Volume :
8
Database :
OpenAIRE
Journal :
Journal of Clinical Medicine
Accession number :
edsair.doi.dedup.....a217f0174261a4464bddbd072abff63d