T1 and T2 mapping to detect chronic inflammation in cardiac magnetic resonance imaging in heart failure with reduced ejection fraction.


Journal

ESC heart failure
ISSN: 2055-5822
Titre abrégé: ESC Heart Fail
Pays: England
ID NLM: 101669191

Informations de publication

Date de publication:
10 2020
Historique:
received: 04 02 2020
revised: 20 04 2020
accepted: 23 05 2020
pubmed: 14 8 2020
medline: 22 6 2021
entrez: 14 8 2020
Statut: ppublish

Résumé

The purpose of this retrospective single-centre study was to evaluate the non-invasive detection of endomyocardial biopsy (EMB)-established chronic myocardial inflammation in patients with heart failure with reduced ejection fraction (HFrEF) using T1 and T2 mapping. The study population consisted of 52 retrospectively identified HFrEF patients who underwent EMB and cardiac magnetic resonance imaging at 3 Tesla. EMB was defined according to the position statement of the European Society of Cardiology and served as reference to identify inflammation in all patients. A control group of healthy volunteers with prior cardiac magnetic resonance imaging studies (n = 58) was also identified. Global and segmental T1 and T2 values as well as septal measurements and tissue heterogeneity parameters were calculated. Out of the 52 patients with HFrEF, 33 patients had myocardial inflammation detected by EMB, while 19 patients were EMB negative for inflammation. Mean left ventricular ejection fraction was 31% in both groups (P = 0.97). Global T1 and T2 values in HFrEF patients were significantly higher compared with healthy controls (T1 1275 ± 69 ms vs. 1,175 ± 44 ms, P < 0.001; T2 40.0 ± 3.4 ms vs. 37.9 ± 1.6 ms, P < 0.001). The distribution of T1 and T2 values between patients with and without EMB-proven chronic myocardial inflammation was not statistically different when regarding global (T1 1292 ± 71 ms vs. 1266 ± 67 ms, P = 0.26; T2 40.0 ± 2.6 ms vs. 40.0 ± 3.9 ms, P = 1.0), septal (T1 1299 ± 63 ms vs. 1289 ± 76 ms, P = 0.76; T2 40.1 ± 3.5 ms vs 40.0 ± 6.4 ms, P = 0.49) or maximum segmental values (T1 1414 ± 111 ms vs. 1363 ± 88 ms, P = 0.15; T2 47.3 ± 5.2 ms vs. 48.8 ± 11.8 ms, P = 0.53). Mean absolute deviation of segmental T1 and T2 values and log-transformed pixel-wise standard deviation as parameters of tissue heterogeneity did not reveal statistical significant differences between inflammation-positive and inflammation-negative HFrEF patients (all P > 0.4). Conventionally performed quantitative T1 and T2 mapping values significantly correlated with prevalence of HFrEF but did not discriminate HFrEF patients with or without chronic myocardial inflammation in our cohort. This suggests that EMB is the preferred method to detect chronic myocardial inflammation in HFrEF.

Identifiants

pubmed: 32790159
doi: 10.1002/ehf2.12830
pmc: PMC7524213
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2544-2552

Subventions

Organisme : Bundesministerium für Bildung, Wissenschaft, Forschung und Technologie
ID : BMBF 01EO1503
Pays : International

Informations de copyright

© 2020 The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology.

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Auteurs

Tilman Emrich (T)

Department of Diagnostic and Interventional Radiology, University Medical Center Mainz, Mainz, Germany.
German Center for Cardiovascular Research (DZHK), partner site Rhine-Main, Mainz, Germany.

Felix Hahn (F)

Department of Diagnostic and Interventional Radiology, University Medical Center Mainz, Mainz, Germany.

David Fleischmann (D)

Department of Diagnostic and Interventional Radiology, University Medical Center Mainz, Mainz, Germany.

Moritz C Halfmann (MC)

Department of Diagnostic and Interventional Radiology, University Medical Center Mainz, Mainz, Germany.

Christoph Düber (C)

Department of Diagnostic and Interventional Radiology, University Medical Center Mainz, Mainz, Germany.

Akos Varga-Szemes (A)

Department of Radiology and Radiological Science, Medical University of South Carolina, Charleston, SC, USA.

Felicitas Escher (F)

IKDT Institut Kardiale Diagnostik und Therapie GmbH, Berlin, Germany.
Department of Cardiology, Campus Virchow-Klinikum, Charité-University Medicine Berlin, Berlin, Germany.

Evgenia Pefani (E)

Center for Cardiology, Cardiology 1, University Medical Center Mainz, Mainz, Germany.

Thomas Münzel (T)

German Center for Cardiovascular Research (DZHK), partner site Rhine-Main, Mainz, Germany.
Center for Cardiology, Cardiology 1, University Medical Center Mainz, Mainz, Germany.

Heinz-Peter Schultheiss (HP)

IKDT Institut Kardiale Diagnostik und Therapie GmbH, Berlin, Germany.

Karl-Friedrich Kreitner (KF)

Department of Diagnostic and Interventional Radiology, University Medical Center Mainz, Mainz, Germany.

Philip Wenzel (P)

German Center for Cardiovascular Research (DZHK), partner site Rhine-Main, Mainz, Germany.
Center for Cardiology, Cardiology 1, University Medical Center Mainz, Mainz, Germany.
Center for Thrombosis and Hemostasis, University Medical Center Mainz, Mainz, Germany.

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