R2 prime (R2′) magnetic resonance imaging for post-myocardial infarction intramyocardial haemorrhage quantification

Author:

Rossello Xavier12,Lopez-Ayala Pedro1,Fernández-Jiménez Rodrigo123,Oliver Eduardo12,Galán-Arriola Carlos12,de Molina-Iracheta Antonio1,Agüero Jaume124,López Gonzalo J1,Lobo-Gonzalez Manuel1,Vílchez-Tschischke Jean Paul15,Fuster Valentin13,Sánchez-González Javier6,Ibanez Borja127ORCID

Affiliation:

1. Translational Laboratory for Cardiovascular Imaging and Therapy, Centro Nacional de Investigaciones Cardiovasculares (CNIC), Madrid, Spain

2. Centro de Investigación Biomédica en Red en Enfermedades Cardiovasculares (CIBERCV), Madrid, Spain

3. Cardiology Department, The Zena and Michael A. Wiener Cardiovascular Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA

4. Department of Cardiology, Hospital Universtitari i Politecnic La Fe, Valencia, Spain

5. Department of Cardiology, Complejo Hospitalario Ruber Juan Bravo, Madrid, Spain

6. Philips Healthcare, Madrid, Spain

7. Department of Cardiology, IIS-Fundación Jiménez Díaz Hospital, Madrid, Spain

Abstract

Abstract Aims To assess whether R2* is more accurate than T2* for the detection of intramyocardial haemorrhage (IMH) and to evaluate whether T2′ (or R2′) is less affected by oedema than T2* (R2*), and thus more suitable for the accurate identification of post-myocardial infarction (MI) IMH. Methods and results Reperfused anterior MI was performed in 20 pigs, which were sacrificed at 120 min, 24 h, 4 days, and 7 days. At each time point, cardiac magnetic resonance (CMR) T2- and T2*-mapping scans were recorded, and myocardial tissue samples were collected to quantify IMH and myocardial water content. After normalization by the number of red blood cells in remote tissue, histological IMH increased 5.2-fold, 10.7-fold, and 4.1-fold at Days 1, 4, and 7, respectively. The presence of IMH was correlated more strongly with R2* (r = 0.69; P = 0.013) than with T2* (r = −0.50; P = 0.085). The correlation with IMH was even stronger for R2′ (r = 0.72; P = 0.008). For myocardial oedema, the correlation was stronger for R2* (r = −0.63; P = 0.029) than for R2′ (r = −0.50; P = 0.100). Multivariate linear regressions confirmed that R2* values were significantly explained by both IMH and oedema, whereas R2′ values were mostly explained by histological IMH (P = 0.024) and were little influenced by myocardial oedema (P = 0.262). Conclusion Using CMR mapping with histological validation in a pig model of reperfused MI, R2′more accurately detected IMH and was less influenced by oedema than R2* (and T2*). Further studies are needed to elucidate whether R2′ is also better suited for the characterization of post-MI IMH in the clinical setting.

Funder

Carlos III Institute of Health–Fondo de Investigacion Sanitaria

European Regional Development Fund

Spanish Ministry of Science, Innovation and Universities

MICIU

Comunidad de Madrid

European structural and investment funds

Ministry of Science, Innovation and Universities MICIU the Instituto de Salud Carlos III

Pro CNIC Foundation

Severo Ochoa Center of Excellence

SEC-CNIC CARDIOJOVEN fellowship

European Union Horizon 2020 research and innovation programme

Marie Skłodowska-Curie

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine,Radiology Nuclear Medicine and imaging,General Medicine

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