Quantification of myocardial hemorrhage using T2* cardiovascular magnetic resonance at 1.5T with ex-vivo validation.


Journal

Journal of cardiovascular magnetic resonance : official journal of the Society for Cardiovascular Magnetic Resonance
ISSN: 1532-429X
Titre abrégé: J Cardiovasc Magn Reson
Pays: England
ID NLM: 9815616

Informations de publication

Date de publication:
30 09 2021
Historique:
received: 30 01 2021
accepted: 23 05 2021
entrez: 30 9 2021
pubmed: 1 10 2021
medline: 4 11 2021
Statut: epublish

Résumé

T2* cardiovascular magnetic resonance (CMR) is commonly used in the diagnosis of intramyocardial hemorrhage (IMH). For quantifying IMH with T2* CMR, despite the lack of consensus studies, two different methods [subject-specific T2* (ssT2*) and absolute T2* thresholding (aT2* < 20 ms)] are interchangeably used. We examined whether these approaches yield equivalent information. ST elevation myocardial infarction (STEMI) patients (n = 70) were prospectively recruited for CMR at 4-7 days post revascularization and for 6-month follow up (n = 43). Canines studies were performed for validation purposes, where animals (n = 20) were subject to reperfused myocardial infarction (MI) and those surviving the MI (n = 16) underwent CMR at 7 days and 8 weeks and then euthanized. Both in patients and animals, T2* of IMH and volume of IMH were determined using ssT2* and aT2* < 20 ms. In animals, ex-vivo T2* CMR and mass spectrometry for iron concentration ([Fe] While both approaches showed many similarities, there were also differences. Compared to ssT2*, aT2* < 20 ms showed lower T2* and volume of IMH in patients and animals independent of MI age (all p < 0.005). While T2* determined from both methods were highly correlated against [Fe] Current quantification methods have excellent capacity to identify IMH, albeit the T2*of IMH and volume of IMH based on aT2* < 20 ms are smaller compared to ssT2*. Thus the method used to quantify IMH from T2* CMR may influence the diagnosis for IMH.

Sections du résumé

BACKGROUND
T2* cardiovascular magnetic resonance (CMR) is commonly used in the diagnosis of intramyocardial hemorrhage (IMH). For quantifying IMH with T2* CMR, despite the lack of consensus studies, two different methods [subject-specific T2* (ssT2*) and absolute T2* thresholding (aT2* < 20 ms)] are interchangeably used. We examined whether these approaches yield equivalent information.
METHODS
ST elevation myocardial infarction (STEMI) patients (n = 70) were prospectively recruited for CMR at 4-7 days post revascularization and for 6-month follow up (n = 43). Canines studies were performed for validation purposes, where animals (n = 20) were subject to reperfused myocardial infarction (MI) and those surviving the MI (n = 16) underwent CMR at 7 days and 8 weeks and then euthanized. Both in patients and animals, T2* of IMH and volume of IMH were determined using ssT2* and aT2* < 20 ms. In animals, ex-vivo T2* CMR and mass spectrometry for iron concentration ([Fe]
RESULTS
While both approaches showed many similarities, there were also differences. Compared to ssT2*, aT2* < 20 ms showed lower T2* and volume of IMH in patients and animals independent of MI age (all p < 0.005). While T2* determined from both methods were highly correlated against [Fe]
CONCLUSION
Current quantification methods have excellent capacity to identify IMH, albeit the T2*of IMH and volume of IMH based on aT2* < 20 ms are smaller compared to ssT2*. Thus the method used to quantify IMH from T2* CMR may influence the diagnosis for IMH.

Identifiants

pubmed: 34587984
doi: 10.1186/s12968-021-00779-4
pii: 10.1186/s12968-021-00779-4
pmc: PMC8482734
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

104

Subventions

Organisme : NHLBI NIH HHS
ID : R01 HL133407
Pays : United States
Organisme : NIH HHS
ID : HL133407
Pays : United States
Organisme : NIH HHS
ID : HL136578
Pays : United States

Commentaires et corrections

Type : ErratumIn

Informations de copyright

© 2021. The Author(s).

Références

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Auteurs

Yinyin Chen (Y)

Biomedical Imaging Research Institute, Dept of Biomedical Sciences, Cedars-Sinai Medical Center, Suite 400, 8700 Beverly Blvd, Los Angeles, CA, 90048, USA.
Department of Radiology, Zhongshan Hospital, Fudan University, Shanghai, 200032, China.
Department of Medical Imaging, Shanghai Medical School, Fudan University and Shanghai Institute of Medical Imaging, Shanghai, 200032, China.

Daoyuan Ren (D)

Department of Cardiology, Zhongshan Hospital, Fudan University, Shanghai, China.

Xingmin Guan (X)

Biomedical Imaging Research Institute, Dept of Biomedical Sciences, Cedars-Sinai Medical Center, Suite 400, 8700 Beverly Blvd, Los Angeles, CA, 90048, USA.
Department of Bioengineering, University of California at Los Angeles, Los Angeles, CA, USA.

Hsin-Jung Yang (HJ)

Biomedical Imaging Research Institute, Dept of Biomedical Sciences, Cedars-Sinai Medical Center, Suite 400, 8700 Beverly Blvd, Los Angeles, CA, 90048, USA.

Ting Liu (T)

Biomedical Imaging Research Institute, Dept of Biomedical Sciences, Cedars-Sinai Medical Center, Suite 400, 8700 Beverly Blvd, Los Angeles, CA, 90048, USA.
Department of Radiology, The First Affiliated Hospital of China Medical University, Shenyang, 110001, China.

Richard Tang (R)

Biomedical Imaging Research Institute, Dept of Biomedical Sciences, Cedars-Sinai Medical Center, Suite 400, 8700 Beverly Blvd, Los Angeles, CA, 90048, USA.

Hao Ho (H)

Academia Sinica, Taipei, Taiwan.

Hang Jin (H)

Department of Radiology, Zhongshan Hospital, Fudan University, Shanghai, 200032, China.
Department of Medical Imaging, Shanghai Medical School, Fudan University and Shanghai Institute of Medical Imaging, Shanghai, 200032, China.

Mengsu Zeng (M)

Department of Radiology, Zhongshan Hospital, Fudan University, Shanghai, 200032, China. zengmengsu65@gmail.com.
Department of Medical Imaging, Shanghai Medical School, Fudan University and Shanghai Institute of Medical Imaging, Shanghai, 200032, China. zengmengsu65@gmail.com.

Rohan Dharmakumar (R)

Biomedical Imaging Research Institute, Dept of Biomedical Sciences, Cedars-Sinai Medical Center, Suite 400, 8700 Beverly Blvd, Los Angeles, CA, 90048, USA. Rohan.Dharmakumar@cshs.org.
Department of Bioengineering, University of California at Los Angeles, Los Angeles, CA, USA. Rohan.Dharmakumar@cshs.org.

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