Volume 81, Issue 1 pp. 153-166
FULL PAPER

Black blood myocardial T2 mapping

Chengyan Wang

Chengyan Wang

Department of Medicine (Cardiovascular Division), Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts

Academy for Advanced Interdisciplinary Studies, Peking University, Beijing, People's Republic of China

Chengyan Wang and Jihye Jang contributed equally to this study.

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Jihye Jang

Jihye Jang

Department of Medicine (Cardiovascular Division), Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts

Department of Computer Science, Technical University of Munich, Munich, Germany

Chengyan Wang and Jihye Jang contributed equally to this study.

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Ulf Neisius

Ulf Neisius

Department of Medicine (Cardiovascular Division), Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts

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Maryam Nezafat

Maryam Nezafat

Department of Medicine (Cardiovascular Division), Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts

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Ahmed Fahmy

Ahmed Fahmy

Department of Medicine (Cardiovascular Division), Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts

Biomedical Engineering Department, Cairo University, Giza, Egypt

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Jinkyu Kang

Jinkyu Kang

Department of Medicine (Cardiovascular Division), Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts

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Jennifer Rodriguez

Jennifer Rodriguez

Department of Medicine (Cardiovascular Division), Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts

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Beth Goddu

Beth Goddu

Department of Medicine (Cardiovascular Division), Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts

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Patrick Pierce

Patrick Pierce

Department of Medicine (Cardiovascular Division), Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts

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Sophie Berg

Sophie Berg

Department of Medicine (Cardiovascular Division), Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts

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Jue Zhang

Jue Zhang

Academy for Advanced Interdisciplinary Studies, Peking University, Beijing, People's Republic of China

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Xiaoying Wang

Xiaoying Wang

Academy for Advanced Interdisciplinary Studies, Peking University, Beijing, People's Republic of China

Department of Radiology, Peking University First Hospital, Beijing, People's Republic of China

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Reza Nezafat

Corresponding Author

Reza Nezafat

Department of Medicine (Cardiovascular Division), Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts

Correspondence

Reza Nezafat, Beth Israel Deaconess Medical Center, 330 Brookline Ave, Boston, MA, 02215.

Email: [email protected]

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First published: 29 July 2018
Citations: 19

Funding information: This study is supported in part by the National Institutes of Health (NIH) 1R01HL129185-01, 1R21HL127650, and 1R01HL129157; and the American Heart Association (AHA) 15EIA22710040. Chengyan Wang is funded by the National Science Foundation of China 81627901, and 81571666; and the China Postdoctoral Science Foundation 17Z102060138

Abstract

Purpose

To develop a black blood heart-rate adaptive T2-prepared balanced steady-state free-precession (BEATS) sequence for myocardial T2 mapping.

Methods

In BEATS, blood suppression is achieved by using a combination of preexcitation and double inversion recovery pulses. The timing and flip angles of the preexcitation pulse are auto-calculated in each patient based on heart rate. Numerical simulations, phantom studies, and in vivo studies were conducted to evaluate the performance of BEATS. BEATS T2 maps were acquired in 36 patients referred for clinical cardiac MRI and in 1 swine with recent myocardial infarction. Two readers assessed all images acquired in patients to identify the presence of artifacts associated with slow blood flow.

Results

Phantom experiments showed that the BEATS sequence provided accurate T2 values over a wide range of simulated heart rates. Black blood myocardial T2 maps were successfully obtained in all subjects. No significant difference was found between the average T2 measurements obtained from the BEATS and conventional bright-blood T2; however, there was a decrease in precision using the BEATS sequence. A suppression of the blood pool resulted in sharper definition of the blood–myocardium border and reduced partial voluming effect. The subjective assessment showed that 16% (18 out of 108) of short-axis slices have residual blood artifacts (12 in the apical slice, 4 in the midventricular slice, and 2 in the basal slice).

Conclusion

The BEATS sequence yields dark blood myocardial T2 maps with better definition of the blood–myocardium border. Further studies are warranted to evaluate diagnostic accuracy of black blood T2 mapping.

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