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  • Open Access

3D coronary dark-blood interleaved with gray-blood (cDIG) MRI

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Journal of Cardiovascular Magnetic Resonance201416 (Suppl 1) :P217

  • Published:


  • Coronary Plaque
  • Calcify Plaque
  • Receiver Bandwidth
  • SSFP Sequence
  • Coronary Vessel Wall


3D dark-blood MRI techniques have shown great potential in coronary plaque burden assessment [1]. However, a substantial variability in quantification could result from superficial calcification that often mimics part of lumen because of low signal. Recent work showed that gray-blood contrast can help to separate superficial calcification from lumen [2]. Thus, the purpose of this study was to develop a 3D coronary dark-blood interleaved with gray-blood (cDIG) MRI technique that potentially improve the visualization and quantification of coronary plaque.

Methods sequence design

The cDIG method is developed based on a balanced SSFP sequence combined with a local reinversion (LocReInv) preparation as proposed by Botnar et al [3]. As with the LocReInv protocol, double inversion pulses are applied every two heartbeats and dark-blood images are collected in the first heartbeat. The novelty of cDIG is the acquisition of gray-blood images by utilizing the second heartbeat during which blood magnetizations have partially recovered. To improve gating efficiency, two independent respiratory navigators are used in two successive heartbeats, for dark-blood and grey-blood imaging, respectively.


The IRB approved study scanned 8 healthy volunteers (age 29 ± 9) on a 3T MR scanner (MAGNETOM Verio, Siemens, Germany). Imaging parameters included: TE/TR = 1.67/3.9 ms, Flip angle = 70, 0.81 × 0.81 mm 2 in-plane resolution (interpolated to 0.41 mm); 2.0 mm slice thickness for 3D cross-sectional imaging and it was interpolated to 1.0 mm for 3D in-plane imaging; 7/8 partial Fourier in phase direction; 822 Hz/pixel receiver bandwidth; 11~25 segments/heartbeat; SPAIR with a delay time of 180 ms for fat suppression. Cross-sectional imaging using LocReInv with the same scan parameters was performed for both image quality and signal intensity comparison. Wilcoxon signed rank test was conducted with p < 0.05 considered as significant.


All scans were successfully completed when using the cDIG and single-contrast LocReInv methods. Representative images are shown in Figure 1. Both vessel wall and lumen are clearly seen in dark-blood images. The values of SNR, CNR, wall thickness, lumen area as well as scan time are not statistically different between cDIG and LocReInv methods (Table 1). The cDIG method provides more information (gray-blood images), potentially facilitating the identification of calcified plaques and thus improving the accuracy of plaque burden assessment.
Figure 1
Figure 1

Representative images of right coronary artery using the cDIG and LocReInv methods.

Table 1

Quantitative analysis results for image quality comparison between cDIG and LocReInv methods


Vessel wall




Epicardial fat








Wall thickness(mm)

Lumen area(mm2)


Time (min)

cDIG (mean ± std)

19.4 ± 4.9

6.6 ± 3.0

9.6 ± 2.1

21.7 ± 6.6

12.8 ± 6.5

9.8 ± 3.8

1.4 ± 0.2

5.4 ± 1.6

8.1 ± 3.4

LocReInv (mean ± std)

20.2 ± 4.4

6.9 ± 2.8

10.8 ± 2.4

25.1 ± 8.2

13.3 ± 5.9

9.4 ± 2.9

1.4 ± 0.1

5.3 ± 1.9

7.0 ± 1.9

Wilcoxon test










Note: ns - not significant


A novel method for simultaneously obtaining coronary vessel wall and gray lumen images was proposed. In vivo experiments show dual contrasts were simultaneously acquired using the proposed method without compromising dark-blood contrast and scan time. This warrants further evaluation of cDIG on more volunteers and patients with coronary atherosclerosis.


NHLBI HL38698, NIBIB EB002623, AHA-11POST7650043.

Authors’ Affiliations

Shenzhen Key Lab for MRI, Shenzhen Institutes of Advanced Technology, Shenzhen, Guangdong, China
Biomedical Imaging Research Institute, Cedars Sinai Medical Center, Los Angeles, California, USA
Union Hospital, Fujian Medical University, Fuzhou, Fujian, China
Siemens Healthcare, Los Angeles, California, USA
Xuanwu Hospital, Capital Medical University, Beijing, China


  1. Kim WY: Circulation. 2007, 115: 228-235.View ArticlePubMedGoogle Scholar
  2. Koktzoglou I: MRM. 2013, 75 (1): 75-85.View ArticleGoogle Scholar
  3. Botnar RM: MRM. 2001, 46 (5): 848-854. 10.1002/mrm.1268.View ArticlePubMedGoogle Scholar


© Xie et al.; licensee BioMed Central Ltd. 2014

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated.