Free-running 4D whole-heart self-navigated golden angle MRI: Initial results
Purpose To test the hypothesis that both coronary anatomy and ventricular function can be assessed simultaneously using a single four‐dimensional (4D) acquisition. Methods A free‐running 4D whole‐heart self‐navigated acquisition incorporating a golden angle radial trajectory was implemented and test...
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Published in | Magnetic resonance in medicine Vol. 74; no. 5; pp. 1306 - 1316 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Blackwell Publishing Ltd
01.11.2015
Wiley Subscription Services, Inc |
Subjects | |
Online Access | Get full text |
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Summary: | Purpose
To test the hypothesis that both coronary anatomy and ventricular function can be assessed simultaneously using a single four‐dimensional (4D) acquisition.
Methods
A free‐running 4D whole‐heart self‐navigated acquisition incorporating a golden angle radial trajectory was implemented and tested in vivo in nine healthy adult human subjects. Coronary magnetic resonance angiography (MRA) datasets with retrospective selection of acquisition window width and position were extracted and quantitatively compared with baseline self‐navigated electrocardiography (ECG) ‐triggered coronary MRA. From the 4D datasets, the left‐ventricular end‐systolic, end‐diastolic volumes (ESV & EDV) and ejection fraction (EF) were computed and compared with values obtained from conventional 2D cine images.
Results
The 4D datasets enabled dynamic assessment of the whole heart with isotropic spatial resolution of 1.15 mm3. Coronary artery image quality was very similar to that of the ECG‐triggered baseline scan despite some SNR penalty. A good agreement between 4D and 2D cine imaging was found for EDV, ESV, and EF.
Conclusion
The hypothesis that both coronary anatomy and ventricular function can be assessed simultaneously in vivo has been tested positive. Retrospective and flexible acquisition window selection allows to best visualize each coronary segment at its individual time point of quiescence. Magn Reson Med 74:1306–1316, 2015. © 2014 Wiley Periodicals, Inc. |
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Bibliography: | ark:/67375/WNG-X790RFFJ-M istex:9FC493E538E1C11E6B46886315DD138409051605 ArticleID:MRM25523 Swiss National Science Foundation - No. 320030_143923 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ISSN: | 0740-3194 1522-2594 1522-2594 |
DOI: | 10.1002/mrm.25523 |