These two authors contributed equally.
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Research Article
Fast T2 relaxometry with an accelerated multi-echo spin-echo sequence
Article first published online: 31 MAY 2010
DOI: 10.1002/nbm.1521
Copyright © 2010 John Wiley & Sons, Ltd.
Additional Information
How to Cite
Sénégas, J., Liu, W., Dahnke, H., Song, H., Jordan, E. K. and Frank, J. A. (2010), Fast T2 relaxometry with an accelerated multi-echo spin-echo sequence. NMR Biomed., 23: 958–967. doi: 10.1002/nbm.1521
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These two authors contributed equally.
Publication History
- Issue published online: 31 MAY 2010
- Article first published online: 31 MAY 2010
- Manuscript Revised: 19 JAN 2010
- Manuscript Accepted: 19 JAN 2010
- Manuscript Received: 16 JUL 2009
Funded by
- Intramural Research Program at the Clinical Center at the National Institutes of Health
- Cooperative research and development agreement with Philips Research North America
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- Cited By
Keywords:
- T2 relaxometry;
- undersampling;
- k-t BLAST;
- k-t GRAPPA;
- SPIO labeled cells
Abstract
A new method has been developed to reduce the number of phase-encoding steps in a multi-echo spin-echo imaging sequence allowing fast T2 mapping without loss of spatial resolution. In the proposed approach, the k-space data at each echo time were undersampled and a reconstruction algorithm that exploited the temporal correlation of the MR signal in k-space was used to reconstruct alias-free images. A specific application of this algorithm with multiple-receiver acquisition, offering an alternative to existing parallel imaging methods, has also been introduced. The fast T2 mapping method has been validated in human brain T2 measurements in a group of nine volunteers with acceleration factors up to 3.4. The results demonstrated that the proposed method exhibited excellent linear correlation with the regular T2 mapping with full sampling and achieved better image reconstruction and T2 mapping with respect to SNR and reconstruction artifacts than the selected reference acceleration techniques. The new method has also been applied for quantitative tracking of injected magnetically labeled breast cancer cells in the rat brain with acceleration factors of 1.8 and 3.0. The proposed technique can provide an effective approach for accelerated T2 quantification, especially for experiments with single-channel coil when parallel imaging is not applicable. Copyright © 2010 John Wiley & Sons, Ltd.