Improvement of resolution for brain coupled metabolites by optimized 1H MRS at 7 T
Improvement of resolution for brain coupled metabolites by optimized 1H MRS at 7 T
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DOI:
10.1002/nbm.1529
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发表时间:
2010-11-01
影响因子:
2.9
通讯作者:
Maher, Elizabeth A.
中科院分区:
文献类型:
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作者:
Choi, Changho;Dimitrov, Ivan E.;Maher, Elizabeth A.
Resolution enhancement for glutamate (Glu), glutamine (Gin) and glutathione (GSH) in the human brain by TE-optimized point-resolved spectroscopy (PRESS) at 7T is reported Sub-TE dependences of the multiplets of Glu, Gln, GSH, gamma-aminobutyric acid (GABA) and N-acetylaspartate (NAA) at 2 2-2 6 ppm were investigated with density matrix simulations, incorporating three-dimensional volume localization The numerical simulations indicated that the C4 proton multiplets can be completely separated with (TE1, TE2) = (37, 63) ms, as a result of a narrowing of the multiplets and suppression of the NAA 2 5 ppm signal Phantom experiments reproduced the signal yield and lineshape from simulations within experimental errors In vivo tests of optimized PRESS were conducted on the prefrontal cortex of six healthy volunteers In spectral fitting by LCModel, Cramer-Rao lower bounds (CRLBs) of Glu, Gin and GSH were 2 +/- 1, 5 +/- 1 and 6 +/- 2 (mean +/- SD), respectively To evaluate the performance of the optimized PRESS method under identical experimental conditions, stimulated-echo spectra were acquired with (TE, TM) = (14, 37) and (74, 68) ms The CRIB of Glu was similar between PRESS and short-TE stimulated-echo acquisition mode (STEAM), but the CRLBs of Gin and GSH were lower in PRESS than in both STEAM acquisitions Copyright (C) 2010 John Wiley & Sons, Ltd