Metabolite-cycled density-weighted concentric rings k-space trajectory (DW-CRT) enables high-resolution 1 H magnetic resonance spectroscopic imaging at 3-Tesla.
Metabolite-cycled density-weighted concentric rings k-space trajectory (DW-CRT) enables high-resolution 1 H magnetic resonance spectroscopic imaging at 3-Tesla.
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DOI:
10.1038/s41598-018-26096-y
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发表时间:
2018-05-17
影响因子:
4.6
通讯作者:
Emir UE
中科院分区:
文献类型:
--
作者:
Steel A;Chiew M;Jezzard P;Voets NL;Plaha P;Thomas MA;Stagg CJ;Emir UE
Magnetic resonance spectroscopic imaging (MRSI) is a promising technique in both experimental and clinical settings. However, to date, MRSI has been hampered by prohibitively long acquisition times and artifacts caused by subject motion and hardware-related frequency drift. In the present study, we demonstrate that density weighted concentric ring trajectory (DW-CRT) k-space sampling in combination with semi-LASER excitation and metabolite-cycling enables high-resolution MRSI data to be rapidly acquired at 3 Tesla. Single-slice full-intensity MRSI data (short echo time (TE) semi-LASER TE = 32 ms) were acquired from 6 healthy volunteers with an in-plane resolution of 5 × 5 mm in 13 min 30 sec using this approach. Using LCModel analysis, we found that the acquired spectra allowed for the mapping of total N-acetylaspartate (median Cramer-Rao Lower Bound [CRLB] = 3%), glutamate+glutamine (8%), and glutathione (13%). In addition, we demonstrate potential clinical utility of this technique by optimizing the TE to detect 2-hydroxyglutarate (long TE semi-LASER, TE = 110 ms), to produce relevant high-resolution metabolite maps of grade III IDH-mutant oligodendroglioma in a single patient. This study demonstrates the potential utility of MRSI in the clinical setting at 3 Tesla.
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影响因子:
3.3
作者:
Jiang, Wenwen;Lustig, Michael;Larson, Peder E. Z.
通讯作者:
Larson, Peder E. Z.
影响因子:
3.3
作者:
Adalsteinsson, E;Irarrazabal, P;Spielman, DM
通讯作者:
Spielman, DM
影响因子:
11.2
作者:
Emir UE;Larkin SJ;de Pennington N;Voets N;Plaha P;Stacey R;Al-Qahtani K;Mccullagh J;Schofield CJ;Clare S;Jezzard P;Cadoux-Hudson T;Ansorge O
通讯作者:
Ansorge O
影响因子:
3.3
作者:
KLOSE, U
通讯作者:
KLOSE, U
影响因子:
3.3
作者:
Greiser, A;von Kienlin, M
通讯作者:
von Kienlin, M