Multiple gradient echo sequence optimized for rapid, single-scan mapping of R*2 at high B0

被引:31
作者
Wild, JM
Martin, WRW
Allen, PS
机构
[1] Univ Alberta, Dept Biomed Engn, Edmonton, AB, Canada
[2] Univ Alberta, Dept Neurol, Edmonton, AB, Canada
[3] Univ Sheffield, Unit Acad Radiol, Sheffield S10 2FJ, S Yorkshire, England
关键词
2D gradient echo; susceptibility; artifact; R-2(*); inhomogeneity;
D O I
10.1002/mrm.10291
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 [临床医学]; 100207 [影像医学与核医学]; 1009 [特种医学];
摘要
A multiple-gradient-echo sequence is proposed for accurately mapping R-2(*) in the presence of in-slice macroscopic susceptibility gradients. In-slice signal loss caused by background macroscopic susceptibility gradients is mitigated by combining three successive gradient-echo images whose slice refocus gradients are successively incremented. The optimum incrementation of slice-refocusing gradients was determined by numerical simulation. By repeating further cycles of three images in the same sequence, artifact-compensated data spanning a range of echo times (TEs) was acquired leading to single-scan, R-2(*) maps that are quantitatively reflective of microscopic field inhomogeneities. The performance of the sequence was demonstrated at 3.0T, first with a doped aqueous phantom, and then on the head of a normal volunteer. That performance is compared quantitatively with previously published work. (C) 2002 Wiley-Liss, Inc.
引用
收藏
页码:867 / 876
页数:10
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