Assessment of 3D proton MR echo-planar spectroscopic imaging using automated spectral analysis
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作者:
Ebel, A
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Univ Calif San Francisco, MR Unit, DVA Med Ctr, Dept Radiol, San Francisco, CA 94121 USAUniv Calif San Francisco, MR Unit, DVA Med Ctr, Dept Radiol, San Francisco, CA 94121 USA
Ebel, A
[1
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Soher, BJ
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Univ Calif San Francisco, MR Unit, DVA Med Ctr, Dept Radiol, San Francisco, CA 94121 USAUniv Calif San Francisco, MR Unit, DVA Med Ctr, Dept Radiol, San Francisco, CA 94121 USA
Soher, BJ
[1
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Maudsley, AA
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Univ Calif San Francisco, MR Unit, DVA Med Ctr, Dept Radiol, San Francisco, CA 94121 USAUniv Calif San Francisco, MR Unit, DVA Med Ctr, Dept Radiol, San Francisco, CA 94121 USA
Maudsley, AA
[1
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机构:
[1] Univ Calif San Francisco, MR Unit, DVA Med Ctr, Dept Radiol, San Francisco, CA 94121 USA
For many clinical applications of proton MR spectroscopic imaging (MRSI) of the brain, diagnostic assessment is limited by insufficient coverage provided by single- or multislice acquisition methods as well as by the use of volume preselection methods. Additionally, traditional spectral analysis methods may limit the operator to detailed analysis of only a few selected brain regions. It is therefore highly desirable to use a fully 3D approach, combined with spectral analysis procedures that enable automated assessment of 3D metabolite distributions over the whole brain. In this study, a 3D echo-planar MRS[ technique has been implemented without volume preselection to provide sufficient spatial resolution with maximum coverage of the brain. Using MRSI acquisitions in normal subjects at 1.5T and a fully automated spectral analysis procedure, an assessment of the resultant spectral quality and the extent of viable data in human brain was carried out. The analysis found that 69% of brain voxels were obtained with acceptable spectral quality at TE = 135 ms, and 52% at TE = 25 ms. Most of the rejected voxels were located near the sinuses or temporal bones and demonstrated poor B-o homogeneity and additional regions were affected by stronger lipid contamination at TE = 25 ms. (C) 2001 Wiley-Liss, Inc.
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Univ Calif Los Angeles, Radiol Sci, Los Angeles, CA 90095 USAUniv Calif Los Angeles, Radiol Sci, Los Angeles, CA 90095 USA
Nagarajan, Rajakumar
Carpenter, Catherine L.
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UCLA, Sch Nursing, Los Angeles, CA 90024 USA
UCLA, Sch Med, Los Angeles, CA USA
UCLA, Sch Publ Hlth, Los Angeles, CA 90024 USAUniv Calif Los Angeles, Radiol Sci, Los Angeles, CA 90095 USA
Carpenter, Catherine L.
Lee, Cathy C.
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VA Greater Los Angeles Healthcare Syst, Geriatr Res Educ & Clin Ctr, Los Angeles, CA USA
UCLA, Dept Med, Los Angeles, CA 90024 USAUniv Calif Los Angeles, Radiol Sci, Los Angeles, CA 90095 USA
Lee, Cathy C.
Michael, Navin
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Singapore Inst Clin Sci, Singapore, SingaporeUniv Calif Los Angeles, Radiol Sci, Los Angeles, CA 90095 USA
Michael, Navin
Sarma, Manoj K.
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Univ Calif Los Angeles, Radiol Sci, Los Angeles, CA 90095 USAUniv Calif Los Angeles, Radiol Sci, Los Angeles, CA 90095 USA
Sarma, Manoj K.
Souza, Raissa
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Univ Calif Los Angeles, Radiol Sci, Los Angeles, CA 90095 USAUniv Calif Los Angeles, Radiol Sci, Los Angeles, CA 90095 USA
Souza, Raissa
Xu, Edward
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Univ Calif Los Angeles, Radiol Sci, Los Angeles, CA 90095 USAUniv Calif Los Angeles, Radiol Sci, Los Angeles, CA 90095 USA
Xu, Edward
Velan, S. Sendhil
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Singapore Bioimaging Consortium, Lab Mol Imaging, Singapore, Singapore
Natl Univ Singapore, Dept Physiol, Singapore, Singapore
Natl Univ Singapore, Dept Med, Singapore, SingaporeUniv Calif Los Angeles, Radiol Sci, Los Angeles, CA 90095 USA
Velan, S. Sendhil
Hahn, Theodore J.
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VA Greater Los Angeles Healthcare Syst, Geriatr Res Educ & Clin Ctr, Los Angeles, CA USA
UCLA, Dept Med, Los Angeles, CA 90024 USAUniv Calif Los Angeles, Radiol Sci, Los Angeles, CA 90095 USA
Hahn, Theodore J.
Go, Vay-Liang
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UCLA, Dept Med, Los Angeles, CA 90024 USAUniv Calif Los Angeles, Radiol Sci, Los Angeles, CA 90095 USA
Go, Vay-Liang
Thomas, M. Albert
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Univ Calif Los Angeles, Radiol Sci, Los Angeles, CA 90095 USAUniv Calif Los Angeles, Radiol Sci, Los Angeles, CA 90095 USA