Increasing the speed of relaxometry-based compartmental analysis experiments in STEAM spectroscopy
In this work we present a method for improving the speed of spin–spin relaxation time ( T 2) measurements for compartmental analysis in stimulated echo localized magnetic resonance spectroscopy without reducing the sampling density. The technique uses a progressive repetition time (TR) to compensate...
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Published in | Journal of magnetic resonance (1997) Vol. 173; no. 1; pp. 169 - 174 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
01.03.2005
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Subjects | |
Online Access | Get full text |
ISSN | 1090-7807 1096-0856 |
DOI | 10.1016/j.jmr.2004.12.001 |
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Abstract | In this work we present a method for improving the speed of spin–spin relaxation time (
T
2) measurements for compartmental analysis in stimulated echo localized magnetic resonance spectroscopy without reducing the sampling density. The technique uses a progressive repetition time (TR) to compensate for echo time (TE) dependent variations in saturation effects that would otherwise modulate the received signal at short TRs. The method was validated in
T
2 studies on 10 young healthy subjects in spectroscopic voxels localized along either the right or left Sylvian fissure (2
×
2
×
1.5
cm
3, 10
ms mixing time (TM), 2048 data points, 819.2
ms acquisition time). The TR was automatically adjusted so that TR–TM–TE/2 was kept constant as the TE was incremented. Compared to long TR
T
2 experiments, the progressive TR technique consistently replicated the
T
2 relaxation times and reference signals of the tissue water compartment while reducing the data acquisition time by more than 50%. The percent error was on average less than 2% for estimates of
T
2 and
S
0 for the tissue water, an indication that the progressive TR technique is a useful method for determining the tissue water signal for internal referencing. |
---|---|
AbstractList | In this work we present a method for improving the speed of spin-spin relaxation time (T2) measurements for compartmental analysis in stimulated echo localized magnetic resonance spectroscopy without reducing the sampling density. The technique uses a progressive repetition time (TR) to compensate for echo time (TE) dependent variations in saturation effects that would otherwise modulate the received signal at short TRs. The method was validated in T2 studies on 10 young healthy subjects in spectroscopic voxels localized along either the right or left Sylvian fissure (2 x 2 x 1.5 cm3, 10 ms mixing time (TM), 2048 data points, 819.2 ms acquisition time). The TR was automatically adjusted so that TR-TM-TE/2 was kept constant as the TE was incremented. Compared to long TR T2 experiments, the progressive TR technique consistently replicated the T2 relaxation times and reference signals of the tissue water compartment while reducing the data acquisition time by more than 50%. The percent error was on average less than 2% for estimates of T2 and S(0) for the tissue water, an indication that the progressive TR technique is a useful method for determining the tissue water signal for internal referencing. In this work we present a method for improving the speed of spin-spin relaxation time (T2) measurements for compartmental analysis in stimulated echo localized magnetic resonance spectroscopy without reducing the sampling density. The technique uses a progressive repetition time (TR) to compensate for echo time (TE) dependent variations in saturation effects that would otherwise modulate the received signal at short TRs. The method was validated in T2 studies on 10 young healthy subjects in spectroscopic voxels localized along either the right or left Sylvian fissure (2 x 2 x 1.5 cm3, 10 ms mixing time (TM), 2048 data points, 819.2 ms acquisition time). The TR was automatically adjusted so that TR-TM-TE/2 was kept constant as the TE was incremented. Compared to long TR T2 experiments, the progressive TR technique consistently replicated the T2 relaxation times and reference signals of the tissue water compartment while reducing the data acquisition time by more than 50%. The percent error was on average less than 2% for estimates of T2 and S(0) for the tissue water, an indication that the progressive TR technique is a useful method for determining the tissue water signal for internal referencing.In this work we present a method for improving the speed of spin-spin relaxation time (T2) measurements for compartmental analysis in stimulated echo localized magnetic resonance spectroscopy without reducing the sampling density. The technique uses a progressive repetition time (TR) to compensate for echo time (TE) dependent variations in saturation effects that would otherwise modulate the received signal at short TRs. The method was validated in T2 studies on 10 young healthy subjects in spectroscopic voxels localized along either the right or left Sylvian fissure (2 x 2 x 1.5 cm3, 10 ms mixing time (TM), 2048 data points, 819.2 ms acquisition time). The TR was automatically adjusted so that TR-TM-TE/2 was kept constant as the TE was incremented. Compared to long TR T2 experiments, the progressive TR technique consistently replicated the T2 relaxation times and reference signals of the tissue water compartment while reducing the data acquisition time by more than 50%. The percent error was on average less than 2% for estimates of T2 and S(0) for the tissue water, an indication that the progressive TR technique is a useful method for determining the tissue water signal for internal referencing. In this work we present a method for improving the speed of spin–spin relaxation time ( T 2) measurements for compartmental analysis in stimulated echo localized magnetic resonance spectroscopy without reducing the sampling density. The technique uses a progressive repetition time (TR) to compensate for echo time (TE) dependent variations in saturation effects that would otherwise modulate the received signal at short TRs. The method was validated in T 2 studies on 10 young healthy subjects in spectroscopic voxels localized along either the right or left Sylvian fissure (2 × 2 × 1.5 cm 3, 10 ms mixing time (TM), 2048 data points, 819.2 ms acquisition time). The TR was automatically adjusted so that TR–TM–TE/2 was kept constant as the TE was incremented. Compared to long TR T 2 experiments, the progressive TR technique consistently replicated the T 2 relaxation times and reference signals of the tissue water compartment while reducing the data acquisition time by more than 50%. The percent error was on average less than 2% for estimates of T 2 and S 0 for the tissue water, an indication that the progressive TR technique is a useful method for determining the tissue water signal for internal referencing. |
Author | Shanbhag, Dattesh D. Knight-Scott, Jack Dunham, S. Andrea |
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Keywords | Spin–spin relaxation Spin–lattice relaxation Transverse relaxation T 2 MRS |
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Snippet | In this work we present a method for improving the speed of spin–spin relaxation time (
T
2) measurements for compartmental analysis in stimulated echo... In this work we present a method for improving the speed of spin-spin relaxation time (T2) measurements for compartmental analysis in stimulated echo localized... |
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SubjectTerms | Adolescent Adult Brain Chemistry Female Humans Magnetic Resonance Spectroscopy - methods Male MRS Signal Processing, Computer-Assisted Spin–lattice relaxation Spin–spin relaxation Transverse relaxation Water - analysis |
Title | Increasing the speed of relaxometry-based compartmental analysis experiments in STEAM spectroscopy |
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