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 inJournal of magnetic resonance (1997) Vol. 173; no. 1; pp. 169 - 174
Main Authors Knight-Scott, Jack, Dunham, S. Andrea, Shanbhag, Dattesh D.
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.03.2005
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ISSN1090-7807
1096-0856
DOI10.1016/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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Issue 1
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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StartPage 169
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
URI https://dx.doi.org/10.1016/j.jmr.2004.12.001
https://www.ncbi.nlm.nih.gov/pubmed/15705525
https://www.proquest.com/docview/67424410
Volume 173
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