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Metabolite Resonances (metabolite + resonance)

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Medical Sciences100%

Selected Abstracts

Proton spectroscopic metabolite signal relaxation times in preterm infants: A prerequisite for quantitative spectroscopy in infant brain

JOURNAL OF MAGNETIC RESONANCE IMAGING, Issue 6 2003
Harald Kugel PhD
Abstract Purpose To determine relaxation times of metabolite signals in proton magnetic resonance (MR) spectra of immature brain, which allow a correction of relaxation that is necessary for a quantitative evaluation of spectra acquired with long TE. Proton MR spectra acquired with long TE allow a better definition of metabolites as N-acetyl aspartate (NAA) and lactate especially in children. Materials and Methods Relaxation times were determined in the basal ganglia of 84 prematurely born infants at a postconceptional age of 37.8 ± 2.2 (mean ± SD) weeks. Metabolite resonances were investigated using the double-spin-echo volume selection method (PRESS) at 1.5 T. T1 was determined from intensity ratios of signals obtained with TRs of 1884 and 6000 msec, measured at 3 TEs (25 msec, 136 msec, 272 msec). T2 was determined from signal intensity ratios obtained with TEs of 136 msec and 272 msec, measured at 2 TR. Taking only long TEs reduced baseline distortions by macromolecules and lipids. For myo-inositol (MI), an apparent T2 for short TE was determined from the ratio of signals obtained with TE = 25 msec and 136 msec. Intensities were determined by fitting a Lorentzian to the resonance, and by integration. Results Relaxation times were as follows: trimethylamine-containing compounds (Cho): T1 = 1217 msec/T2 = 273 msec; total creatine (Cr) at 3.9 ppm: 1010 msec/111 msec; Cr at 3.0 ppm: 1388 msec/224 msec; NAA: 1171 msec/499 msec; Lac: 1820 msec/1022 msec; MI: 1336 msec/173 msec; apparent T2 at short TE: 68 msec. Conclusion T1 and T2 in the basal ganglia of premature infants do not differ much from previously published data from basal ganglia of older children and adults. T2 of Cho was lower than previous values. T2 of Cr at 3.9 ppm and Lac have been measured under different conditions before, and present values differ from these data. J. Magn. Reson. Imaging 2003;17:634,640. © 2003 Wiley-Liss, Inc. [source]

In vivo proton spectroscopy without solvent suppression

CONCEPTS IN MAGNETIC RESONANCE, Issue 4 2001
David B. Clayton
Abstract In 1H MR spectroscopy of the human brain, it is common practice to suppress the solvent signal prior to acquisition. This reduces the large dynamic range which is otherwise required of the MR receiver and digitizer in order to detect the dilute metabolite resonances in the presence of the much larger water signal. However, complete solvent suppression is not always obtainable, particularly over large volumes and in superficial regions containing large susceptibility gradients. In this work, it demonstrated that modern commercial MR scanners possess the dynamic range necessary to adequately resolve the 1H metabolites in unsuppressed spectra. Moreover, a postacquisition method is presented which can completely remove the intact water signal and accurately quantitate the metabolite peaks. Preserving the water signal in in vivo spectroscopy has several useful benefits, such as providing a high signal-to-noise ratio internal concentration, frequency, and line shape reference. Comparison is made between suppressed and unsuppressed spectra from both a phantom and the human brain acquired at 4 T. © 2001 John Wiley & Sons, Inc. Concepts Magn Reson 13: 260,275, 2001 [source]

Comparison of spectral fitting methods for overlapping J-coupled metabolite resonances

MAGNETIC RESONANCE IN MEDICINE, Issue 3 2010
A. Gonenc
Abstract There is increasing interest in the use of two-dimensional J-resolved spectroscopic acquisition (multiecho) methods for in vivo proton magnetic resonance spectroscopy due to the improved discrimination of overlapping J-coupled multiplet resonances that is provided. Of particular interest is the potential for discrimination of the overlapping resonances of glutamate and glutamine. In this study, a new time-domain parametric spectral model that makes use of all available data is described for fitting the complete two-dimensional multiecho data, and the performance of this method was compared with fitting of one-dimensional spectra obtained following averaging multiecho data (echo time-averaged) and single-echo time PRESS (Point Resolved Spectroscopy) acquired spectra. These methods were compared using data obtained from a phantom containing typical brain metabolites and a human brain. Results indicate that improved performance and accuracy is obtained for the two-dimensional acquisition and spectral fitting model. Magn Reson Med, 2010. © 2010 Wiley-Liss, Inc. [source]

Eliminating spurious lipid sidebands in 1H MRS of breast lesions

MAGNETIC RESONANCE IN MEDICINE, Issue 2 2002
Patrick J. Bolan
Abstract Detecting metabolites in breast lesions by in vivo 1H MR spectroscopy can be difficult due to the abundance of mobile lipids in the breast which can produce spurious sidebands that interfere with the metabolite signals. Two-dimensional J -resolved spectroscopy has been demonstrated in the brain as a means to eliminate these artifacts from a large water signal; coherent sidebands are resolved at their natural frequencies, leaving the noncoupled metabolite resonances in the zero-frequency trace of the 2D spectrum. This work demonstrates that using the zero-frequency trace,or equivalently the average of spectra acquired with different echo times,can be used to separate noncoupled metabolite signals from the lipid-induced sidebands. This technique is demonstrated with simulations, phantom studies, and in several breast lesions. Compared to the conventional approach using a single echo time, echo time averaging provides increased sensitivity for the study of small and irregularly shaped lesions. Magn Reson Med 48:215,222, 2002. © 2002 Wiley-Liss, Inc. [source]