Human brain-structure resolved T(2) relaxation times of proton metabolites at 3 Tesla.

The transverse relaxation times, T(2), of N-acetylaspartate (NAA), total choline (Cho), and creatine (Cr) obtained at 3T in several human brain regions of eight healthy volunteers are reported. They were obtained simultaneously in 320 voxels with three-dimensional (3D) proton MR spectroscopy ((1)H-MRS) at 1 cm(3) spatial resolution. A two-point protocol, optimized for the least error per given time by adjusting both the echo delay (TE(i)) and number of averages, N(i), at each point, was used. Eight healthy subjects (four males and four females, age = 26 +/- 2 years) underwent the hour-long procedure of four 15-min, 3D acquisitions (TE(1) = 35 ms, N(1) = 1; and TE(2) = 285 ms, N(2) = 3). The results reveal that across all subjects the NAA and Cr T(2)s in gray matter (GM) structures (226 +/- 17 and 137 +/- 12 ms, respectively) were 13-17% shorter than the corresponding T(2)s in white matter (WM; 264 +/- 10 and 155 +/- 7 ms, respectively). The T(2)s of Cho did not differ between GM and WM (207 +/- 17 and 202 +/- 8, respectively). For the purpose of metabolic quantification, these values justify to within +/-10% the previous use of one T(2) per metabolite for 1) the entire brain and 2) all subjects. These T(2) values (which to our knowledge were obtained for the first time at this field, spatial resolution, coverage, and precision) are essential for reliable absolute metabolic quantification.     

Measuring the longitudinal relaxation time of GABA in vivo at 3 tesla

Purpose:

To measure the in vivo longitudinal relaxation time T1 of GABA at 3 Tesla (T).

Materials and Methods:

J‐difference edited single‐voxel MR spectroscopy was used to isolate γ‐aminobutyric acid (GABA) signals. An increased echo time (80 ms) acquisition was used, accommodating the longer, more selective editing pulses required for symmetric editing‐based suppression of co‐edited macromolecular signal. Acquiring edited GABA measurements at a range of relaxation times in 10 healthy participants, a saturation‐recovery equation was used to model the integrated data.

Results:

The longitudinal relaxation time of GABA was measured as T_1,GABA = 1.31 ± 0.16 s.

Conclusion:

The method described has been successfully applied to measure the T1 of GABA in vivo at 3T. J. Magn. Reson. Imaging 2013;37:999–1003. © 2012 Wiley Periodicals, Inc.     

Sodium long‐component T mapping in human brain at 7 Tesla

Sodium (²³Na) MRI may provide unique information about the cellular and metabolic integrity of the brain. The quantification of tissue sodium concentration from ²³Na images with nonzero echo time (TE) requires knowledge of tissue‐specific parameters that influence the single‐quantum sodium signal such as transverse (T₂) relaxation times. We report the sodium (²³Na) long component of the effective transverse relaxation time T values obtained at 7 T in several brain regions from six healthy volunteers. A two‐point protocol based on a gradient‐echo sequence optimized for the least error per given imaging time was used (TE₁ = 12 ms; TE₂ = 37 ms; averaged N₁ = 5; N₂ = 15 times; pulse repetition time = 130 ms). The results reveal that long T component of tissue sodium (mean ± standard deviation) varied between cerebrospinal fluid (54 ± 4 ms) and gray (28 ± 2 ms) and white (29 ± 2 ms) matter structures. The results also show that the long T component increases as a function of the main static field B₀, indicating that correlation time of sodium ion motion is smaller than the time‐scale defined by the Larmor frequency. These results are a prerequisite for the quantification of tissue sodium concentration from ²³Na MRI scans with nonzero echo time, will contribute to the design of future measurements (such as triple‐quantum imaging), and themselves may be of clinical utility. Magn Reson Med, 2009. © 2009 Wiley‐Liss, Inc.     

Myocardial T2 quantitation in patients with iron overload at 3 Tesla

Purpose

To investigate the feasibility of measuring myocardial T2 at 3 Tesla for assessment of tissue iron in thalassemia major and other iron overloaded patients.

Materials and Methods

A single‐breathhold electrocardiogram‐triggered black‐blood multi‐echo spin‐echo (MESE) sequence with a turbo factor of 2 was implemented at 3 Tesla (T). Myocardial and liver T2 values were measured with three repeated breathholds in 8 normal subjects and 24 patients. Their values, together with the T2* values measured using a breathhold multi‐echo gradient‐echo sequence, were compared with those at 1.5T in the same patients.

Results

At 3T, myocardial T2 was found to be 39.6 ± 7.4 ms in normal subjects. In patients, it ranged from 12.9 to 50.1 ms. T2 and T2* were observed to correlate in heart (ρ = 0.93, ρ < 0.0001) and liver (P = 0.95, P < 0.0001). Myocardial T2 and T2* at 3T were also highly correlated with the 1.5T measurements. Preliminary results indicated that myocardial T2 quantitation was relatively insensitive to B1 variation, and reproducible with 3.2% intra‐exam and 3.8% inter‐exam variations.

Conclusion

Myocardial T2 quantitation is feasible at 3T. Given the substantially decreased T2* and increased B0 inhomogeneity, the rapid myocardial T2 measurement protocol demonstrated here may present a robust alternative to study cardiac iron overload at 3T. J. Magn. Reson. Imaging 2009;30:394–400. © 2009 Wiley‐Liss, Inc.     

Improved in vivo measurement of myocardial transverse relaxation with 3 Tesla magnetic resonance imaging

Purpose

To develop practical methods at 3 Tesla (T) for measuring myocardial transverse relaxation in normal human myocardium.

Materials and Methods

Ten healthy volunteers were investigated with four multi‐echo, turbo spin‐echo (TSE) methods. Each method traded acquired phase encoding lines per image for echo‐image sample points obtained along the T₂ decay curve. Four multi‐echo turbo field‐echo (TFE) methods were also tested. The TFE methods highlighted differences between achievable receiver bandwidth and echo time constraints versus the number of sample points obtained along the T decay curve.

Results

Measured transverse relaxation values were consistent in reported means across all scan methods. T₂ for the ventricular septum was measured as 58.8 ± 7.7 ms (N = 10). T for the ventricular septum was 31.6 ± 5.8 ms (N = 10). The variation of mean T₂ or T within an region of interest improved significantly with increases in acquired echoes. Therefore, four or more echoes may provide for clear distinctions between regions of altered tissue composition within a subject.

Conclusion

These results suggest that the 4‐echo methods are best suited for measuring variations in transverse relaxation values in the mid‐ventricular septum. J. Magn. Reson. Imaging 2009;30:684–689. © 2009 Wiley‐Liss, Inc.     

Age dependence of regional proton metabolites T2 relaxation times in the human brain at 3 T

Although recent studies indicate that use of a single global transverse relaxation time, T₂, per metabolite is sufficient for better than ±10% quantification precision at intermediate and short echo‐time spectroscopy in young adults, the age‐dependence of this finding is unknown. Consequently, the age effect on regional brain choline (Cho), creatine (Cr), and N‐acetylaspartate (NAA) T₂s was examined in four age groups using 3D (four slices, 80 voxels 1 cm³ each) proton MR spectroscopy in an optimized two‐point protocol. Metabolite T₂s were estimated in each voxel and in 10 gray and white matter (GM, WM) structures in 20 healthy subjects: four adolescents (13 ± 1 years old), eight young adults (26 ± 1); two middle‐aged (51 ± 6), and six elderly (74 ± 3). The results reveal that T₂s in GM (average ± standard error of the mean) of adolescents (NAA: 301 ± 30, Cr: 162 ± 7, Cho: 263 ± 7 ms), young adults (NAA: 269 ± 7, Cr: 156 ± 7, Cho: 226 ± 9 ms), and elderly (NAA: 259 ± 13, Cr: 154 ± 8, Cho: 229 ± 14 ms), were 30%, 16%, and 10% shorter than in WM, yielding mean global T₂s of NAA: 343, Cr: 172, and Cho: 248 ms. The elderly NAA, Cr, and Cho T₂s were 12%, 6%, and 10% shorter than the adolescents, a change of under 1 ms/year assuming a linear decline with age. Formulae for T₂ age‐correction for higher quantification precision are provided. Magn Reson Med 60:790–795, 2008. © 2008 Wiley‐Liss, Inc.     

Metabolite proton T2 mapping in the healthy rhesus macaque brain at 3 T

The structure and metabolism of the rhesus macaque brain, an advanced model for neurologic diseases and their treatment response, is often studied noninvasively with MRI and ¹H‐MR spectroscopy. Due to the shorter transverse relaxation time (T₂) at the higher magnetic fields these studies favor, the echo times used in ¹H‐MR spectroscopy subject the metabolites to unknown T₂ weighting, decreasing the accuracy of quantification which is key for inter‐ and intra‐animal comparisons. To establish the “baseline” (healthy animal) T₂ values, we mapped them for the three main metabolites' T₂s at 3 T in four healthy rhesus macaques and tested the hypotheses that their mean values are similar (i) among animals; and (ii) to analogs regions in the human brain. This was done with three‐dimensional multivoxel ¹H‐MR spectroscopy at (0.6 × 0.6 × 0.5 cm)³ = 180 μL spatial resolution over a 4.2 × 3.0 × 2.0 = 25 cm³ (～30%) of the macaque brain in a two‐point protocol that optimizes T₂ precision per unit time. The estimated T₂s in several gray and white matter regions are all within 10% of those reported in the human brain (mean ± standard error of the mean): N‐acetylaspartate = 316 ± 7, creatine = 177 ± 3, and choline = 264 ± 9 ms, with no statistically significant gray versus white matter differences. Magn Reson Med, 2009. © 2009 Wiley‐Liss, Inc.     

Brain metabolites B1‐corrected proton T1 mapping in the rhesus macaque at 3 T

The accuracy of metabolic quantification in MR spectroscopy is limited by the unknown radiofrequency field and T₁. To address both issues in proton (¹H) MR spectroscopy, we obtained radiofrequency field–corrected T₁ maps of N‐acetylaspartate, choline, and creatine in five healthy rhesus macaques at 3 T. For efficient use of the 4 hour experiment, we used a new three‐point protocol that optimizes the precision of T₁ in three‐dimensional ¹H‐MR spectroscopy localization for extensive, ～30%, brain coverage at 0.6 × 0.6 × 0.5 cm³ = 180‐μL spatial resolution. The resulting mean T₁s in 700 voxels were N‐acetylaspartate = 1232 ± 44, creatine = 1238 ± 23 and choline = 1107 ± 56 ms (mean ± standard error of the mean). Their histograms from all 140 voxels in each animal were similar in position and shape, characterized by standard errors of the mean of the full width at half maximum divided by their means of better than 8%. Regional gray matter N‐acetylaspartate, choline, and creatine T₁s (1333 ± 43, 1265 ± 52, and 1131 ± 28 ms) were 5–10% longer than white matter: 1188 ± 34, 1201 ± 24, and 1082 ± 50 ms (statistically significant for the N‐acetylaspartate only), all within 10% of the corresponding published values in the human brain. Magn Reson Med 63:865–871, 2010. © 2010 Wiley‐Liss, Inc.     

Effect of multislice acquisition on T1 and T2 measurements of articular cartilage at 3T

PURPOSE: The aim of this study was to investigate the effect of magnetization transfer on multislice T1 and T2 measurements of articular cartilage. MATERIALS AND METHODS: A set of phantoms with different concentrations of collagen and contrast agent (Gd-DTPA2-) were used for the in vitro study. A total of 20 healthy knees were used for the in vivo study. T1 and T2 measurements were performed using fast-spin-echo inversion-recovery (FSE-IR) sequence and multi-spin-echo (MSE) sequence, respectively, in both in vitro and in vivo studies. We investigated the difference in T1 and T2 values between that measured by single-slice acquisition and that measured by multislice acquisition. RESULTS: Regarding T1 measurement, a large drop of T1 in all slices and also a large interslice variation in T1 were observed when multislice acquisition was used. Regarding T2 measurement, a substantial drop of T2 in all slices was observed; however, there was no apparent interslice variation when multislice acquisition was used. CONCLUSION: This study demonstrated that the adaptation of multislice acquisition technique for T1 measurement using FSE-IR methodology is difficult and its use for clinical evaluation is problematic. In contrast, multislice acquisition for T2 measurement using MSE was clinically applicable if inaccuracies caused by multislice acquisition were taken into account.     

In vivo detection of GABA in human brain using a localized double-quantum filter technique

A proton MR spectral editing technique employing a spatially localized, double-quantum filter (DQF) was used to measure γ-aminobutyric acid (GABA) in the human brain at 1.5 T. The double-quantum method provided robust, single-shot suppression of uncoupled resonances from choline, creatine, and NAA and allowed detection of the γCH₂ GABA (3.0 ppm) resonance with 30% efficiency. Spatial localization of the GABA measurement was achieved by incorporating PRESS localization within the double-quantum excitation and detection sequence. A calibration technique was developed to adjust the relative phases of the RF pulses to maximize the in vivo double-quantum detection efficiency for an arbitrary voxel location. The sequence efficiency, degree of suppression of uncoupled resonances, and characterization of the in vivo DQF technique was examined in phantom experiments and in a study of the occipital lobe of 10 normal subjects. The ratio of the 3.0-ppm GABA resonance to the 3.0-ppm creatine resonance was found to be 0.20 ± 0.05 (SD).