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Slice-selective adiabatic magnetization T2 -preparation (SAMPA) for efficient T2 -weighted imaging at ultrahigh field strengths.

ABSTRACT: At high field, T2 -weighted (T2 w) imaging is limited by transmit field inhomogeneity and increased radiofrequency power deposition. In this work, we introduce SAMPA (Slice-selective Adiabatic Magnetization T2 PrepAration) and demonstrate its use for efficient brain T2 w imaging at 7 Tesla (T).SAMPA was designed by subsampling an optimized B1 insensitive rotation (BIR4) waveform with small tip angle linear subpulses. To perform T2 w imaging, SAMPA was inserted before a fast gradient echo acquisition. The off-resonance behavior, B1 robustness, and slice selectivity of the novel T2 preparation module were analyzed using Bloch simulations. The performance of SAMPA for T2 w imaging was demonstrated in phantom experiments as well as in the brains of healthy volunteers at 7T.Based on simulations, the proposed design operates at peak B1 of 15 ?T and higher, within a 400 Hz bandwidth. T2 values were in strong agreement with spin echo-based T2 mapping in phantom experiments. Whole brain, interleaved multislab three-dimensional imaging could be acquired with 0.8 mm3 isotropic resolution in 5:36 min per T2 weighting.Compared with previous adiabatic T2 preparation techniques, SAMPA allows for slice-selectivity, which can lead to efficient and robust acquisitions for T2 w imaging at high field. Magn Reson Med 76:1741-1749, 2016. © 2015 International Society for Magnetic Resonance in Medicine.

SUBMITTER: Dyvorne H

PROVIDER: S-EPMC4887419 | biostudies-literature | 2016 Dec

REPOSITORIES: biostudies-literature

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Slice-selective adiabatic magnetization T<sub>2</sub> -preparation (SAMPA) for efficient T<sub>2</sub> -weighted imaging at ultrahigh field strengths.

Dyvorne Hadrien H Balchandani Priti P

Magnetic resonance in medicine 20151201 6

<h4>Purpose</h4>At high field, T<sub>2</sub> -weighted (T<sub>2</sub> w) imaging is limited by transmit field inhomogeneity and increased radiofrequency power deposition. In this work, we introduce SAMPA (Slice-selective Adiabatic Magnetization T<sub>2</sub> PrepAration) and demonstrate its use for efficient brain T<sub>2</sub> w imaging at 7 Tesla (T).<h4>Methods</h4>SAMPA was designed by subsampling an optimized B<sub>1</sub> insensitive rotation (BIR4) waveform with small tip angle linear sub ...[more]

PMID: 26619960

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Project description:PurposeTo develop and evaluate a free-breathing slice-interleaved T2 mapping sequence by proposing a new slice-selective T2 magnetization preparation (T2 prep) sequence that allows interleaved data acquisition for different slices in subsequent heartbeats.MethodsWe developed a slice-selective T2 prep for myocardial T2 mapping by adding slice-selective gradients to a conventional single-slice T2 prep sequence. In this sequence, five slices are acquired during five consecutive heartbeats, each using a slice-selective T2 prep. The scheme was repeated four times using different T2 prep echo times. We compared the performance of the proposed slice-interleaved T2 mapping sequence and the conventional single-slice T2 mapping sequence in term of accuracy, precision, and reproducibility using phantom experiments and in vivo imaging in 10 healthy subjects. We also evaluated the feasibility of the proposed sequence in 28 patients with cardiovascular disease, and the quality of the maps was scored subjectively. Furthermore, we investigated the impact of through-plane motion by comparing T2 measurements acquired during end-systole versus mid-diastole.ResultsT2 measurements using a slice-interleaved T2 mapping sequence were correlated with a spin echo (r(2) = 0.88) and single-slice T2 mapping sequence (r(2) = 0.98). The mean myocardial T2 values were correlated between slice-interleaved (48 ms) and single-slice (51 ms) T2 mapping sequences. Subjective scores of T2 map quality were good to excellent in 81% of the maps in patients. There was no difference in T2 measurements between end-systole versus mid-diastole.ConclusionsThe proposed free-breathing slice-interleaved T2 mapping sequence allows T2 measurements of five left ventricular slices in 20 heartbeats with similar reproducibility and precision as the single-slice T2 mapping sequence but with a four-fold reduction in acquisition time. Magn Reson Med 76:555-565, 2016. © 2015 Wiley Periodicals, Inc.

Project description:BackgroundChemotherapy-induced cardiotoxicity is a well-recognized adverse effect of chemotherapy. Quantitative T1-mapping cardiovascular magnetic resonance (CMR) is useful for detecting subclinical myocardial changes in anthracycline-induced cardiotoxicity. The aim of the present study was to histopathologically validate the T1 and T2 mapping parameters for the evaluation of diffuse myocardial changes in rat models of cardiotoxicity.MethodsRat models of cardiotoxicity were generated by injecting rats with doxorubicin (1 mg/kg, twice a week). CMR was performed with a 9.4 T ultrahigh-field scanner using cine, pre-T1, post-T1 and T2 mapping sequences to evaluate the left ventricular ejection fraction (LVEF), native T1, T2, and extracellular volume fraction (ECV). Histopathological examinations were performed and the association of histopathological changes with CMR parameters was assessed.ResultsFive control rats and 36 doxorubicin-treated rats were included and classified into treatment periods. In the doxorubicin-treated rats, the LVEF significantly decreased after 12 weeks of treatment (control vs. 12-week treated: 73 ± 4% vs. 59 ± 9%, P = 0.01). Increased native T1 and ECV were observed after 6 weeks of treatment (control vs. 6-week treated: 1148 ± 58 ms, 14.3 ± 1% vs. 1320 ± 56 ms, 20.3 ± 3%; P = 0.005, < 0.05, respectively). T2 values also increased by six weeks of treatment (control vs. 6-week treated: 16.3 ± 2 ms vs. 10.3 ± 1 ms, P < 0.05). The main histopathological features were myocardial injury, interstitial fibrosis, inflammation, and edema. The mean vacuolar change (%), fibrosis (%), and inflammation score were significantly higher in 6-week treated rats than in the controls (P = 0.03, 0.03, 0.02, respectively). In the univariable analysis, vacuolar change showed the highest correlation with native T1 value (R = 0.60, P < 0.001), and fibrosis showed the highest correlation with ECV value (R = 0.78, P < 0.001). In the multiple linear regression analysis model, vacuolar change was a significant factor for change in native T1 (P = 0.01), and vacuolar change and fibrosis were significant factors for change in ECV (P = 0.006, P < 0.001, respectively) by adding other histopathological parameters (i.e., inflammation and edema scores) CONCLUSIONS: Quantitative T1 and T2 mapping CMR is a useful non-invasive tool reflecting subclinical histopathological changes in anthracycline-induced cardiotoxicity.

Dataset Information

Slice-selective adiabatic magnetization T2 -preparation (SAMPA) for efficient T2 -weighted imaging at ultrahigh field strengths.

Publications

Slice-selective adiabatic magnetization T<sub>2</sub> -preparation (SAMPA) for efficient T<sub>2</sub> -weighted imaging at ultrahigh field strengths.

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