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SAturation-recovery and Variable-flip-Angle-based three-dimensional free-breathing cardiovascular magnetic resonance T1 mapping at 3 T.
Guo, Rui; Si, Dongyue; Chen, Zhensen; Dai, Erpeng; Chen, Shuo; Herzka, Daniel A; Luo, Jianwen; Ding, Haiyan.
Afiliação
  • Guo R; Center for Biomedical Imaging Research, Department of Biomedical Engineering, School of Medicine, Tsinghua University, Beijing, China.
  • Si D; School of Medical Technology, Beijing Institute of Technology, Beijing, China.
  • Chen Z; Center for Biomedical Imaging Research, Department of Biomedical Engineering, School of Medicine, Tsinghua University, Beijing, China.
  • Dai E; Center for Biomedical Imaging Research, Department of Biomedical Engineering, School of Medicine, Tsinghua University, Beijing, China.
  • Chen S; Department of Radiology, Stanford University, Stanford, California, USA.
  • Herzka DA; Center for Biomedical Imaging Research, Department of Biomedical Engineering, School of Medicine, Tsinghua University, Beijing, China.
  • Luo J; National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, Maryland, USA.
  • Ding H; Center for Biomedical Imaging Research, Department of Biomedical Engineering, School of Medicine, Tsinghua University, Beijing, China.
NMR Biomed ; 35(9): e4755, 2022 09.
Article em En | MEDLINE | ID: mdl-35485432
The purpose of the current study was to develop and validate a three-dimensional (3D) free-breathing cardiac T1 -mapping sequence using SAturation-recovery and Variable-flip-Angle (SAVA). SAVA sequentially acquires multiple electrocardiogram-triggered volumes using a multishot spoiled gradient-echo sequence. The first volume samples the equilibrium signal of the longitudinal magnetization, where a flip angle of 2° is used to reduce the time for the magnetization to return to equilibrium. The succeeding three volumes are saturation prepared with variable delays, and are acquired using a 15° flip angle to maintain the signal-to-noise ratio. A diaphragmatic navigator is used to compensate the respiratory motion. T1 is calculated using a saturation-recovery model that accounts for the flip angle. We validated SAVA by simulations, phantom, and human subject experiments at 3 T. SAVA was compared with modified Look-Locker inversion recovery (MOLLI) and saturation-recovery single-shot acquisition (SASHA) in vivo. In phantoms, T1 by SAVA had good agreement with the reference (R2 = 0.99). In vivo 3D T1 mapping by SAVA could achieve an imaging resolution of 1.25 × 1.25 × 8 mm3 . Both global and septal T1 values by SAVA (1347 ± 37 and 1332 ± 42 ms) were in between those by SASHA (1612 ± 63 and 1618 ± 51 ms) and MOLLI (1143 ± 59 and 1188 ± 65 ms). According to the standard deviation (SD) and coefficient of variation (CV), T1 precision measured by SAVA (SD: 99 ± 14 and 60 ± 8 ms; CV: 7.4% ± 0.9% and 4.5% ± 0.6%) was comparable with MOLLI (SD: 99 ± 25 and 46 ± 12 ms; CV: 8.8% ± 2.5% and 3.9% ± 1.1%) and superior to SASHA (SD: 222 ± 89 and 132 ± 33 ms; CV: 13.8% ± 5.5% and 8.1% ± 2.0%). It was concluded that the proposed free-breathing SAVA sequence enables more efficient 3D whole-heart T1 estimation with good accuracy and precision.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Interpretação de Imagem Assistida por Computador / Coração Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Interpretação de Imagem Assistida por Computador / Coração Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article