Literature DB >> 30320945

Multipathway multi-echo (MPME) imaging: all main MR parameters mapped based on a single 3D scan.

Cheng-Chieh Cheng1, Frank Preiswerk1, W Scott Hoge1, Tai-Hsin Kuo2, Bruno Madore1.   

Abstract

PURPOSE: Quantitative parameter maps, as opposed to qualitative grayscale images, may represent the future of diagnostic MRI. A new quantitative MRI method is introduced here that requires a single 3D acquisition, allowing good spatial coverage to be achieved in relatively short scan times.
METHODS: A multipathway multi-echo sequence was developed, and at least 3 pathways with 2 TEs were needed to generate T1 , T2 , T2 * , B1 + , and B0 maps. The method required the central k-space region to be sampled twice, with the same sequence but with 2 very different nominal flip angle settings. Consequently, scan time was only slightly longer than that of a single scan. The multipathway multi-echo data were reconstructed into parameter maps, for phantom as well as brain acquisitions, in 5 healthy volunteers at 3 T. Spatial resolution, matrix size, and FOV were 1.2 × 1.0 × 1.2 mm3 , 160 × 192 × 160, and 19.2 × 19.2 × 19.2 cm3 (whole brain), acquired in 11.5 minutes with minimal acceleration. Validation was performed against T1 , T2 , and T2 * maps calculated from gradient-echo and spin-echo data.
RESULTS: In Bland-Altman plots, bias and limits of agreement for T1 and T2 results in vivo and in phantom were -2.9/±125.5 ms (T1 in vivo), -4.8/±20.8 ms (T2 in vivo), -1.5/±18.1 ms (T1 in phantom), and -5.3/±7.4 ms (T2 in phantom), for regions of interest including given brain structures or phantom compartments. Due to relatively high noise levels, the current implementation of the approach may prove more useful for region of interest-based as opposed to pixel-based interpretation.
CONCLUSIONS: We proposed a novel approach to quantitatively map MR parameters based on a multipathway multi-echo acquisition.
© 2018 International Society for Magnetic Resonance in Medicine.

Entities:  

Keywords:  multipathway imaging; quantitative MRI; relaxometry

Mesh:

Year:  2018        PMID: 30320945      PMCID: PMC6347518          DOI: 10.1002/mrm.27525

Source DB:  PubMed          Journal:  Magn Reson Med        ISSN: 0740-3194            Impact factor:   4.668


  28 in total

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2.  Practical T2 quantitation for clinical applications.

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3.  Quantitative FLASH MRI at 3T using a rational approximation of the Ernst equation.

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5.  Triple echo steady-state (TESS) relaxometry.

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6.  A new steady-state imaging sequence for simultaneous acquisition of two MR images with clearly different contrasts.

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7.  Reversible, irreversible and effective transverse relaxation rates in normal aging brain at 3T.

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8.  Simultaneous variable flip angle-actual flip angle imaging method for improved accuracy and precision of three-dimensional T1 and B1 measurements.

Authors:  Samuel A Hurley; Vasily L Yarnykh; Kevin M Johnson; Aaron S Field; Andrew L Alexander; Alexey A Samsonov
Journal:  Magn Reson Med       Date:  2011-12-02       Impact factor: 4.668

9.  Quantitative mapping of T2 using partial spoiling.

Authors:  Oliver Bieri; Klaus Scheffler; Goetz H Welsch; S Trattnig; Tallal C Mamisch; Carl Ganter
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10.  Comparison of longitudinal metabolite relaxation times in different regions of the human brain at 1.5 and 3 Tesla.

Authors:  Thomas Ethofer; Irina Mader; Uwe Seeger; Gunther Helms; Michael Erb; Wolfgang Grodd; Albert Ludolph; Uwe Klose
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3.  Multi-pathway multi-echo acquisition and neural contrast translation to generate a variety of quantitative and qualitative image contrasts.

Authors:  Cheng-Chieh Cheng; Frank Preiswerk; Bruno Madore
Journal:  Magn Reson Med       Date:  2019-11-22       Impact factor: 4.668

4.  Feasibility of MR fingerprinting using a high-performance 0.55 T MRI system.

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