Journal Article DKFZ-2025-02232

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In Vivo 3D Liver Imaging at 7 T Using kT-Point pTx Pulses and a 32-Tx-Channel Whole-Body Radiofrequency Coil Array.

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2025
Wiley New York, NY

NMR in biomedicine 38(12), e70170 () [10.1002/nbm.70170]
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Abstract: At 7 T, a main challenge is the flip angle variations arising from the spatially inhomogeneous B1 + transmit profiles of the RF coils. To address this problem, static pTx with local pTx body arrays has been used. However, for larger organs, such as the liver, local arrays provide insufficient homogeneity, and often dynamic pTx is needed. In this study, the benefits of a 32-Tx-channel remote array are shown. Relative channel-wise 3D B1 + maps are acquired in free breathing in 11:38 min with a radial phase encoding (RPE) acquisition scheme in five healthy volunteers at 7 T. For each subject, an ROI is drawn manually covering the whole liver. The necessary number of kT-point pTx pulses is analyzed by comparing L-curves that depict the tradeoff between FA homogeneity and RF power for a large range of regularization parameters. For all subjects, no FA dropouts remain, and CV values under 17% can be achieved with magnitude and phase shimming. Two to three kT-points showed a good tradeoff between FA homogeneity and RF power. To analyze different channel numbers, a fixed phase between the channel-wise B1 + maps is set to achieve 8, 16, or 20 B1 + maps for shimming. The higher channel number showed superior shimming performance for static and dynamic pTx. Comparing 32 versus 8 individual channels, a 1.3- to 1.6-fold improvement in homogeneity can be found for the same RF power using phase shimming. With 32 Tx channels, static pTx shim and two kT-points were applied in vivo in free breathing with a 3D RPE GRE sequence with 1.4-mm isotropic resolution. The in vivo signal magnitudes of the small FA acquisitions showed good agreement with the predicted relative B1 + maps while neglecting B0 nonuniformity. In summary, this study shows the advantages of using a remote 32-Tx channel array for in vivo liver imaging at 7 T.

Keyword(s): Humans (MeSH) ; Liver: diagnostic imaging (MeSH) ; Liver: anatomy & histology (MeSH) ; Imaging, Three-Dimensional: instrumentation (MeSH) ; Imaging, Three-Dimensional: methods (MeSH) ; Adult (MeSH) ; Male (MeSH) ; Radio Waves (MeSH) ; Female (MeSH) ; Magnetic Resonance Imaging: instrumentation (MeSH) ; Magnetic Resonance Imaging: methods (MeSH) ; Whole Body Imaging: instrumentation (MeSH) ; Young Adult (MeSH)

Classification:

Note: #EA:E020#LA:E020#

Contributing Institute(s):
  1. E020 Med. Physik in der Radiologie (E020)
Research Program(s):
  1. 315 - Bildgebung und Radioonkologie (POF4-315) (POF4-315)

Appears in the scientific report 2025
Database coverage:
Medline ; OpenAccess ; Clarivate Analytics Master Journal List ; Current Contents - Life Sciences ; DEAL Wiley ; Essential Science Indicators ; IF < 5 ; JCR ; NationallizenzNationallizenz ; SCOPUS ; Science Citation Index Expanded ; Web of Science Core Collection
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 Record created 2025-10-30, last modified 2026-04-15


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