Intraindividual Comparison of Compressed Sensing‐Accelerated Cartesian and Radial Arterial Phase Imaging of the Liver in an Experimental Tumor Model. Issue 7 (July 2021)
- Record Type:
- Journal Article
- Title:
- Intraindividual Comparison of Compressed Sensing‐Accelerated Cartesian and Radial Arterial Phase Imaging of the Liver in an Experimental Tumor Model. Issue 7 (July 2021)
- Main Title:
- Intraindividual Comparison of Compressed Sensing‐Accelerated Cartesian and Radial Arterial Phase Imaging of the Liver in an Experimental Tumor Model
- Authors:
- Harder, Felix N.
Budjan, Johannes
Nickel, Marcel D.
Grimm, Robert
Pietsch, Hubertus
Schoenberg, Stefan O.
Jost, Gregor
Attenberger, Ulrike I. - Abstract:
- Abstract : Objectives: The aim of this study was to intraindividually compare the performance of 2 compressed sensing (CS)‐accelerated magnetic resonance imaging (MRI) sequences, 1 featuring Cartesian (compressed sensing volumetric interpolated breath-hold examination [CS-VIBE]) and the other radial (golden-angle radial sparse parallel [GRASP]) k-space sampling in continuous dynamic imaging during hepatic vascular phases, using extracellular and hepatocyte-specific contrast agents. Materials and Methods: Seven New Zealand white rabbits, with induced VX2 liver tumors (median number of lesions, 2 ± 0.83; range, 1–3), received 2 continuously acquired T1-weighted prototype CS-accelerated MRI sequences (CS-VIBE and GRASP) with high spatial (0.8 × 0.8 × 1.5 mm) and temporal resolution (3.5 seconds) in randomized order on 2 separate days using a 1.5-T scanner. In all animals, imaging was performed using first gadobutrol at a dose of 0.1 mmol/kg and, then 45 minutes later, gadoxetic acid at a dose of 0.025 mmol/kg. The following qualitative parameters were assessed using 3- and 5-point Likert scales (3 and 5 being the highest scores respectively): image quality (IQ), arterial and venous vessel delineation, tumor enhancement, motion artifacts, and sequence-specific artifacts. Furthermore, the following quantitative parameters were obtained: relative peak signal enhancement, time to peak, mean transit time, and plasma flow ratios. Paired sampled t tests and Wilcoxon signed rank testsAbstract : Objectives: The aim of this study was to intraindividually compare the performance of 2 compressed sensing (CS)‐accelerated magnetic resonance imaging (MRI) sequences, 1 featuring Cartesian (compressed sensing volumetric interpolated breath-hold examination [CS-VIBE]) and the other radial (golden-angle radial sparse parallel [GRASP]) k-space sampling in continuous dynamic imaging during hepatic vascular phases, using extracellular and hepatocyte-specific contrast agents. Materials and Methods: Seven New Zealand white rabbits, with induced VX2 liver tumors (median number of lesions, 2 ± 0.83; range, 1–3), received 2 continuously acquired T1-weighted prototype CS-accelerated MRI sequences (CS-VIBE and GRASP) with high spatial (0.8 × 0.8 × 1.5 mm) and temporal resolution (3.5 seconds) in randomized order on 2 separate days using a 1.5-T scanner. In all animals, imaging was performed using first gadobutrol at a dose of 0.1 mmol/kg and, then 45 minutes later, gadoxetic acid at a dose of 0.025 mmol/kg. The following qualitative parameters were assessed using 3- and 5-point Likert scales (3 and 5 being the highest scores respectively): image quality (IQ), arterial and venous vessel delineation, tumor enhancement, motion artifacts, and sequence-specific artifacts. Furthermore, the following quantitative parameters were obtained: relative peak signal enhancement, time to peak, mean transit time, and plasma flow ratios. Paired sampled t tests and Wilcoxon signed rank tests were used for intraindividual comparison. Image analysis was performed by 2 radiologists. Results: Six of 7 animals underwent the full imaging protocol and obtained data were analyzed statistically. Overall IQ was rated moderate to excellent, not differing significantly between the 2 sequences. Gadobutrol-enhanced CS-VIBE examinations revealed the highest mean Likert scale values in terms of vessel delineation and tumor enhancement (arterial 4.4 [4–5], venous 4.3 [3–5], and tumor 2.9 [2–3]). Significantly, more sequence-specific artifacts were seen in GRASP examinations ( P = 0.008–0.031). However, these artifacts did not impair IQ. Excellent Likert scale ratings were found for motion artifacts in both sequences. In both sequences, a maximum of 4 hepatic arterial dominant phases were obtained. Regarding the relative peak signal enhancement, CS-VIBE and GRASP showed similar results. The relative peak signal enhancement values did not differ significantly between the 2 sequences in the aorta, the hepatic artery, or the inferior vena cava ( P = 0.063–0.536). However, significantly higher values were noted for CS-VIBE in gadoxetic acid–enhanced examinations in the portal vein ( P = 0.031) and regarding the tumor enhancement ( P = 0.005). Time to peak and mean transit time or plasma flow ratios did not differ significantly between the sequences. Conclusions: Both CS-VIBE and GRASP provide excellent results in dynamic liver MRI using extracellular and hepatocyte-specific contrast agents, in terms of IQ, peak signal intensity, and presence of artifacts. … (more)
- Is Part Of:
- Investigative radiology. Volume 56:Issue 7(2021)
- Journal:
- Investigative radiology
- Issue:
- Volume 56:Issue 7(2021)
- Issue Display:
- Volume 56, Issue 7 (2021)
- Year:
- 2021
- Volume:
- 56
- Issue:
- 7
- Issue Sort Value:
- 2021-0056-0007-0000
- Page Start:
- Page End:
- Publication Date:
- 2021-07
- Subjects:
- compressed sensing -- CS-VIBE -- GRASP -- gadobutrol -- gadoxetic acid -- DCE MRI -- liver MRI -- animal model
Diagnosis, Radioscopic -- Periodicals
Radiology, Medical -- Periodicals
616.0757 - Journal URLs:
- http://journals.lww.com/investigativeradiology/pages/default.aspx ↗
http://journals.lww.com ↗ - DOI:
- 10.1097/RLI.0000000000000767 ↗
- Languages:
- English
- ISSNs:
- 0020-9996
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4560.350000
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