Back to Search
Start Over
Assessment of higher-order singular value decomposition denoising methods on dynamic hyperpolarized [1- 13 C]pyruvate MRI data from patients with glioma.
- Source :
-
NeuroImage. Clinical [Neuroimage Clin] 2022; Vol. 36, pp. 103155. Date of Electronic Publication: 2022 Aug 17. - Publication Year :
- 2022
-
Abstract
- Background: Real-time metabolic conversion of intravenously-injected hyperpolarized [1- <superscript>13</superscript> C]pyruvate to [1- <superscript>13</superscript> C]lactate and [ <superscript>13</superscript> C]bicarbonate in the brain can be measured using dynamic hyperpolarized carbon-13 (HP- <superscript>13</superscript> C) MRI. However, voxel-wise evaluation of metabolism in patients with glioma is challenged by the limited signal-to-noise ratio (SNR) of downstream <superscript>13</superscript> C metabolites, especially within lesions. The purpose of this study was to evaluate the ability of higher-order singular value decomposition (HOSVD) denoising methods to enhance dynamic HP [1- <superscript>13</superscript> C]pyruvate MRI data acquired from patients with glioma.<br />Methods: Dynamic HP- <superscript>13</superscript> C MRI were acquired from 14 patients with glioma. The effects of two HOSVD denoising techniques, tensor rank truncation-image enhancement (TRI) and global-local HOSVD (GL-HOSVD), on the SNR and kinetic modeling were analyzed in [1- <superscript>13</superscript> C]lactate data with simulated noise that matched the levels of [ <superscript>13</superscript> C]bicarbonate signals. Both methods were then evaluated in patient data based on their ability to improve [1- <superscript>13</superscript> C]pyruvate, [1- <superscript>13</superscript> C]lactate and [ <superscript>13</superscript> C]bicarbonate SNR. The effects of denoising on voxel-wise kinetic modeling of k <subscript>PL</subscript> and k <subscript>PB</subscript> was also evaluated. The number of voxels with reliable kinetic modeling of pyruvate-to-lactate (k <subscript>PL</subscript> ) and pyruvate-to-bicarbonate (k <subscript>PB</subscript> ) conversion rates within regions of interest (ROIs) before and after denoising was then compared.<br />Results: Both denoising methods improved metabolite SNR and regional signal coverage. In patient data, the average increase in peak dynamic metabolite SNR was 2-fold using TRI and 4-5 folds using GL-HOSVD denoising compared to acquired data. Denoising reduced k <subscript>PL</subscript> modeling errors from a native average of 23% to 16% (TRI) and 15% (GL-HOSVD); and k <subscript>PB</subscript> error from 42% to 34% (TRI) and 37% (GL-HOSVD) (values were averaged voxelwise over all datasets). In contrast-enhancing lesions, the average number of voxels demonstrating within-tolerance k <subscript>PL</subscript> modeling error relative to the total voxels increased from 48% in the original data to 84% (TRI) and 90% (GL-HOSVD), while the number of voxels showing within-tolerance k <subscript>PB</subscript> modeling error increased from 0% to 15% (TRI) and 8% (GL-HOSVD).<br />Conclusion: Post-processing denoising methods significantly improved the SNR of dynamic HP- <superscript>13</superscript> C imaging data, resulting in a greater number of voxels satisfying minimum SNR criteria and maximum kinetic modeling errors in tumor lesions. This enhancement can aid in the voxel-wise analysis of HP- <superscript>13</superscript> C data and thereby improve monitoring of metabolic changes in patients with glioma following treatment.<br />Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2022 The Authors. Published by Elsevier Inc. All rights reserved.)
Details
- Language :
- English
- ISSN :
- 2213-1582
- Volume :
- 36
- Database :
- MEDLINE
- Journal :
- NeuroImage. Clinical
- Publication Type :
- Academic Journal
- Accession number :
- 36007439
- Full Text :
- https://doi.org/10.1016/j.nicl.2022.103155