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Optimization of spin-lock times for T(1ρ) mapping of human knee cartilage with bi- and stretched-exponential models

Two optimization criteria based on Cramér-Rao Bounds are compared between each other and with non-optimized schedules for T(1ρ) mapping using synthetic data, model phantoms, and in-vivo knee cartilage. The curve fitting is done on complex-valued data using an iterative Nonlinear Least Squares (NLS)...

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Autores principales: de Moura, Hector L., Menon, Rajiv G., Zibetti, Marcelo V. W., Regatte, Ravinder R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9546896/
https://www.ncbi.nlm.nih.gov/pubmed/36207361
http://dx.doi.org/10.1038/s41598-022-21269-2
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author de Moura, Hector L.
Menon, Rajiv G.
Zibetti, Marcelo V. W.
Regatte, Ravinder R.
author_facet de Moura, Hector L.
Menon, Rajiv G.
Zibetti, Marcelo V. W.
Regatte, Ravinder R.
author_sort de Moura, Hector L.
collection PubMed
description Two optimization criteria based on Cramér-Rao Bounds are compared between each other and with non-optimized schedules for T(1ρ) mapping using synthetic data, model phantoms, and in-vivo knee cartilage. The curve fitting is done on complex-valued data using an iterative Nonlinear Least Squares (NLS) approach. The optimization criteria are compared based on the Mean Normalized Absolute Error (MNAE) and variance of the estimated parameters. The optimized spin-lock time (TSL) schedules provided improved results over the non-optimized schedules for all cases that were tested. The simulations showed that optimized schedules can reach the same precision and reduce acquisition times by 16.5 min (42%) for the bi-exponential model, and 6.6 min (22%) for the stretched-exponential model. In the model phantoms experiments, the bi-exponential MNAE was reduced from 0.47 to 0.36, while stretched-exponential from 0.28 to 0.20 with a Modified Cramér-Rao Lower Bound (MCRLB). In-vivo knee cartilage experiments show a reduction in bi-exponential MNAE from 0.47 to 0.31, and stretched-exponential from 0.047 to 0.039. The optimized spin-lock times criteria reduced the error in all cases, being more significant in the synthetic data and model phantoms. The optimized TSL schedules can be either used to improve the quality of parameter maps or reduce scan time.
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spelling pubmed-95468962022-10-09 Optimization of spin-lock times for T(1ρ) mapping of human knee cartilage with bi- and stretched-exponential models de Moura, Hector L. Menon, Rajiv G. Zibetti, Marcelo V. W. Regatte, Ravinder R. Sci Rep Article Two optimization criteria based on Cramér-Rao Bounds are compared between each other and with non-optimized schedules for T(1ρ) mapping using synthetic data, model phantoms, and in-vivo knee cartilage. The curve fitting is done on complex-valued data using an iterative Nonlinear Least Squares (NLS) approach. The optimization criteria are compared based on the Mean Normalized Absolute Error (MNAE) and variance of the estimated parameters. The optimized spin-lock time (TSL) schedules provided improved results over the non-optimized schedules for all cases that were tested. The simulations showed that optimized schedules can reach the same precision and reduce acquisition times by 16.5 min (42%) for the bi-exponential model, and 6.6 min (22%) for the stretched-exponential model. In the model phantoms experiments, the bi-exponential MNAE was reduced from 0.47 to 0.36, while stretched-exponential from 0.28 to 0.20 with a Modified Cramér-Rao Lower Bound (MCRLB). In-vivo knee cartilage experiments show a reduction in bi-exponential MNAE from 0.47 to 0.31, and stretched-exponential from 0.047 to 0.039. The optimized spin-lock times criteria reduced the error in all cases, being more significant in the synthetic data and model phantoms. The optimized TSL schedules can be either used to improve the quality of parameter maps or reduce scan time. Nature Publishing Group UK 2022-10-07 /pmc/articles/PMC9546896/ /pubmed/36207361 http://dx.doi.org/10.1038/s41598-022-21269-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
de Moura, Hector L.
Menon, Rajiv G.
Zibetti, Marcelo V. W.
Regatte, Ravinder R.
Optimization of spin-lock times for T(1ρ) mapping of human knee cartilage with bi- and stretched-exponential models
title Optimization of spin-lock times for T(1ρ) mapping of human knee cartilage with bi- and stretched-exponential models
title_full Optimization of spin-lock times for T(1ρ) mapping of human knee cartilage with bi- and stretched-exponential models
title_fullStr Optimization of spin-lock times for T(1ρ) mapping of human knee cartilage with bi- and stretched-exponential models
title_full_unstemmed Optimization of spin-lock times for T(1ρ) mapping of human knee cartilage with bi- and stretched-exponential models
title_short Optimization of spin-lock times for T(1ρ) mapping of human knee cartilage with bi- and stretched-exponential models
title_sort optimization of spin-lock times for t(1ρ) mapping of human knee cartilage with bi- and stretched-exponential models
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9546896/
https://www.ncbi.nlm.nih.gov/pubmed/36207361
http://dx.doi.org/10.1038/s41598-022-21269-2
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