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Multicomponent analysis of T(1) relaxation in bovine articular cartilage at low magnetic fields
PURPOSE: The multi‐exponential character of T(1) relaxation in bovine articular cartilage was investigated at low magnetic fields below 0.5 T. The ultimate aim was to identify a parameter based on the T(1) relaxation time distribution as a biomarker to biochemical features of osteoarthritis. METHODS...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6718012/ https://www.ncbi.nlm.nih.gov/pubmed/30537283 http://dx.doi.org/10.1002/mrm.27624 |
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author | Petrov, Oleg V. Stapf, Siegfried |
author_facet | Petrov, Oleg V. Stapf, Siegfried |
author_sort | Petrov, Oleg V. |
collection | PubMed |
description | PURPOSE: The multi‐exponential character of T(1) relaxation in bovine articular cartilage was investigated at low magnetic fields below 0.5 T. The ultimate aim was to identify a parameter based on the T(1) relaxation time distribution as a biomarker to biochemical features of osteoarthritis. METHODS: Osteoarthritis conditions were simulated by enzymatic digestion of cartilage with trypsin. Fast‐field cycling NMR relaxometry was carried out in the magnetic field range B(0) = 70 μT to 600 mT. The data were analyzed in terms of T(1) distributions on a log‐time scale using inverse Laplace transform, whereas integral properties such as mean T(1)s and distribution widths were obtained without data inversion from logarithmic moment analysis and a stretched‐exponential fit to the data. Attempts were also made to differentiate between water dynamic components through multi‐Lorentzian decomposition of average relaxation‐rate dispersions. RESULTS: T(1) distribution in bovine articular cartilage was found to be bimodal, with the dominating, long component shifting toward larger values following trypsin digestion. The effect is more prominent toward lower magnetic field strength. This shift leads to an overall increase of the distribution width and an equivalently more pronounced deviation from exponential behavior. CONCLUSION: The logarithmic width of T(1) distribution functions at fields of 0.5 T and below, and the stretched‐exponential decay fit exponent β, show a significant trend after trypsin digestion of cartilage. These 2 parameters are suggested as possible biomarkers for osteoarthritis in humans and can be acquired entirely in vivo, with increasing significance for lower magnetic field strengths. |
format | Online Article Text |
id | pubmed-6718012 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-67180122019-09-06 Multicomponent analysis of T(1) relaxation in bovine articular cartilage at low magnetic fields Petrov, Oleg V. Stapf, Siegfried Magn Reson Med Full Papers—Spectroscopic Methodology PURPOSE: The multi‐exponential character of T(1) relaxation in bovine articular cartilage was investigated at low magnetic fields below 0.5 T. The ultimate aim was to identify a parameter based on the T(1) relaxation time distribution as a biomarker to biochemical features of osteoarthritis. METHODS: Osteoarthritis conditions were simulated by enzymatic digestion of cartilage with trypsin. Fast‐field cycling NMR relaxometry was carried out in the magnetic field range B(0) = 70 μT to 600 mT. The data were analyzed in terms of T(1) distributions on a log‐time scale using inverse Laplace transform, whereas integral properties such as mean T(1)s and distribution widths were obtained without data inversion from logarithmic moment analysis and a stretched‐exponential fit to the data. Attempts were also made to differentiate between water dynamic components through multi‐Lorentzian decomposition of average relaxation‐rate dispersions. RESULTS: T(1) distribution in bovine articular cartilage was found to be bimodal, with the dominating, long component shifting toward larger values following trypsin digestion. The effect is more prominent toward lower magnetic field strength. This shift leads to an overall increase of the distribution width and an equivalently more pronounced deviation from exponential behavior. CONCLUSION: The logarithmic width of T(1) distribution functions at fields of 0.5 T and below, and the stretched‐exponential decay fit exponent β, show a significant trend after trypsin digestion of cartilage. These 2 parameters are suggested as possible biomarkers for osteoarthritis in humans and can be acquired entirely in vivo, with increasing significance for lower magnetic field strengths. John Wiley and Sons Inc. 2018-12-10 2019-05 /pmc/articles/PMC6718012/ /pubmed/30537283 http://dx.doi.org/10.1002/mrm.27624 Text en © 2018 The Authors Magnetic Resonance in Medicine published by Wiley Periodicals, Inc. on behalf of International Society for Magnetic Resonance in Medicine This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Full Papers—Spectroscopic Methodology Petrov, Oleg V. Stapf, Siegfried Multicomponent analysis of T(1) relaxation in bovine articular cartilage at low magnetic fields |
title | Multicomponent analysis of T(1) relaxation in bovine articular cartilage at low magnetic fields |
title_full | Multicomponent analysis of T(1) relaxation in bovine articular cartilage at low magnetic fields |
title_fullStr | Multicomponent analysis of T(1) relaxation in bovine articular cartilage at low magnetic fields |
title_full_unstemmed | Multicomponent analysis of T(1) relaxation in bovine articular cartilage at low magnetic fields |
title_short | Multicomponent analysis of T(1) relaxation in bovine articular cartilage at low magnetic fields |
title_sort | multicomponent analysis of t(1) relaxation in bovine articular cartilage at low magnetic fields |
topic | Full Papers—Spectroscopic Methodology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6718012/ https://www.ncbi.nlm.nih.gov/pubmed/30537283 http://dx.doi.org/10.1002/mrm.27624 |
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