Cargando…
A serial multiparametric quantitative magnetic resonance imaging study to assess proteoglycan depletion of human articular cartilage and its effects on functionality
Water, collagen, and proteoglycans determine articular cartilage functionality. If altered, susceptibility to premature degeneration is increased. This study investigated the effects of enzymatic proteoglycan depletion on cartilage functionality as assessed by advanced Magnetic Resonance Imaging (MR...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7492285/ https://www.ncbi.nlm.nih.gov/pubmed/32934341 http://dx.doi.org/10.1038/s41598-020-72208-y |
_version_ | 1783582359375839232 |
---|---|
author | Hafner, Tobias Schock, Justus Post, Manuel Abrar, Daniel Benjamin Sewerin, Philipp Linka, Kevin Knobe, Matthias Kuhl, Christiane Truhn, Daniel Nebelung, Sven |
author_facet | Hafner, Tobias Schock, Justus Post, Manuel Abrar, Daniel Benjamin Sewerin, Philipp Linka, Kevin Knobe, Matthias Kuhl, Christiane Truhn, Daniel Nebelung, Sven |
author_sort | Hafner, Tobias |
collection | PubMed |
description | Water, collagen, and proteoglycans determine articular cartilage functionality. If altered, susceptibility to premature degeneration is increased. This study investigated the effects of enzymatic proteoglycan depletion on cartilage functionality as assessed by advanced Magnetic Resonance Imaging (MRI) techniques under standardized loading. Lateral femoral condylar cartilage-bone samples from patients undergoing knee replacement (n = 29) were serially imaged by Proton Density-weighted and T1, T1ρ, T2, and T2* mapping sequences on a clinical 3.0 T MRI scanner (Achieva, Philips). Using pressure-controlled indentation loading, samples were imaged unloaded and quasi-statically loaded to 15.1 N and 28.6 N, and both before and after exposure to low-concentrated (LT, 0.1 mg/mL, n = 10) or high-concentrated trypsin (HT, 1.0 mg/mL, n = 10). Controls were not treated (n = 9). Responses to loading were assessed for the entire sample and regionally, i.e. sub- and peri-pistonally, and zonally, i.e. upper and lower sample halves. Trypsin effects were quantified as relative changes (Δ), analysed using appropriate statistical tests, and referenced histologically. Histological proteoglycan depletion was reflected by significant sub-pistonal decreases in T1 (p = 0.003) and T2 (p = 0.008) after HT exposure. Loading-induced changes in T1ρ and T2* were not related. In conclusion, proteoglycan depletion alters cartilage functionality and may be assessed using serial T1 and T2 mapping under loading. |
format | Online Article Text |
id | pubmed-7492285 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-74922852020-09-16 A serial multiparametric quantitative magnetic resonance imaging study to assess proteoglycan depletion of human articular cartilage and its effects on functionality Hafner, Tobias Schock, Justus Post, Manuel Abrar, Daniel Benjamin Sewerin, Philipp Linka, Kevin Knobe, Matthias Kuhl, Christiane Truhn, Daniel Nebelung, Sven Sci Rep Article Water, collagen, and proteoglycans determine articular cartilage functionality. If altered, susceptibility to premature degeneration is increased. This study investigated the effects of enzymatic proteoglycan depletion on cartilage functionality as assessed by advanced Magnetic Resonance Imaging (MRI) techniques under standardized loading. Lateral femoral condylar cartilage-bone samples from patients undergoing knee replacement (n = 29) were serially imaged by Proton Density-weighted and T1, T1ρ, T2, and T2* mapping sequences on a clinical 3.0 T MRI scanner (Achieva, Philips). Using pressure-controlled indentation loading, samples were imaged unloaded and quasi-statically loaded to 15.1 N and 28.6 N, and both before and after exposure to low-concentrated (LT, 0.1 mg/mL, n = 10) or high-concentrated trypsin (HT, 1.0 mg/mL, n = 10). Controls were not treated (n = 9). Responses to loading were assessed for the entire sample and regionally, i.e. sub- and peri-pistonally, and zonally, i.e. upper and lower sample halves. Trypsin effects were quantified as relative changes (Δ), analysed using appropriate statistical tests, and referenced histologically. Histological proteoglycan depletion was reflected by significant sub-pistonal decreases in T1 (p = 0.003) and T2 (p = 0.008) after HT exposure. Loading-induced changes in T1ρ and T2* were not related. In conclusion, proteoglycan depletion alters cartilage functionality and may be assessed using serial T1 and T2 mapping under loading. Nature Publishing Group UK 2020-09-15 /pmc/articles/PMC7492285/ /pubmed/32934341 http://dx.doi.org/10.1038/s41598-020-72208-y Text en © The Author(s) 2020 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/. |
spellingShingle | Article Hafner, Tobias Schock, Justus Post, Manuel Abrar, Daniel Benjamin Sewerin, Philipp Linka, Kevin Knobe, Matthias Kuhl, Christiane Truhn, Daniel Nebelung, Sven A serial multiparametric quantitative magnetic resonance imaging study to assess proteoglycan depletion of human articular cartilage and its effects on functionality |
title | A serial multiparametric quantitative magnetic resonance imaging study to assess proteoglycan depletion of human articular cartilage and its effects on functionality |
title_full | A serial multiparametric quantitative magnetic resonance imaging study to assess proteoglycan depletion of human articular cartilage and its effects on functionality |
title_fullStr | A serial multiparametric quantitative magnetic resonance imaging study to assess proteoglycan depletion of human articular cartilage and its effects on functionality |
title_full_unstemmed | A serial multiparametric quantitative magnetic resonance imaging study to assess proteoglycan depletion of human articular cartilage and its effects on functionality |
title_short | A serial multiparametric quantitative magnetic resonance imaging study to assess proteoglycan depletion of human articular cartilage and its effects on functionality |
title_sort | serial multiparametric quantitative magnetic resonance imaging study to assess proteoglycan depletion of human articular cartilage and its effects on functionality |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7492285/ https://www.ncbi.nlm.nih.gov/pubmed/32934341 http://dx.doi.org/10.1038/s41598-020-72208-y |
work_keys_str_mv | AT hafnertobias aserialmultiparametricquantitativemagneticresonanceimagingstudytoassessproteoglycandepletionofhumanarticularcartilageanditseffectsonfunctionality AT schockjustus aserialmultiparametricquantitativemagneticresonanceimagingstudytoassessproteoglycandepletionofhumanarticularcartilageanditseffectsonfunctionality AT postmanuel aserialmultiparametricquantitativemagneticresonanceimagingstudytoassessproteoglycandepletionofhumanarticularcartilageanditseffectsonfunctionality AT abrardanielbenjamin aserialmultiparametricquantitativemagneticresonanceimagingstudytoassessproteoglycandepletionofhumanarticularcartilageanditseffectsonfunctionality AT sewerinphilipp aserialmultiparametricquantitativemagneticresonanceimagingstudytoassessproteoglycandepletionofhumanarticularcartilageanditseffectsonfunctionality AT linkakevin aserialmultiparametricquantitativemagneticresonanceimagingstudytoassessproteoglycandepletionofhumanarticularcartilageanditseffectsonfunctionality AT knobematthias aserialmultiparametricquantitativemagneticresonanceimagingstudytoassessproteoglycandepletionofhumanarticularcartilageanditseffectsonfunctionality AT kuhlchristiane aserialmultiparametricquantitativemagneticresonanceimagingstudytoassessproteoglycandepletionofhumanarticularcartilageanditseffectsonfunctionality AT truhndaniel aserialmultiparametricquantitativemagneticresonanceimagingstudytoassessproteoglycandepletionofhumanarticularcartilageanditseffectsonfunctionality AT nebelungsven aserialmultiparametricquantitativemagneticresonanceimagingstudytoassessproteoglycandepletionofhumanarticularcartilageanditseffectsonfunctionality AT hafnertobias serialmultiparametricquantitativemagneticresonanceimagingstudytoassessproteoglycandepletionofhumanarticularcartilageanditseffectsonfunctionality AT schockjustus serialmultiparametricquantitativemagneticresonanceimagingstudytoassessproteoglycandepletionofhumanarticularcartilageanditseffectsonfunctionality AT postmanuel serialmultiparametricquantitativemagneticresonanceimagingstudytoassessproteoglycandepletionofhumanarticularcartilageanditseffectsonfunctionality AT abrardanielbenjamin serialmultiparametricquantitativemagneticresonanceimagingstudytoassessproteoglycandepletionofhumanarticularcartilageanditseffectsonfunctionality AT sewerinphilipp serialmultiparametricquantitativemagneticresonanceimagingstudytoassessproteoglycandepletionofhumanarticularcartilageanditseffectsonfunctionality AT linkakevin serialmultiparametricquantitativemagneticresonanceimagingstudytoassessproteoglycandepletionofhumanarticularcartilageanditseffectsonfunctionality AT knobematthias serialmultiparametricquantitativemagneticresonanceimagingstudytoassessproteoglycandepletionofhumanarticularcartilageanditseffectsonfunctionality AT kuhlchristiane serialmultiparametricquantitativemagneticresonanceimagingstudytoassessproteoglycandepletionofhumanarticularcartilageanditseffectsonfunctionality AT truhndaniel serialmultiparametricquantitativemagneticresonanceimagingstudytoassessproteoglycandepletionofhumanarticularcartilageanditseffectsonfunctionality AT nebelungsven serialmultiparametricquantitativemagneticresonanceimagingstudytoassessproteoglycandepletionofhumanarticularcartilageanditseffectsonfunctionality |