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Uncovering associations between data-driven learned qMRI biomarkers and chronic pain

Knee pain is the most common and debilitating symptom of knee osteoarthritis (OA). While there is a perceived association between OA imaging biomarkers and pain, there are weak or conflicting findings for this relationship. This study uses Deep Learning (DL) models to elucidate associations between...

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Autores principales: Morales, Alejandro G., Lee, Jinhee J., Caliva, Francesco, Iriondo, Claudia, Liu, Felix, Majumdar, Sharmila, Pedoia, Valentina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8578418/
https://www.ncbi.nlm.nih.gov/pubmed/34753963
http://dx.doi.org/10.1038/s41598-021-01111-x
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author Morales, Alejandro G.
Lee, Jinhee J.
Caliva, Francesco
Iriondo, Claudia
Liu, Felix
Majumdar, Sharmila
Pedoia, Valentina
author_facet Morales, Alejandro G.
Lee, Jinhee J.
Caliva, Francesco
Iriondo, Claudia
Liu, Felix
Majumdar, Sharmila
Pedoia, Valentina
author_sort Morales, Alejandro G.
collection PubMed
description Knee pain is the most common and debilitating symptom of knee osteoarthritis (OA). While there is a perceived association between OA imaging biomarkers and pain, there are weak or conflicting findings for this relationship. This study uses Deep Learning (DL) models to elucidate associations between bone shape, cartilage thickness and T(2) relaxation times extracted from Magnetic Resonance Images (MRI) and chronic knee pain. Class Activation Maps (Grad-CAM) applied on the trained chronic pain DL models are used to evaluate the locations of features associated with presence and absence of pain. For the cartilage thickness biomarker, the presence of features sensitive for pain presence were generally located in the medial side, while the features specific for pain absence were generally located in the anterior lateral side. This suggests that the association of cartilage thickness and pain varies, requiring a more personalized averaging strategy. We propose a novel DL-guided definition for cartilage thickness spatial averaging based on Grad-CAM weights. We showed a significant improvement modeling chronic knee pain with the inclusion of the novel biomarker definition: likelihood ratio test p-values of 7.01 × 10(–33) and 1.93 × 10(–14) for DL-guided cartilage thickness averaging for the femur and tibia, respectively, compared to the cartilage thickness compartment averaging.
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spelling pubmed-85784182021-11-10 Uncovering associations between data-driven learned qMRI biomarkers and chronic pain Morales, Alejandro G. Lee, Jinhee J. Caliva, Francesco Iriondo, Claudia Liu, Felix Majumdar, Sharmila Pedoia, Valentina Sci Rep Article Knee pain is the most common and debilitating symptom of knee osteoarthritis (OA). While there is a perceived association between OA imaging biomarkers and pain, there are weak or conflicting findings for this relationship. This study uses Deep Learning (DL) models to elucidate associations between bone shape, cartilage thickness and T(2) relaxation times extracted from Magnetic Resonance Images (MRI) and chronic knee pain. Class Activation Maps (Grad-CAM) applied on the trained chronic pain DL models are used to evaluate the locations of features associated with presence and absence of pain. For the cartilage thickness biomarker, the presence of features sensitive for pain presence were generally located in the medial side, while the features specific for pain absence were generally located in the anterior lateral side. This suggests that the association of cartilage thickness and pain varies, requiring a more personalized averaging strategy. We propose a novel DL-guided definition for cartilage thickness spatial averaging based on Grad-CAM weights. We showed a significant improvement modeling chronic knee pain with the inclusion of the novel biomarker definition: likelihood ratio test p-values of 7.01 × 10(–33) and 1.93 × 10(–14) for DL-guided cartilage thickness averaging for the femur and tibia, respectively, compared to the cartilage thickness compartment averaging. Nature Publishing Group UK 2021-11-09 /pmc/articles/PMC8578418/ /pubmed/34753963 http://dx.doi.org/10.1038/s41598-021-01111-x Text en © The Author(s) 2021 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
Morales, Alejandro G.
Lee, Jinhee J.
Caliva, Francesco
Iriondo, Claudia
Liu, Felix
Majumdar, Sharmila
Pedoia, Valentina
Uncovering associations between data-driven learned qMRI biomarkers and chronic pain
title Uncovering associations between data-driven learned qMRI biomarkers and chronic pain
title_full Uncovering associations between data-driven learned qMRI biomarkers and chronic pain
title_fullStr Uncovering associations between data-driven learned qMRI biomarkers and chronic pain
title_full_unstemmed Uncovering associations between data-driven learned qMRI biomarkers and chronic pain
title_short Uncovering associations between data-driven learned qMRI biomarkers and chronic pain
title_sort uncovering associations between data-driven learned qmri biomarkers and chronic pain
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8578418/
https://www.ncbi.nlm.nih.gov/pubmed/34753963
http://dx.doi.org/10.1038/s41598-021-01111-x
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