Cargando…
Bone marrow lesions in osteoarthritis: From basic science to clinical implications
Osteoarthritis (OA) is the most prevalent musculoskeletal disease characterized by multiple joint structure damages, including articular cartilage, subchondral bone and synovium, resulting in disability and economic burden. Bone marrow lesions (BMLs) are common and important magnetic resonance imagi...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9996250/ https://www.ncbi.nlm.nih.gov/pubmed/36909666 http://dx.doi.org/10.1016/j.bonr.2023.101667 |
_version_ | 1784903000933793792 |
---|---|
author | Shi, Xiaorui Mai, Yiying Fang, Xiaofeng Wang, Zhiqiang Xue, Song Chen, Haowei Dang, Qin Wang, Xiaoshuai Tang, Su'an Ding, Changhai Zhu, Zhaohua |
author_facet | Shi, Xiaorui Mai, Yiying Fang, Xiaofeng Wang, Zhiqiang Xue, Song Chen, Haowei Dang, Qin Wang, Xiaoshuai Tang, Su'an Ding, Changhai Zhu, Zhaohua |
author_sort | Shi, Xiaorui |
collection | PubMed |
description | Osteoarthritis (OA) is the most prevalent musculoskeletal disease characterized by multiple joint structure damages, including articular cartilage, subchondral bone and synovium, resulting in disability and economic burden. Bone marrow lesions (BMLs) are common and important magnetic resonance imaging (MRI) features in OA patients. Basic and clinical research on subchondral BMLs in the pathogenesis of OA has been a hotspot. New evidence shows that subchondral bone degeneration, including BML and angiogenesis, occurs not only at or after cartilage degeneration, but even earlier than cartilage degeneration. Although BMLs are recognized as important biomarkers for OA, their exact roles in the pathogenesis of OA are still unclear, and disputes about the clinical impact and treatment of BMLs remain. This review summarizes the current basic and clinical research progress of BMLs. We particularly focus on molecular pathways, cellular abnormalities and microenvironmental changes of subchondral bone that contributed to the formation of BMLs, and emphasize the crosstalk between subchondral bone and cartilage in OA development. Finally, potential therapeutic strategies targeting BMLs in OA are discussed, which provides novel strategies for OA treatment. |
format | Online Article Text |
id | pubmed-9996250 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-99962502023-03-10 Bone marrow lesions in osteoarthritis: From basic science to clinical implications Shi, Xiaorui Mai, Yiying Fang, Xiaofeng Wang, Zhiqiang Xue, Song Chen, Haowei Dang, Qin Wang, Xiaoshuai Tang, Su'an Ding, Changhai Zhu, Zhaohua Bone Rep Articles from the Special Issue on "Cartilage and bone crosstalk in development, homeostasis, aging, and diseases", Edited by Frank Beier and Ling Qin Osteoarthritis (OA) is the most prevalent musculoskeletal disease characterized by multiple joint structure damages, including articular cartilage, subchondral bone and synovium, resulting in disability and economic burden. Bone marrow lesions (BMLs) are common and important magnetic resonance imaging (MRI) features in OA patients. Basic and clinical research on subchondral BMLs in the pathogenesis of OA has been a hotspot. New evidence shows that subchondral bone degeneration, including BML and angiogenesis, occurs not only at or after cartilage degeneration, but even earlier than cartilage degeneration. Although BMLs are recognized as important biomarkers for OA, their exact roles in the pathogenesis of OA are still unclear, and disputes about the clinical impact and treatment of BMLs remain. This review summarizes the current basic and clinical research progress of BMLs. We particularly focus on molecular pathways, cellular abnormalities and microenvironmental changes of subchondral bone that contributed to the formation of BMLs, and emphasize the crosstalk between subchondral bone and cartilage in OA development. Finally, potential therapeutic strategies targeting BMLs in OA are discussed, which provides novel strategies for OA treatment. Elsevier 2023-02-25 /pmc/articles/PMC9996250/ /pubmed/36909666 http://dx.doi.org/10.1016/j.bonr.2023.101667 Text en © 2023 The Authors. Published by Elsevier Inc. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Articles from the Special Issue on "Cartilage and bone crosstalk in development, homeostasis, aging, and diseases", Edited by Frank Beier and Ling Qin Shi, Xiaorui Mai, Yiying Fang, Xiaofeng Wang, Zhiqiang Xue, Song Chen, Haowei Dang, Qin Wang, Xiaoshuai Tang, Su'an Ding, Changhai Zhu, Zhaohua Bone marrow lesions in osteoarthritis: From basic science to clinical implications |
title | Bone marrow lesions in osteoarthritis: From basic science to clinical implications |
title_full | Bone marrow lesions in osteoarthritis: From basic science to clinical implications |
title_fullStr | Bone marrow lesions in osteoarthritis: From basic science to clinical implications |
title_full_unstemmed | Bone marrow lesions in osteoarthritis: From basic science to clinical implications |
title_short | Bone marrow lesions in osteoarthritis: From basic science to clinical implications |
title_sort | bone marrow lesions in osteoarthritis: from basic science to clinical implications |
topic | Articles from the Special Issue on "Cartilage and bone crosstalk in development, homeostasis, aging, and diseases", Edited by Frank Beier and Ling Qin |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9996250/ https://www.ncbi.nlm.nih.gov/pubmed/36909666 http://dx.doi.org/10.1016/j.bonr.2023.101667 |
work_keys_str_mv | AT shixiaorui bonemarrowlesionsinosteoarthritisfrombasicsciencetoclinicalimplications AT maiyiying bonemarrowlesionsinosteoarthritisfrombasicsciencetoclinicalimplications AT fangxiaofeng bonemarrowlesionsinosteoarthritisfrombasicsciencetoclinicalimplications AT wangzhiqiang bonemarrowlesionsinosteoarthritisfrombasicsciencetoclinicalimplications AT xuesong bonemarrowlesionsinosteoarthritisfrombasicsciencetoclinicalimplications AT chenhaowei bonemarrowlesionsinosteoarthritisfrombasicsciencetoclinicalimplications AT dangqin bonemarrowlesionsinosteoarthritisfrombasicsciencetoclinicalimplications AT wangxiaoshuai bonemarrowlesionsinosteoarthritisfrombasicsciencetoclinicalimplications AT tangsuan bonemarrowlesionsinosteoarthritisfrombasicsciencetoclinicalimplications AT dingchanghai bonemarrowlesionsinosteoarthritisfrombasicsciencetoclinicalimplications AT zhuzhaohua bonemarrowlesionsinosteoarthritisfrombasicsciencetoclinicalimplications |