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ACR Open Rheumatol. 2024 Apr;6(4):205-213. doi: 10.1002/acr2.11610. Epub 2024 Feb 4.
2
Mocetinostat activates Krüppel-like factor 4 and protects against tissue destruction and inflammation in osteoarthritis.莫塞替尼激活 Kruppel 样因子 4,可防止骨关节炎中的组织破坏和炎症。
JCI Insight. 2023 Sep 8;8(17):e170513. doi: 10.1172/jci.insight.170513.
3
Evaluation of S201086/GLPG1972, an ADAMTS-5 inhibitor, for the treatment of knee osteoarthritis in ROCCELLA: a phase 2 randomized clinical trial.评价 S201086/GLPG1972,一种 ADAMTS-5 抑制剂,用于治疗 ROCCELLA 中的膝骨关节炎:一项 2 期随机临床试验。
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Disease-modifying therapeutic strategies in osteoarthritis: current status and future directions.骨关节炎的疾病修饰治疗策略:现状与未来方向。
Exp Mol Med. 2021 Nov;53(11):1689-1696. doi: 10.1038/s12276-021-00710-y. Epub 2021 Nov 30.

骨关节炎当前治疗选择的简要综述,包括改善病情的骨关节炎药物(DMOADs)和新型疗法。

A brief review of current treatment options for osteoarthritis including disease-modifying osteoarthritis drugs (DMOADs) and novel therapeutics.

作者信息

Jiang Peng, Hu Kan, Jin Liang, Luo Zhicheng

机构信息

The Second Affiliated Hospital Zhejiang University School of Medicine Changxing Campus, Taihu Middle Road, Changxing County, Zhejiang Province, China.

出版信息

Ann Med Surg (Lond). 2024 Jun 4;86(7):4042-4048. doi: 10.1097/MS9.0000000000002214. eCollection 2024 Jul.

DOI:10.1097/MS9.0000000000002214
PMID:38989236
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11230824/
Abstract

Osteoarthritis (OA) is a chronic disorder caused by degenerative changes in articular cartilage, which are mainly manifests as degeneration of cartilage, subchondral bone remodeling, as well as synovial inflammation. Over the next few decades, OA and its burden will continue to increase worldwide, posing a major public health challenge for the foreseeable future. Treatment for OA includes non-pharmacological, pharmacological, and surgical treatments. Existing conservative treatments and joint surgery can only alleviate the symptoms and cannot be cured, so new therapies for OA are urgently needed. Since advances in the understanding of OA pathophysiology, researchers have identified some potential therapeutic targets against degeneration of cartilage, subchondral bone remodeling and synovial inflammation, enabling development of the disease-modifying OA drugs (DMOADs). Additionally, a number of new technologies are also being investigated for treating OA, such as RNA interference (RNAi), CRISPR/Cas9 and PROTAC. The goal of this review is to describe the current development status of DMOADs and to discuss the potential of emerging therapeutic approaches for treating OA, thus providing a reference for OA treatments.

摘要

骨关节炎(OA)是一种由关节软骨退行性变引起的慢性疾病,主要表现为软骨退变、软骨下骨重塑以及滑膜炎症。在未来几十年里,OA及其负担在全球范围内将持续增加,在可预见的未来构成一项重大的公共卫生挑战。OA的治疗包括非药物治疗、药物治疗和手术治疗。现有的保守治疗和关节手术只能缓解症状,无法治愈,因此迫切需要针对OA的新疗法。自从对OA病理生理学的认识取得进展以来,研究人员已经确定了一些针对软骨退变、软骨下骨重塑和滑膜炎症的潜在治疗靶点,从而能够开发改善病情的OA药物(DMOADs)。此外,一些新技术也正在被研究用于治疗OA,如RNA干扰(RNAi)、CRISPR/Cas9和PROTAC。本综述的目的是描述DMOADs的当前发展状况,并讨论新兴治疗方法治疗OA的潜力,从而为OA治疗提供参考。