Cross-Communication Between Knee Osteoarthritis and Fibrosis: Molecular Pathways and Key Molecules.

IF 1.6 Q3 SPORT SCIENCES
Ioanna K Bolia, Kevin Mertz, Ethan Faye, Justin Sheppard, Sagar Telang, Jacob Bogdanov, Laith K Hasan, Aryan Haratian, Denis Evseenko, Alexander E Weber, Frank A Petrigliano
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引用次数: 3

Abstract

Knee fibrosis is characterized by the presence of excessive connective tissue due to dysregulated fibroblast activation following local or systemic tissue damage. Knee fibrosis constitutes a major clinical problem in orthopaedics due to the severe limitation in the knee range of motion that leads to compromised function and patient disability. Knee osteoarthritis is an extremely common orthopedic condition that is associated with patient disability and major costs to the health-care systems worldwide. Although knee fibrosis and osteoarthritis (OA) have traditionally been perceived as two separate pathologic entities, recent research has shown common ground between the pathophysiologic processes that lead to the development of these two conditions. The purpose of this review was to identify the pathophysiologic pathways as well as key molecules that are implicated in the development of both knee OA and knee fibrosis in order to understand the relationship between the two diagnoses and potentially identify novel therapeutic targets.

Abstract Image

Abstract Image

膝关节骨关节炎和纤维化之间的交叉交流:分子途径和关键分子。
膝关节纤维化的特点是由于局部或全身组织损伤后成纤维细胞激活失调而导致结缔组织过多。膝关节纤维化是骨科的一个主要临床问题,因为膝关节活动范围严重受限,导致功能受损和患者残疾。膝关节骨关节炎是一种极其常见的骨科疾病,与患者残疾和全球卫生保健系统的主要费用有关。虽然膝关节纤维化和骨关节炎(OA)传统上被认为是两种不同的病理实体,但最近的研究表明,导致这两种疾病发展的病理生理过程之间存在共同点。本综述的目的是确定与膝关节OA和膝关节纤维化发展相关的病理生理途径以及关键分子,以了解这两种诊断之间的关系,并潜在地确定新的治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
4.80
自引率
0.00%
发文量
13
审稿时长
16 weeks
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