决定创伤后疼痛和创伤后骨关节炎发展的因素

А.А. Черникова, А. Е. Каратеев, М.А. Макаров, Е.И. Бялик, С.А. Макаров, В.Е. Бялик, В.А. Нестеренко, Anastasia A. Chernikova, Andrey E. Karateev, Maxim A. Makarov, E. Bialik, Sergey A. Makarov, Valerii E. Bialik, V. Nesterenko, Polina E. Dudnikova
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摘要

损伤引起全身的神经、体液和行为反应,旨在恢复受损组织和纠正生物力学紊乱。然而,在许多情况下,完全修复是不可能的-创伤性损伤,炎症发生在其背景,退行性过程(纤维化,新生血管生成,异位骨化)导致严重的结构改变和功能能力的进行性下降。创伤最常见的并发症包括慢性创伤后疼痛和创伤后骨关节炎(pta)。这些并发症是相互关联的——10-50%的关节损伤患者会出现疼痛(伴有僵硬和功能障碍),这可能表明PTOA的早期(放射前)阶段的形成。典型的上睑下垂结构改变发生在膝关节损伤后10-15年(>30%的患者)。大关节的PTOA更具侵袭性,常伴有滑膜炎,需要关节置换术,平均比原发性骨关节炎早10-15年。PTOA的早期诊断是基于临床表现(主要是创伤后疼痛)的动态分析,关节结构早期变化的可视化(磁共振成像),以及炎症和骨软骨破坏生物标志物水平的研究。作为PTOA的其他危险因素,遗传特征被认为决定了炎症、疼痛和软骨和骨组织修复受损的慢性性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Factors determining the development of post-traumatic pain and post-traumatic osteoarthritis
Injuries cause a systemic neurohumoral and behavioral response of the body, aimed at restoring damaged tissues and correcting biomechanical disorders. However, in many cases, full-fledged repair is impossible – traumatic injury, inflammation that occurs against its background, and degenerative processes (fibrosis, neoangiogenesis, heterotopic ossification) lead to severe structural changes and a progressive decrease in functional ability. The most common complications of trauma include chronic post-traumatic pain and post-traumatic osteoarthritis (PTOA). These complications are interrelated – pain (accompanied by stiffness and dysfunction) that occurs in 10–50% of people who have suffered a joint injury may indicate the formation of early (pre-radiological) stages of PTOA. The development of typical structural changes in PTOA is observed 10–15 years after a knee injury (in >30% of patients). PTOA of large joints is more aggressive, often accompanied by synovitis, and requires arthroplasty on average 10–15 years earlier than primary osteoarthritis. Early diagnosis of PTOA is based on the analysis of the dynamics of clinical manifestations (primarily post-traumatic pain), visualization of early changes in the structure of the joint (magnetic resonance imaging), as well as the study of the level of biomarkers of inflammation and osteochondral destruction. As additional risk factors for PTOA, genetic features are considered that determine the chronicity of inflammation, pain, and impaired repair of cartilage and bone tissue.
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