Division of Rheumatology, Allergy & Immunology, Tufts Medical Center, 800 Washington Street, Box #406, Boston, MA, 02111, USA.
Department of Quantitative Health Sciences, University of Massachusetts Medical School, Worcester, MA, USA.
BMC Musculoskelet Disord. 2020 May 29;21(1):332. doi: 10.1186/s12891-020-03367-2.
BACKGROUND: Osteoarthritis is generally a slowly progressive disorder. However, at least 1 in 7 people with incident knee osteoarthritis develop an abrupt progression to advanced-stage radiographic disease, many within 12 months. We summarize what is known - primarily based on findings from the Osteoarthritis Initiative - about the risk factors and natural history of accelerated knee osteoarthritis (AKOA) - defined as a transition from no radiographic knee osteoarthritis to advanced-stage disease < 4 years - and put these findings in context with typical osteoarthritis (slowly progressing disease), aging, prior case reports/series, and relevant animal models. Risk factors in the 2 to 4 years before radiographic manifestation of AKOA (onset) include older age, higher body mass index, altered joint alignment, contralateral osteoarthritis, greater pre-radiographic disease burden (structural, symptoms, and function), or low fasting glucose. One to 2 years before AKOA onset people often exhibit rapid articular cartilage loss, larger bone marrow lesions and effusion-synovitis, more meniscal pathology, slower chair-stand or walking pace, and increased global impact of arthritis than adults with typical knee osteoarthritis. Increased joint symptoms predispose a person to new joint trauma, which for someone who develops AKOA is often characterized by a destabilizing meniscal tear (e.g., radial or root tear). One in 7 people with AKOA onset subsequently receive a knee replacement during a 9-year period. The median time from any increase in radiographic severity to knee replacement is only 2.3 years. Despite some similarities, AKOA is different than other rapidly progressive arthropathies and collapsing these phenomena together or extracting results from one type of osteoarthritis to another should be avoided until further research comparing these types of osteoarthritis is conducted. Animal models that induce meniscal damage in the presence of other risk factors or create an incongruent distribution of loading on joints create an accelerated form of osteoarthritis compared to other models and may offer insights into AKOA. CONCLUSION: Accelerated knee osteoarthritis is unique from typical knee osteoarthritis. The incidence of AKOA in the Osteoarthritis Initiative and Chingford Study is substantial. AKOA needs to be taken into account and studied in epidemiologic studies and clinical trials.
背景:骨关节炎通常是一种缓慢进展的疾病。然而,至少有 1/7 的新发膝关节骨关节炎患者会出现影像学疾病的急剧进展,其中许多患者在 12 个月内进展为晚期。我们总结了目前已知的关于加速性膝关节骨关节炎(AKOA)的危险因素和自然病史,AKOA 定义为从无影像学膝关节骨关节炎转变为晚期疾病<4 年,并将这些发现与典型骨关节炎(缓慢进展性疾病)、衰老、既往病例报告/系列以及相关动物模型进行了对比。在 AKOA 出现(发病)前的 2 到 4 年内,其危险因素包括年龄较大、体重指数较高、关节对线改变、对侧骨关节炎、更严重的影像学前疾病负担(结构、症状和功能)或空腹血糖较低。在 AKOA 发病前 1 到 2 年内,患者常出现关节软骨快速丢失、更大的骨髓病变和滑液-滑膜炎、更多的半月板病变、更慢的椅子站立或行走速度以及更大的关节炎对全球的影响,与典型膝关节骨关节炎患者相比。关节症状增加使患者易发生新的关节创伤,对于发生 AKOA 的患者,这种创伤通常表现为不稳定的半月板撕裂(如放射状或根部撕裂)。在 9 年期间,有 1/7 的 AKOA 发病患者随后接受了膝关节置换。从任何影像学严重程度增加到膝关节置换的中位时间仅为 2.3 年。尽管存在一些相似之处,但 AKOA 与其他快速进展性关节病不同,在进行进一步的比较研究之前,不应将这些现象混为一谈或从一种类型的骨关节炎中提取结果应用于另一种类型的骨关节炎。在存在其他危险因素或关节负荷分布不均匀的情况下,诱导半月板损伤或创建关节的动物模型与其他模型相比会产生加速形式的骨关节炎,并且可能为 AKOA 提供深入的见解。
结论:加速性膝关节骨关节炎与典型膝关节骨关节炎不同。在 Osteoarthritis Initiative 和 Chingford 研究中,AKOA 的发病率相当高。在流行病学研究和临床试验中需要考虑并研究 AKOA。
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