Clinic of Internal Medicine, University of Tartu, L.Puusepa 6-222, Tartu 51014, Estonia.
Rheumatol Int. 2013 Apr;33(4):903-11. doi: 10.1007/s00296-012-2463-8. Epub 2012 Jul 21.
To determine the possible diagnostic and prognostic value of cartilage biomarkers in early-stage progressive and nonprogressive knee osteoarthritis (OA) in a population-based cohort of middle-aged subjects with chronic knee pain. Design tibiofemoral (TF) and patellofemoral (PF) radiographs were graded in 128 subjects (mean age at baseline, 45 ± 6.2 years) in 2002, 2005, and 2008. Cartilage degradation was assessed by urinary C-telopeptide fragments of type II collagen (uCTx-II), synthesis by serum type II A procollagen N-terminal propeptide (sPIIANP), and articular tissue turnover in general by cartilage oligomeric matrix protein (sCOMP). Several diagnostic associations were found between all studied biomarkers and progressive osteophytosis. COMP and CTx-II had a predictive value for subsequent progressive osteophytosis in multiple knee compartments and in case of CTx-II-also for progressive JSN. Over the first 3 years (2002-2005), significant associations were observed between COMP and progressive osteophytosis, whereas 3 years later (2005-2008) between CTx-II and progressive JSN. Thus, the associations between cartilage markers (COMP, CTx-II) and progression of radiographic OA features--osteophytes and JSN--were different between 2002-2005 and 2005-2008. Logistic regression revealed that for every unit increase in COMP level, there was 33 % higher risk for TF osteophyte progression. During early-stage OA, the presence and progression of osteophytosis is accompanied by increased level of cartilage biomarkers. This is the first study to demonstrate biochemical differences over the course of knee OA, illustrating a phasic nonpersistent character of OA with periods of progression and stabilization.
为了确定在患有慢性膝关节疼痛的中年人群中,基于人群的队列中,早期进展性和非进展性膝关节骨关节炎(OA)中软骨生物标志物的可能诊断和预后价值。 在 2002 年、2005 年和 2008 年对 128 名受试者(基线时平均年龄为 45±6.2 岁)的胫股(TF)和髌股(PF)进行放射照相分级。 通过尿型 II 胶原 C 端肽(uCTX-II)评估软骨降解,通过血清 II 型 A 前胶原 N 端前肽(sPIIANP)评估合成,通过软骨寡聚基质蛋白(sCOMP)评估一般关节组织转化。 在所有研究的生物标志物中,都发现了几种与进展性骨赘形成有关的诊断关联。 COMP 和 CTx-II 对多个膝关节腔的随后进展性骨赘形成以及 CTx-II 的情况下的进行性 JSN 具有预测价值。 在最初的 3 年(2002-2005 年)中,COMP 与进展性骨赘形成之间存在显着关联,而 3 年后(2005-2008 年)CTx-II 与进行性 JSN 之间存在关联。 因此,在 2002-2005 年和 2005-2008 年之间,软骨标志物(COMP,CTX-II)与放射学 OA 特征(骨赘和 JSN)进展之间的关联有所不同。 逻辑回归显示,COMP 水平每增加一个单位,TF 骨赘进展的风险就增加 33%。 在早期 OA 中,骨赘的存在和进展伴随着软骨生物标志物水平的升高。 这是第一项证明膝关节 OA 过程中存在生化差异的研究,表明 OA 具有阶段性的非持续性特征,具有进展和稳定期。