George Navya, Liew Jean W, Wang Na, Tilley Sarah, Guermazi Ali, Lynch John, Lewis Cora, Torner James, Neogi Tuhina
Department of Internal Medicine, Boston University Chobanian & Avedisian School of Medicine, Boston, MA, United States.
Section of Rheumatology, Boston University Chobanian & Avedisian School of Medicine, Boston, MA, United States.
Osteoarthritis Cartilage. 2025 Sep 5. doi: 10.1016/j.joca.2025.08.019.
Posthoc analysis of a canakinumab trial showed a risk reduction of joint replacement in participants with cardiac disease and elevated hsCRP (≥2mg/dL). We determined if hsCRP could serve as a marker to identify an inflammatory OA phenotype characterized by intra-articular synovitis.
We used data from the NIH-funded MOST Study, where participants had baseline knee MRIs and hsCRP assays. Inflammation was scored using the Whole Organ MRI Score (WORMS), with presence defined as Hoffa's synovitis or effusion-synovitis score ≥2 in ≥1 of 3 locations. We examined the relationship between hsCRP and inflammation presence using logistic regression, and the average inflammation score with linear regression. Analyses were repeated with hsCRP categorized as ≥2mg/dL vs. <2mg/dL. Cubic spline regression and ROC curve were completed. Analyses were adjusted for age, sex, and body mass index.
Out of 792 participants (mean age 62, 52% female), mean hsCRP was 2.98 mg/dL, with 41% having hsCRP ≥2mg/dL. Inflammation was present in 28% of knees. No association was found between hsCRP levels and inflammation presence (odds ratio 0.99, 95% confidence interval 0.96-1.01) or average score, including with dichotomized hsCRP. Cubic spline regression did not reveal non-linear associations. The ROC curve suggested poor predictive ability of hsCRP to identify knees with inflammation on MRI.
Despite interest in identifying an inflammatory phenotype in OA, hsCRP levels do not reliably identify knees with inflammation. Further investigation is needed to determine if hsCRP can predict knee response to therapies targeting inflammation not directly related to synovitis.
一项关于卡那单抗的试验的事后分析显示,患有心脏病且高敏C反应蛋白(hsCRP)升高(≥2mg/dL)的参与者进行关节置换的风险降低。我们确定hsCRP是否可作为一种标志物,用于识别以关节内滑膜炎为特征的炎症性骨关节炎表型。
我们使用了美国国立卫生研究院资助的MOST研究中的数据,该研究中的参与者进行了基线膝关节磁共振成像(MRI)和hsCRP检测。使用全器官MRI评分(WORMS)对炎症进行评分,存在炎症定义为在三个部位中的至少一个部位出现 Hoffa 滑膜炎或积液 - 滑膜炎评分≥2。我们使用逻辑回归分析hsCRP与炎症存在之间的关系,并使用线性回归分析平均炎症评分。将hsCRP分为≥2mg/dL与<2mg/dL进行重复分析。完成三次样条回归和ROC曲线分析。分析对年龄、性别和体重指数进行了校正。
在792名参与者(平均年龄62岁,52%为女性)中,平均hsCRP为2.98mg/dL,41%的参与者hsCRP≥2mg/dL。28%的膝关节存在炎症。未发现hsCRP水平与炎症存在(优势比0.99,95%置信区间0.96 - 1.01)或平均评分之间存在关联,包括二分法hsCRP分析。三次样条回归未显示非线性关联。ROC曲线表明hsCRP识别MRI上有炎症的膝关节的预测能力较差。
尽管人们对识别骨关节炎中的炎症表型感兴趣,但hsCRP水平不能可靠地识别有炎症的膝关节。需要进一步研究以确定hsCRP是否能够预测膝关节对针对与滑膜炎无直接关系的炎症的治疗的反应。