Department of Rheumatology, The Rheumatology Research Unit, Odense University Hospital and University of Southern Denmark, Odense, Denmark.
Department of Rheumatology, Silkeborg Hospital, Silkeborg, Denmark.
Clin Exp Rheumatol. 2020 Jan-Feb;38(1):122-128. Epub 2019 Aug 27.
To study circulating MFAP4 in rheumatoid arthritis (RA) and its associations with clinical phenotype.
Early RA (ERA): 47 patients with newly diagnosed, treatment naïve RA were included. Serum MFAP4, clinical and laboratory disease variables were recorded serially during 12 months of intensive synovitis suppressive treatment. Long-standing RA (LRA): 317 patients participated, all receiving DMARD treatment. Disease activity, autoantibody status, extra-articular manifestations and cardiovascular morbidity were recorded. Paired serum and synovial fluid samples were obtained from 13 untreated ERA patients. Healthy blood donors served as reference points. MFAP4 was quantified by AlphaLISA immunoassay. Univariate, multivariate and mixed effects regression models were applied in the statistical analysis.
ERA: MFAP4 increased from baseline and was significantly elevated at the 12-month follow-up, 17.8 U/l [12.6;24.1] vs. healthy controls, 12.7 U/l [9.5;15.6], p<0.001. MFAP4 did not correlate with joint counts or C-reactive protein. LRA: MFAP4 was increased, 25.9 U/l [20.4;33.7] vs. healthy controls, 17.6 U/l [13.7;21.2], p<0.0001, but did not correlate with disease activity measures or presence of extra-articular manifestations. Notably, MFAP4 correlated inversely with smoking (p<0.0001) and presence of antibodies against cyclic citrullinated peptides (anti-CCP), p=0.005. There was a positive association with systolic blood pressure, p=0.001 and co-occurrence of three cardiovascular events and/or risk factors, p<0.0001. The serum:synovial fluid MFAP4 ratio was 2:1.
MFAP4 increases from diagnostic baseline despite intensive treatment but does not associate with synovitis at early or late stages of RA. Correlation patterns indicate that increased MFAP4 may reflect enhanced RA-related vascular remodelling.
研究类风湿关节炎(RA)患者循环 MFAP4 及其与临床表型的相关性。
早期 RA(ERA):纳入 47 例新诊断、未接受治疗的 RA 患者。在 12 个月的强化滑膜抑制治疗期间,连续记录血清 MFAP4、临床和实验室疾病变量。长期 RA(LRA):共 317 例患者参与,均接受 DMARD 治疗。记录疾病活动度、自身抗体状态、关节外表现和心血管发病率。从 13 例未经治疗的 ERA 患者中获得配对的血清和滑膜液样本。健康献血者作为参考点。采用 AlphaLISA 免疫分析法测定 MFAP4。在统计分析中应用了单变量、多变量和混合效应回归模型。
ERA:MFAP4 从基线开始升高,在 12 个月的随访时显著升高,17.8 U/l [12.6;24.1] vs. 健康对照组 12.7 U/l [9.5;15.6],p<0.001。MFAP4 与关节计数或 C 反应蛋白无相关性。LRA:MFAP4 升高,25.9 U/l [20.4;33.7] vs. 健康对照组 17.6 U/l [13.7;21.2],p<0.0001,但与疾病活动度测量或关节外表现无关。值得注意的是,MFAP4 与吸烟呈负相关(p<0.0001)和抗环瓜氨酸肽抗体(抗-CCP)的存在呈正相关,p=0.005。MFAP4 与收缩压呈正相关,p=0.001,与三种心血管事件和/或危险因素同时发生呈正相关,p<0.0001。血清:滑膜液 MFAP4 比值为 2:1。
尽管进行了强化治疗,但 MFAP4 从诊断时开始升高,但与 RA 的早期或晚期滑膜炎无关。相关模式表明,MFAP4 的增加可能反映了增强的 RA 相关血管重塑。