Gavrilă B I, Ciofu C, Stoica V
Department of Internal Medicine and Rheumatology, "Dr. I. Cantacuzino" Clinical Hospital, Bucharest, Romania; "Carol Davila" University of Medicine and Pharmacy, Bucharest, Romania.
J Med Life. 2016 Apr-Jun;9(2):144-8.
Rheumatoid arthritis (RA) is a chronic inflammatory disease with autoimmune pathogenesis. It affects mainly small joints (of the hands and feet) and has many systemic manifestations. Studying biomarkers in rheumatology intensely appeared from the need to understand the mechanisms underlying some rheumatic diseases. Discovering new biomarkers with key roles in various stages of evolution, remains a subject of interest for RA. Currently, according to the EULAR 2010 criteria, the rheumatoid factor (RF) and the anti-cyclic citrullinated peptide (anti-CCP) are used for RA diagnosis. Since 2010, new biomarkers were discovered and proved useful in identifying RA in early stages. For a more rigorous management of these cases, one of the key steps in the evolution of patients with RA is to recognize and distinguish the more aggressive forms of the disease through prognostic biomarkers. "Treat to target" recommends the use of 3 composite scores to monitor the evolution of the disease: disease activity score (DAS 28), simple disease activity index (SDAI) and clinical disease activity index (CDAI), but, a new test was developed which better monitors the disease activity. The introduction of biological therapies has revolutionized the treatment of RA. Despite these advances, 20-40% of the patients are declared nonresponders to at least one of the therapies. The patient exposure to the potential side effects and high costs requires the discovery of a biomarker that could identify those who can benefit from the pretreatment of a certain therapy.
RA = rheumatoid arthritis, RF = rheumatoid factor, DAS 28 = disease activity score, SDAI = simple disease activity index, CDAI = clinical disease activity index, ACR = American College of Rheumatology, EULAR = European League against Rheumatism, anti-CCP = antibodies against cyclic citrullinated proteins, anti-MCV = mutated citrullinated vimentin antibodies, anti-CarP = antibodies against carbamylated proteins, MBDA = multi biomarker disease activity test, COMP = cartilage oligomeric matrix protein, ADAs = antidrug antibodies, CDA = clinical disease activity index, SDAI = simplified disease activity index, ESR = erythrocyte sedimentation rate, CRP = C reactive protein, SAA = serum amyloid A, VCAM-1 = vascular cell adhesion molecule-1, IL-6 = interleukin-6, TNF-R1 = tumor necrosis factor receptor 1, EGF = epidermal growth factor, VEGF-A = vascular endothelial growth factor A.
类风湿关节炎(RA)是一种具有自身免疫发病机制的慢性炎症性疾病。它主要影响(手和脚的)小关节,并具有多种全身表现。出于理解某些风湿性疾病潜在机制的需要,在风湿病学领域对生物标志物进行了深入研究。发现能在疾病演变的各个阶段发挥关键作用的新生物标志物,仍是类风湿关节炎研究的一个热点。目前,根据2010年欧洲抗风湿病联盟(EULAR)标准,类风湿因子(RF)和抗环瓜氨酸肽(抗CCP)用于类风湿关节炎的诊断。自2010年以来,已发现一些新的生物标志物,并证明它们在早期类风湿关节炎的识别中很有用。为了更严格地管理这些病例,类风湿关节炎患者病情演变的关键步骤之一是通过预后生物标志物识别和区分疾病更具侵袭性的形式。“达标治疗”推荐使用3种综合评分来监测疾病进展:疾病活动评分(DAS28)、简化疾病活动指数(SDAI)和临床疾病活动指数(CDAI),但已经开发出一种能更好地监测疾病活动的新检测方法。生物疗法的引入彻底改变了类风湿关节炎的治疗方式。尽管有这些进展,但仍有20% - 40%的患者被宣布对至少一种治疗无反应。患者面临潜在的副作用和高昂的费用,这就需要发现一种生物标志物,能够识别那些可以从某种治疗的预处理中获益的患者。
RA = 类风湿关节炎,RF = 类风湿因子,DAS28 = 疾病活动评分,SDAI = 简化疾病活动指数,CDAI = 临床疾病活动指数,ACR = 美国风湿病学会,EULAR = 欧洲抗风湿病联盟,抗CCP = 抗环瓜氨酸化蛋白抗体,抗MCV = 抗突变瓜氨酸波形蛋白抗体,抗CarP = 抗氨甲酰化蛋白抗体,MBDA = 多生物标志物疾病活动检测,COMP = 软骨寡聚基质蛋白,ADAs = 抗药物抗体,CDA = 临床疾病活动指数,SDAI = 简化疾病活动指数,ESR = 红细胞沉降率,CRP = C反应蛋白,SAA = 血清淀粉样蛋白A,VCAM - 1 = 血管细胞黏附分子 - 1,IL - 6 = 白细胞介素 - 6,TNF - R1 = 肿瘤坏死因子受体1,EGF = 表皮生长因子,VEGF - A = 血管内皮生长因子A