Boeters Debbie M, Mangnus Lukas, Ajeganova Sofia, Lindqvist Elisabet, Svensson Björn, Toes René E M, Trouw Leendert A, Huizinga Tom W J, Berenbaum Francis, Morel Jacques, Rantapää-Dahlqvist Solbritt, van der Helm-van Mil Annette H M
Department of Rheumatology C1-R, Leiden University Medical Center, PO Box 9600, Leiden, 2300RC, The Netherlands.
Department of Medicine Huddinge, Karolinska Institutet, Stockholm, Sweden.
Arthritis Res Ther. 2017 May 31;19(1):115. doi: 10.1186/s13075-017-1324-y.
Rheumatoid arthritis (RA) consists of two syndromes, one autoantibody-positive and one autoantibody-negative. Existing data on the relation between age of onset and prevalence of autoantibodies were conflicting. Therefore this multicohort study assessed the age of onset in relation to the presence of autoantibodies. The association with characteristics of the anti-citrullinated protein antibodies (ACPA) response was also explored.
The 1987 criteria-positive RA patients included in the Leiden EAC, BARFOT, ESPOIR, Umeå and Lund cohorts (n = 3321) were studied at presentation for age of onset and the presence of ACPA, rheumatoid factor (RF) and anti-carbamylated protein (anti-CarP) antibodies. Logistic regression analyses were performed; effect sizes were summarized in inverse-weighted meta-analyses. Within ACPA-positive RA, ACPA level was studied in all cohorts; ACPA isotypes, ACPA fine specificity and ACPA avidity index and clinical characteristics were studied in the Leiden EAC.
From the age of 50 onward, the proportion of ACPA-negative RA patients increased with age in the five cohorts. Similar observations were made for RF and anti-CarP. The composition of the ACPA response did not change with increasing age of onset with respect to titer, isotype distribution, fine specificity and avidity index. With increasing age of onset, RA patients smoked less often, had higher acute phase reactants and more often had a sub(acute) symptom onset.
Data of five cohorts revealed that with older age of onset ACPA-negative RA is more frequent than ACPA-positive RA, while characteristics of ACPA-positive RA as judged by the composition of the ACPA response appeared not age dependent. Further biologic studies are needed to characterize the pathogenesis of ACPA-negative polyarthritis at older age and to promote personalized treatment decisions in ACPA-negative patients in daily practice.
类风湿关节炎(RA)由两种综合征组成,一种为自身抗体阳性,另一种为自身抗体阴性。关于发病年龄与自身抗体患病率之间关系的现有数据相互矛盾。因此,这项多队列研究评估了发病年龄与自身抗体存在情况的关系。还探讨了与抗瓜氨酸化蛋白抗体(ACPA)反应特征的关联。
对纳入莱顿EAC、BARFOT、ESPOIR、于默奥和隆德队列的1987年标准阳性RA患者(n = 3321)进行研究,记录其发病年龄以及ACPA、类风湿因子(RF)和抗氨甲酰化蛋白(抗CarP)抗体的存在情况。进行了逻辑回归分析;效应量在逆加权荟萃分析中进行总结。在ACPA阳性的RA患者中,对所有队列研究了ACPA水平;在莱顿EAC中研究了ACPA亚型、ACPA精细特异性、ACPA亲和力指数和临床特征。
在这五个队列中,从50岁起,ACPA阴性RA患者的比例随年龄增加而上升。RF和抗CarP也有类似观察结果。就滴度、亚型分布、精细特异性和亲和力指数而言,ACPA反应的组成并未随发病年龄的增加而改变。随着发病年龄的增加,RA患者吸烟频率降低,急性期反应物水平升高,且更常出现亚(急)性症状发作。
五个队列的数据显示,随着发病年龄的增加,ACPA阴性RA比ACPA阳性RA更常见,而根据ACPA反应组成判断的ACPA阳性RA特征似乎与年龄无关。需要进一步的生物学研究来阐明老年ACPA阴性多关节炎的发病机制,并在日常实践中促进ACPA阴性患者的个性化治疗决策。