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在根据 2010 年 ACR/EULAR 标准分类的初治 DMARD 患者队列中,与血清阳性 RA 患者相比,血清阴性 RA 患者的炎症活动度更高。

Patients with seronegative RA have more inflammatory activity compared with patients with seropositive RA in an inception cohort of DMARD-naïve patients classified according to the 2010 ACR/EULAR criteria.

机构信息

Department of Rheumatology, Diakonhjemmet Hospital, Oslo, Norway.

Department of Rheumatology, Haukeland University Hospital, Bergen, Norway.

出版信息

Ann Rheum Dis. 2017 Feb;76(2):341-345. doi: 10.1136/annrheumdis-2015-208873. Epub 2016 Apr 19.

Abstract

OBJECTIVES

To compare the presentation of seropositive and seronegative early rheumatoid arthritis (RA) in disease-modifying antirheumatic drug (DMARD)-naïve patients classified according to the 2010 American College of Rheumatology (ACR)/European League Against Rheumatism (EULAR) criteria.

METHODS

All patients had symptom duration from first swollen joint <2 years and were DMARD naïve with an indication for DMARD treatment. Patients were stratified as seropositive (positive rheumatoid factor (RF)+ and/or anticitrullinated peptide antibody (ACPA)+) or seronegative (RF- and ACPA-), and disease characteristics were compared between groups.

RESULTS

A total of 234 patients were included, and 36 (15.4%) were seronegative. Ultrasonography (US) scores for joints (median 55 vs 25, p<0.001) and tendons (median 3 vs 0, p<0.001), number of swollen joints (median 17 vs 8, p<0.001), disease activity score (DAS; mean 3.9 vs 3.4, p=0.03) and physician global assessment (mean 49.1 vs 38.9, p=0.006) were significantly higher in seronegative patients compared with seropositive. Total van der Heijde-modified Sharp score, Richie Articular Index and patient-reported outcome measures were similar between groups.

CONCLUSIONS

Seronegative patients had higher levels of inflammation, assessed both clinically and by US, than seropositive patients. These differences may reflect the high number of involved joints required for seronegative patients to fulfil the 2010 ACR/EULAR classification criteria for RA.

TRIAL REGISTRATION NUMBER

NCT01205854; Pre-results.

摘要

目的

比较根据 2010 年美国风湿病学会(ACR)/欧洲抗风湿病联盟(EULAR)标准分类的初诊、未使用疾病修饰抗风湿药物(DMARD)的血清阳性和血清阴性早期类风湿关节炎(RA)患者的表现。

方法

所有患者的首关节肿胀时间<2 年,且均为初诊、未使用 DMARD,有使用 DMARD 的指征。患者分为血清阳性(RF 阳性和/或 ACPA 阳性)或血清阴性(RF 阴性和 ACPA 阴性),比较两组间的疾病特征。

结果

共纳入 234 例患者,其中 36 例(15.4%)为血清阴性。血清阴性患者的关节(中位数 55 分比 25 分,p<0.001)和肌腱(中位数 3 分比 0 分,p<0.001)的超声评分、肿胀关节数(中位数 17 比 8,p<0.001)、疾病活动评分(DAS;均值 3.9 比 3.4,p=0.03)和医生总体评估(均值 49.1 比 38.9,p=0.006)均显著高于血清阳性患者。总的 van der Heijde 改良 Sharp 评分、Richie 关节指数和患者报告的结局测量值在两组间相似。

结论

与血清阳性患者相比,血清阴性患者的炎症水平更高,无论是临床评估还是超声评估。这些差异可能反映了血清阴性患者需要更多的受累关节才能符合 2010 年 ACR/EULAR 的 RA 分类标准。

试验注册编号

NCT01205854;预注册结果。

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