The association between systemic inflammation as measured by calprotectin and autoantibody load in rheumatoid arthritis

IF 9.9 1区 医学 Q1 RHEUMATOLOGY
Caroline Grönwall,Linda Mathsson Alm,Helga Westerlind,Isabel Gehring,Nasim Ghasemzadeh,Niels Steen Krogh,Siri Lillegraven,Espen Haavardsholm,Martina Johannesson,Tore K. Kvien,Johan Rönnelid,Tue Wenzel Kragstrup,Bente Glintborg,Merete Lund Hetland,Hilde Berner Hammer,The Danish Rheumatologic Biobank Study Group, Swedish Rheumatology Quality Register Biobank Study Group(SRQb),Johan Askling,Oliver Hendricks,Estrid Høgdall,Dorte Vendelbo Jensen,Heidi Lausten Munk,Jens Kristian Pedersen,Torkell Ellingsen,Anne Gitte Loft,Ellen‐Margrethe Hauge,Salome Kristensen,Lene Dreyer,Asta Linauskas,Søren Jacobsen,Carl Turesson,Solbritt Rantapää Dahlqvist,Lena Björkman,Alf Kastbom,Eva Baecklund
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引用次数: 0

Abstract

Background Plasma calprotectin is a marker of neutrophil activity. Its relation to the clinical phenotype and autoantibodies in rheumatoid arthritis (RA) is only partly understood. We therefore aimed to investigate the association between calprotectin and clinical parameters, CRP, ESR, anti‐CCP2 and other anti‐modified protein autoantibodies (AMPAs) in patients with RA. Methods Rheumatoid factor (RF), anti‐cyclic citrullinated peptide 2 (CCP2) isotypes and plasma calprotectin were centrally measured in a cross‐sectional cohort of 4521 Scandinavian RA patients using fluoroenzyme immunoassays. IgG to 15 citrullinated (Cit) and four carbamylated or acetylated (Carb/Acet) peptides were measured by multiplex solid‐phase array. CRP and ESR values were obtained from clinical measurements at the time of blood sampling. Results Calprotectin levels correlated with ESR (ρ=0.53), CRP (ρ=0.47), VAS pain (ρ=0.24), SJC28 (ρ=0.39), and TJC28 (ρ=0.26; p<0.0001 for all). Patients with both elevated CRP (>10mg/L) and calprotectin (>15 AU/ml) (14%, N=613) had significantly higher VAS pain, SJC28, and TJC28 than patients with only elevated CRP (p<0.0001), in early and established disease. Patients with elevated calprotectin, independent of CRP levels, had significantly higher proportions of AMPA positivity including anti‐CCP2. When patients were divided into six groups based on increasing number of Cit/Carb/Acet‐reactivities and anti‐CCP2 IgG levels, elevated calprotectin was associated with increasing AMPA load, particularly in the presence of RF IgM. The differences between AMPA load groups remained after adjusting for sex, age, RF IgM, and disease duration. Conclusions Plasma calprotectin is positively associated with seropositivity and AMPA load by autoantibody levels and the breadth of the autoantibody response.
类风湿关节炎中钙保护蛋白测量的全身炎症与自身抗体负荷之间的关系
血浆钙保护蛋白是中性粒细胞活性的标志。它与类风湿关节炎(RA)的临床表型和自身抗体的关系仅部分了解。因此,我们旨在研究钙保护蛋白与RA患者临床参数、CRP、ESR、抗CCP2和其他抗修饰蛋白自身抗体(AMPAs)之间的关系。方法采用氟酶免疫分析法对4521例斯堪的纳维亚类风湿性关节炎患者的横断面队列进行类风湿因子(RF)、抗环瓜氨酸肽2 (CCP2)同型和血浆钙保护蛋白的检测。IgG对15个瓜氨酸化(Cit)和4个氨基甲酰化或乙酰化(Carb/Acet)肽进行测定。CRP和ESR值在采血时通过临床测量获得。结果钙保护蛋白水平与ESR (ρ=0.53)、CRP (ρ=0.47)、VAS疼痛(ρ=0.24)、SJC28 (ρ=0.39)、TJC28 (ρ=0.26; p<;均为0.0001)相关。在早期和确诊疾病中,CRP (10mg/L)和钙保护素(15au /ml)升高的患者(14%,N=613)的VAS疼痛、SJC28和TJC28明显高于仅CRP升高的患者(0.0001)。钙保护蛋白升高的患者,与CRP水平无关,AMPA阳性的比例明显更高,包括抗CCP2。当根据Cit/Carb/Acet反应性和抗CCP2 IgG水平的增加将患者分为六组时,钙保护蛋白升高与AMPA负荷增加有关,特别是在RF IgM存在的情况下。在调整性别、年龄、RF IgM和疾病持续时间后,AMPA负荷组之间的差异仍然存在。结论血浆钙保护蛋白与血清阳性和AMPA负荷与自身抗体水平和自身抗体反应广度呈正相关。
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来源期刊
Arthritis & Rheumatology
Arthritis & Rheumatology RHEUMATOLOGY-
CiteScore
20.90
自引率
3.00%
发文量
371
期刊介绍: Arthritis & Rheumatology is the official journal of the American College of Rheumatology and focuses on the natural history, pathophysiology, treatment, and outcome of rheumatic diseases. It is a peer-reviewed publication that aims to provide the highest quality basic and clinical research in this field. The journal covers a wide range of investigative areas and also includes review articles, editorials, and educational material for researchers and clinicians. Being recognized as a leading research journal in rheumatology, Arthritis & Rheumatology serves the global community of rheumatology investigators and clinicians.
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