The prevalence of ACPA is lower in rheumatoid arthritis patients with an older age of onset but the composition of the ACPA response appears identical

被引:23
作者
Boeters, Debbie M. [1 ]
Mangnus, Lukas [1 ]
Ajeganova, Sofia [1 ,2 ]
Lindqvist, Elisabet [3 ,4 ]
Svensson, Bjorn [3 ]
Toes, Rene E. M. [1 ]
Trouw, Leendert A. [1 ]
Huizinga, Tom W. J. [1 ]
Berenbaum, Francis [5 ]
Morel, Jacques [6 ,7 ]
Rantapaa-Dahlqvist, Solbritt [8 ]
van der Helm-van Mil, Annette H. M. [1 ]
机构
[1] Leiden Univ, Med Ctr, Dept Rheumatol R C1, POB 9600, NL-2300 RC Leiden, Netherlands
[2] Karolinska Inst, Dept Med Huddinge, Stockholm, Sweden
[3] Lund Univ, Sect Rheumatol, Dept Clin Sci, Lund, Sweden
[4] Skane Univ Hosp, Lund, Sweden
[5] Sorbonne Univ, INSERM, St Antoine Hosp, AP HP,Dept Rheumatol,UMR S938,DHU i2B, Paris, France
[6] Teaching Hosp Lapeyronie, Dept Rheumatol, Montpellier, France
[7] Montpellier Univ, Montpellier, France
[8] Univ Hosp, Dept Publ Hlth & Clin Med Rheumatol, Umea, Sweden
关键词
Rheumatoid arthritis; Age; Autoantibodies; ACPA characteristics; RADIOGRAPHIC JOINT DAMAGE; SHARED EPITOPE ALLELES; ANTI-CCP ANTIBODIES; PROGRESSION; DISEASE; ASSOCIATION; COHORT; AUTOANTIBODIES; DESTRUCTION; VARIANTS;
D O I
10.1186/s13075-017-1324-y
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: 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. Methods: The 1987 criteria-positive RA patients included in the Leiden EAC, BARFOT, ESPOIR, Ume (a) over circle 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. Results: 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. Conclusions: 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.
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页数:10
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