Abstract

Determination of anti-citrullinated peptide antibodies (ACPA) plays a relevant role in the diagnosis of rheumatoid arthritis (RA). To date, it is still unclear if the use of several tests for these autoantibodies in the same patient offers additional value as compared to performing only one test. Therefore, we evaluated the performance of using two assays for ACPA: second-generation anti-citrullinated cyclic peptides antibodies (anti-CCP2) and anti-mutated citrullinated vimentin (anti-MCV) antibodies for the diagnosis of RA. We compared three groups: RA (n = 142), chronic inflammatory disease (CIRD, n = 86), and clinically healthy subjects (CHS, n = 56) to evaluate sensitivity, specificity, predictive values, and likelihood ratios (LR) of these two assays for the presence of RA. A lower frequency of positivity for anti-CCP2 was found in RA (66.2%) as compared with anti-MCV (81.0%). When comparing RA versus other CIRD, sensitivity increased when both assays were performed. This strategy of testing both assays had high specificity and LR+. We conclude that adding the assay of anti-MCV antibodies to the determination of anti-CCP2 increases the sensitivity for detecting seropositive RA. Therefore, we propose the use of both assays in the initial screening of RA in longitudinal studies, including early onset of undifferentiated arthritis.

Highlights

  • Rheumatoid arthritis (RA) is a chronic inflammatory disorder that involves synovial joints and may develop extraarticular manifestations [1]

  • Assays to identify antibodies against citrullinated cyclic peptides are commonly used as a tool to support the diagnosis of RA, because it has been widely demonstrated that these autoantibodies have higher specificity as compared with the rheumatoid factor (RF)

  • Additional data, not shown in this table, include that 83% of patients with RA had an active disease (DAS-28 index >3.2) and 26.6% had a significant degree of disability (HAQDI > 1.25)

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Summary

Introduction

Rheumatoid arthritis (RA) is a chronic inflammatory disorder that involves synovial joints and may develop extraarticular manifestations [1]. The diagnosis of RA may pose some difficulties in primary care, during early disease, and this disease may inappropriately be confused with other rheumatic diseases [2] In this context, a relevant tool to support the diagnosis is the presence of autoantibodies associated with the disease. The detection of rheumatoid factor [3] is useful to support the diagnosis and it is detected in 75% of patients with RA, a limitation of this autoantibody is its low specificity, being frequently observed in other rheumatic disorders, chronic infections, and even in healthy elderly people [3]. Assays to identify antibodies against citrullinated cyclic peptides are commonly used as a tool to support the diagnosis of RA, because it has been widely demonstrated that these autoantibodies have higher specificity as compared with the rheumatoid factor (RF). Around 38% of patients with RA may have negative results for anti-CCP2 [5, 6]

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