Association between anti-collagen type II autoantibodies and the acute rheumatoid arthritis phenotype in a cohort of rheumatoid arthritis patients
DOI:
https://doi.org/10.15419/bmrat.v9i4.736Keywords:
Rheumatoid Arthritis, Anticollagen type II antibodies, Disease Activity Score, Acute rheumatoid arthritis phenotypeAbstract
Background: This study aims to evaluate serum concentrations of anti-collagen type II (anti-CII) antibodies in Iraqi patients with a severe rheumatoid arthritis (RA) phenotype and investigate the relationship between higher concentrations of anti-CII antibodies and higher levels of inflammation.
Methods: This study was conducted with 100 patients with RA who were admitted to the Arthritis Consulting Clinic, Baghdad Teaching Hospital, Iraq. The patients selected were patients diagnosed with RA about 2 to 3 years ago. Data on the patients were collected, including the results of tests for anti-CII concentrations, and were compared with data from 30 healthy subjects. Healthcare workers aspirated 5 ml of blood from each control and patient subject, divided into two parts. The workers transferred the first one (3 ml) into a plain tube, allowed 30 minutes for it to clot, and then isolated the serum by centrifugation at 2500 rpm for 10 minutes for measurement of the anti-collagen type II antibodies by enzyme-linked immunosorbent assay (ELISA). The workers transferred the second part (2 ml) to the tube containing EDTA for hematological measurement of the erythrocyte sedimentation rate (ESR).
Results: This study found that the levels of anti-collagen type II antibodies were significantly higher in patients with RA than in healthy controls (p-value > 0.05). The study found a statistically significant positive moderate correlation with ESR (r = 0.56, p-value = 0.000) and a statistically significant positive strong correlation between disease activity score-28 (DAS28) and anti-collagen type II antibodies (r = 0.65, p-value = 0.000) in RA patients.
Conclusions: Anti-CII antibodies can be considered an important parameter for the early detection of RA and can be used to determine the activity of RA.
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Copyright The Author(s) 2017. This article is published with open access by BioMedPress. This article is distributed under the terms of the Creative Commons Attribution License (CC-BY 4.0) which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.