FRI0075 Effects of Dmards on Citrullinated Peptide Autoantibody Levels in RA Patients- A Longitudinal Analysis. (15th July 2016)
- Record Type:
- Journal Article
- Title:
- FRI0075 Effects of Dmards on Citrullinated Peptide Autoantibody Levels in RA Patients- A Longitudinal Analysis. (15th July 2016)
- Main Title:
- FRI0075 Effects of Dmards on Citrullinated Peptide Autoantibody Levels in RA Patients- A Longitudinal Analysis
- Authors:
- Schett, G.
Wunderlich, C.
Figueiredo, C.
Cobra, J.F.
Hueber, A.J.
Kleyer, A.
Rech, J. - Abstract:
- Abstract : Background: Anti-citrullinated cyclic peptide 2 (CCP2) antibodiy levels are considered to be highly stable during disease-modifying anti-rheumatic drug (DMARD) therapy of rheumatoid arthritis (RA). However, no studies have actually analyzed sequential anti-CCP2 antibody levels during various DMARD therapies in a controll manner Objectives: To study whether stable treatment with DMARDs affects anti-CCP2 antibody levels in patients with rheumatoid arthritis. Methods: In this longitudinal observational study 100 RA patients were followed for anti-CCP2 IgG antibody (U/L) and total IgG level (mg/dL) every 6 months for a total period of 2.5 years. All patients received stable DMARD treatment during this period. Five groups comprising each 20 patients were analysed: (1) methotrexate (MTX) alone, (2) tumor necrosis factor inhibitors (TNFi), (3) tocilizumab (TCZ), (4) rituximab (RTX) and (5) abatacept (ABA). Results: Baseline demographic and disease-specific characteristics were comparable between the 5 groups. Anti-CCP2 antibody levels did not show significant changes in patients treated with MTX (mean±SEM: -24.1±8.1%), TNFi (-14.0±11.1%) or TCZ (-24.3±11.3%) between baseline and the 2, 5 years follow up. In contrast, anti-CCP2 antibody levels significantly decreased during treatment with RTX (-75.6±4.4%) and ABA (-82.5±3.7%). With respect to total IgG levels, no significant changes were observed with MTX (-24.1±8.1%), TNFi (-14.0±11.1%) or TCZ (-24.3±11.3%) over 2, 5Abstract : Background: Anti-citrullinated cyclic peptide 2 (CCP2) antibodiy levels are considered to be highly stable during disease-modifying anti-rheumatic drug (DMARD) therapy of rheumatoid arthritis (RA). However, no studies have actually analyzed sequential anti-CCP2 antibody levels during various DMARD therapies in a controll manner Objectives: To study whether stable treatment with DMARDs affects anti-CCP2 antibody levels in patients with rheumatoid arthritis. Methods: In this longitudinal observational study 100 RA patients were followed for anti-CCP2 IgG antibody (U/L) and total IgG level (mg/dL) every 6 months for a total period of 2.5 years. All patients received stable DMARD treatment during this period. Five groups comprising each 20 patients were analysed: (1) methotrexate (MTX) alone, (2) tumor necrosis factor inhibitors (TNFi), (3) tocilizumab (TCZ), (4) rituximab (RTX) and (5) abatacept (ABA). Results: Baseline demographic and disease-specific characteristics were comparable between the 5 groups. Anti-CCP2 antibody levels did not show significant changes in patients treated with MTX (mean±SEM: -24.1±8.1%), TNFi (-14.0±11.1%) or TCZ (-24.3±11.3%) between baseline and the 2, 5 years follow up. In contrast, anti-CCP2 antibody levels significantly decreased during treatment with RTX (-75.6±4.4%) and ABA (-82.5±3.7%). With respect to total IgG levels, no significant changes were observed with MTX (-24.1±8.1%), TNFi (-14.0±11.1%) or TCZ (-24.3±11.3%) over 2, 5 years. In contrast, anti-CCP2 antibody levels significantly decreased during treatment with RTX (-75.6±4.4%) and ABA (-82.5±3.7%). Date for individual patients are summarized in Figure 1. Conclusions: DMARDs targeting the adaptive immune response such as ABA and RTX significantly lowered anti-CCP2 IgG levels, while cytokine inhibitors and methotrexate had no significant effects on anti-CCP2 IgG levels. RTX is the only DMARD, which also lowers total IgG level. Lowering anti-CCP2 IgG levels is a step towards sero-conversion and immunological remission of disease. Disclosure of Interest: None declared … (more)
- Is Part Of:
- Annals of the rheumatic diseases. Volume 75(2016)Supplement 2
- Journal:
- Annals of the rheumatic diseases
- Issue:
- Volume 75(2016)Supplement 2
- Issue Display:
- Volume 75, Issue 2 (2016)
- Year:
- 2016
- Volume:
- 75
- Issue:
- 2
- Issue Sort Value:
- 2016-0075-0002-0000
- Page Start:
- 453
- Page End:
- 454
- Publication Date:
- 2016-07-15
- Subjects:
- Rheumatism -- Periodicals
616.723005 - Journal URLs:
- http://ard.bmjjournals.com/ ↗
http://www.pubmedcentral.nih.gov/tocrender.fcgi?journal=149&action=archive ↗
http://www.bmj.com/archive ↗
http://gateway.ovid.com/server3/ovidweb.cgi?T=JS&MODE=ovid&D=ovft&PAGE=titles&SEARCH=annals+of+the+rheumatic+diseases.tj&NEWS=N ↗ - DOI:
- 10.1136/annrheumdis-2016-eular.2454 ↗
- Languages:
- English
- ISSNs:
- 0003-4967
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
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- British Library DSC - BLDSS-3PM
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