Circulating anti‐citrullinated protein antibodies containing secretory component are prognostic for arthritis onset in at‐risk patients
Autor: | Anna Svärd, Jonas Wetterö, Alf Kastbom, Klara Martinsson, K Roos Ljungberg |
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Jazyk: | angličtina |
Rok vydání: | 2021 |
Předmět: |
0301 basic medicine
rheumatoid arthritis Male Arthritis Anti-Citrullinated Protein Antibodies Arthritis Rheumatoid 0302 clinical medicine immune system diseases secretory component Immunology and Allergy Longitudinal Studies Prospective Studies skin and connective tissue diseases mucosa biology Hazard ratio Anti–citrullinated protein antibody Middle Aged Prognosis Isotype Immunoglobulin Isotypes at-risk patients Rheumatoid arthritis Original Article Female Antibody musculoskeletal diseases Immunology Gastroenterology and Hepatology 03 medical and health sciences Rheumatoid Factor medicine Gastroenterologi at‐risk patients Humans anti-citrullinated protein antibodies Rheumatology and Autoimmunity Autoantibodies Reumatologi och inflammation business.industry Proportional hazards model Autoantibody anti‐citrullinated protein antibodies Original Articles medicine.disease Autoimmunity/Autoimmune diseases Secretory Component 030104 developmental biology biology.protein business 030215 immunology |
Zdroj: | Clinical and Experimental Immunology |
ISSN: | 1365-2249 0009-9104 |
Popis: | Summary Autoantibodies related to rheumatoid arthritis (RA), such as anti‐citrullinated protein antibodies (ACPA), are often detectable in the preclinical period years before arthritis onset. However, events triggering arthritis development remain incompletely known. We aimed to determine whether ACPA isotype levels are prognostic for arthritis development in patients presenting with immunoglobulin (Ig)G ACPA and musculoskeletal pain. Study participants (n = 82) had musculoskeletal pain of any sort and duration and a positive IgG ACPA test. None of the patients had arthritis upon clinical examination at baseline, but during follow‐up (mean = 6 years), 48% developed at least one arthritic joint. IgG, IgA, IgM and secretory component (SC)‐containing ACPA was measured in longitudinally collected serum samples. Cox regression analysis was performed to test the prognostic value of baseline antibody levels and changes over time. All analysed ACPA isotype levels were associated with arthritis development in univariable Cox regression analysis. In multivariable analysis, baseline SC ACPA levels were independently prognostic for arthritis development in multivariable analysis [hazard ratio (HR) = 1·006, 95% confidence interval (CI) = 1·001–1·010, P = 0·012]. There were no significant changes in ACPA isotype levels over time, and no significant association between changes over time and arthritis development. In this prospective longitudinal study, baseline serum SC ACPA levels, but neither IgG, IgA nor IgM ACPA are prognostic for future arthritis development. Repeated measurement of ACPA isotypes do not bring additional prognostic value. The results reinforce a mucosal connection in RA development and encourage further exploration of the mechanisms underlying secretory ACPA formation as a trigger for arthritis development. Smoking habits in relation to different anti‐citrullinated protein antibody (ACPA) isotypes (IgG, IgA, IgM and SC) in TIRx patients. *p‐value |
Databáze: | OpenAIRE |
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