| Literature DB >> 30459097 |
Nicolás Molano-González1, Manuel Rojas2, Diana M Monsalve1, Yovana Pacheco1, Yeny Acosta-Ampudia1, Yhojan Rodríguez1, Monica Rodríguez-Jimenez1, Carolina Ramírez-Santana1, Juan-Manuel Anaya3.
Abstract
Autoimmune diseases (ADs) are a chronic and clinically heterogeneous group of diseases characterized by share common immunopathogenic mechanisms and risk factors (i.e., the autoimmune tautology), which explain the fact that one AD may coexist with others (i.e., polyautoimmunity - PolyA). In the present exploratory study, a mixed-cluster analysis of the most common autoimmune rheumatic diseases (ARDs) was done. A total of 187 consecutive women with established systemic lupus erythematosus (n = 70), rheumatoid arthritis (n = 51), systemic sclerosis (n = 35) and Sjögren's syndrome (n = 31) were included. A comprehensive clinical, autoantibody and cytokine assessment was simultaneously done. Total PolyA was registered in 142 (75.9%) patients. Six clusters were obtained, built mainly on autoantibodies: PolyA-I to -VI. The PolyA-III cluster showed the highest frequency of overt PolyA (p = 0.01), and the PolyA-I, -III, and -IV clusters exhibited the highest positivity for IL-12/23p40 (p = 0.015). These results provide new insights into the pathophysiology of PolyA and warrant prospective validation to enable development of a more accurate taxonomy of ARDs.Entities:
Keywords: Interleukin-12/23p40; Rheumatoid arthritis; Sjögren's syndrome; Systemic lupus erythematosus; Systemic sclerosis; Taxonomy
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Year: 2018 PMID: 30459097 DOI: 10.1016/j.jaut.2018.11.002
Source DB: PubMed Journal: J Autoimmun ISSN: 0896-8411 Impact factor: 7.094