Anti-carbamylated protein antibodies positivity and disease activity in Hispanic patients with established rheumatoid arthritis: An observational study

Author:

Vega-Morales David1ORCID,Garza-Elizondo Mario A1ORCID,Trouw Leendert A2ORCID,Gonzalez-Torres Karina I1,Torres-Lopez Ernesto3ORCID,Eguia-Bernal Miryam1,Loredo-Alanis Salvador A1,Gracia-Arechiga Tayde S1ORCID,Vazquez-Fuentes Brenda R1,Castañeda-Martinez Diana D1,Castañeda-Martinez Martha M1ORCID,Elizondo-Solis Cesar V1ORCID,Mendiola-Jimenez Andres1,Salinas-Carmona Mario C3ORCID,Herrera-Sandate Pablo1ORCID,la Garza Jesus A Cardenas-de1ORCID,Rodriguez-Sanchez Gerardo E1,Galarza-Delgado Dionicio A1ORCID

Affiliation:

1. Rheumatology Service and Internal Medicine Department, Hospital Universitario “Dr. José Eleuterio González”, Universidad Autónoma de Nuevo León, Monterrey, Mexico

2. Department of Immunohematology and Bloodtransfusion, Leiden University Medical Center, Leiden, The Netherlands

3. Immunology Department, Hospital Universitario “Dr. José Eleuterio González”, Universidad Autónoma de Nuevo León, Monterrey, Mexico

Abstract

Abstract Objectives We aimed to determine the prevalence of anti-carbamylated protein (anti-CarP) antibodies in Mexican Hispanics with established rheumatoid arthritis (RA) and to assess their relationship with disease activity. Methods A cohort study was conducted in 278 patients with established RA during an 18-month follow-up. We measured IgG/IgM/IgA rheumatoid factor (RF), IgG anticitrullinated protein antibodies (ACPA) and IgG/IgM/IgA anti-CarP antibodies using enzyme-linked immunosorbent assay (ELISA). For disease activity, we performed the 28-joint disease activity score with erythrocyte sedimentation rate (DAS28-ESR). Repeated measures one-way ANOVA was used to test the association between anti-CarP IgG antibody status and longitudinal DAS28-ESR scores. Patients were evaluated at baseline and at 6, 12, and 18 months during follow-up. Results Anti-CarP IgG antibodies were positive in 47.8% of patients and, accounting for all isotypes, in 9.5% of patients with negative RF and ACPA. Triple antibody positivity was present in 42.6% of patients in our sample. Anti-CarP IgG antibody positivity did not show statistically significant differences in mean DAS28-ESR when compared to anti-CarP IgG antibody negative patients at baseline, 6, 12 or 18 months. Conclusion Anti-CarP IgG antibodies are not associated to a higher disease activity in Hispanic patients with established RA. Our findings suggest that the clinical value of measuring anti-CarP antibodies in RA diminishes over time.

Funder

UCB

Publisher

Oxford University Press (OUP)

Subject

Rheumatology

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