The long-term association between mRNA-based coronavirus disease 2019 (COVID-19) vaccination and the development of autoimmune connective tissue diseases (AI-CTDs) remains unclear. In this nationwide, population-based cohort study involving 9,258,803 individuals, we aim to determine whether the incidence of AI-CTDs is associated with mRNA vaccination. The study spans over 1 year of observation and further analyses the risk of AI-CTDs by stratifying demographics and vaccination profiles and treating booster vaccination as time-varying covariate. We report that the risk of developing most AI-CTDs did not increase following mRNA vaccination, except for systemic lupus erythematosus with a 1.16-fold risk in vaccinated individuals relative to controls. Comparable results were reported in the stratified analyses for age, sex, mRNA vaccine type, and prior history of non-mRNA vaccination. However, a booster vaccination was associated with an increased risk of some AI-CTDs including alopecia areata, psoriasis, and rheumatoid arthritis. Overall, we conclude that mRNA-based vaccinations are not associated with an increased risk of most AI-CTDs, although further research is needed regarding its potential association with certain conditions.
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http://dx.doi.org/10.1038/s41467-024-50656-8 | DOI Listing |
Nat Commun
July 2024
Department of Dermatology, Yonsei University Wonju College of Medicine, Wonju, Republic of Korea.
Ann Rheum Dis
October 2018
Leeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds, Chapel Allerton Hospital, Leeds, UK.
Objective: To evaluate clinical, interferon and imaging predictors of progression from 'At Risk' to autoimmune connective tissue diseases (AI-CTDs).
Methods: A prospective observational study was conducted in At-Risk of AI-CTD (defined as antinuclear antibody (ANA) positive; ≤1 clinical systemic lupus erythematosus (SLE) criterion; symptom duration <12 months and treatment-naïve). Bloods and skin biopsy (non-lesional) were analysed for two interferon-stimulated gene expression scores previously described (IFN-Score-A and IFN-Score-B).
J Long Term Eff Med Implants
April 2003
International Epidemiology Institute, Rockville, Maryland 20850, USA.
Because implants can provoke varied immune system responses, we assessed whether hip and knee implant recipients had an increased risk of autoimmune/connective tissue diseases (AI/CTDs). Using national registry data from Sweden, we compared hospitalization rates for AI/CTD in 101,771 hip and 23,891 knee implant recipients to rates in the general population. Hip patients were followed up to 22 years and knee patients up to 14 years postimplantation.
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