Inflammatory myopathies

Cessation of Immunomodulatory Medication Use in Dermatomyositis: A Single‐Center Cohort Study

Arthritis Care Res (Hoboken)Published Retrospective cohort study

Authors' conclusion

Approximately 20% of adult DM patients discontinued immunomodulatory medications over a median 7-year follow-up. Those with clinically amyopathic disease, anti-MDA5, anti-NXP2, and anti-SAE1 antibodies have a higher likelihood of medication cessation.

Study context

Population
Adult dermatomyositis (DM) patients seen in a rheumatology/dermatology clinic, 2013–2020, exposed to ≥1 systemic immunomodulatory medication for ≥3 monthsmedian follow-up ∼7 years
Participants
246 participants
Exposure
Clinical and autoantibody subgroups of adult DM, for discontinuation of systemic immunomodulatory therapy
Outcome
Discontinuation of all immunomodulatory medications for at least 12 months
Methodological detailssingle-centre, Kaplan-Meier with log-rank analyses, Cox proportional hazards models
  • Single-centre
  • Kaplan-Meier with log-rank analyses
  • Cox proportional hazards models

Main finding

As reported in the abstract

Discontinued all immunomodulatory medications

All DM patients

19%

47 events

Observational data: associations, not effects.

Further findings

OutcomeHR (95% CI)
Medication cessation by autoantibody (multivariate)Anti-MDA5vs Autoantibody-negative9.83 (2.00–48.2)
Medication cessation by autoantibody (multivariate)Anti-NXP2vs Autoantibody-negative8.92 (1.69–47.0)
Medication cessation by autoantibody (multivariate)Anti-SAE1vs Autoantibody-negative10.8 (2.06–56.6)
OutcomeFold more likely (95% CI)P value
Medication cessation by clinical phenotype (multivariate)Clinically amyopathic vs Muscle disease2.7 (1.34–5.59)
Time to medication discontinuation (log-rank)Anti-MDA5 vs Autoantibody-negative · anti-MDA5 discontinued medications fasterP = 0.03

Original publication

Cessation of Immunomodulatory Medication Use in Dermatomyositis: A Single‐Center Cohort Study. Arthritis Care Res (Hoboken). Published 18 January 2023. doi:10.1002/acr.24980

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