Pediatric rheumatology

Clinical Features and Immunogenetic Risk Factors Associated With Additional Autoantibodies in Anti‐Transcriptional Intermediary Factor 1γ Juvenile‐Onset Dermatomyositis

Arthritis RheumatolPublished Cross-sectional study

Authors' conclusion

Autoantibodies associated with anti-TIF1γ were found in isolation and in combination among a subset of patients with JDM. Patients with these autoantibodies had less severe muscle disease and were not enriched for HLA-DRB1*03.

Study context

Population
Patients with anti-TIF1γ autoantibody-positive JDM and juvenile healthy controlsplus 90 healthy controls
Participants
150 patients
Exposure
Anti-TIF1γ JDM with vs without anti-TIF1γ-associated autoantibodies
  • Any associated autoantibodyn = 44
  • Healthy controlsn = 90
Outcome
Prevalence of anti-CCAR1, anti-C1Z1, anti-IMMT, anti-TBL1XR1 and anti-Sp4 autoantibodies and their associated features

Main finding

As reported in the abstract

Prevalence of anti-TIF1γ-associated autoantibodies in anti-TIF1γ JDM
Any anti-TIF1γ-associated autoantibody
44 (29%)
Anti-Sp4
25 (17%)
Anti-TBL1XR1
22 (15%)
Anti-CCAR1
14 (9%)
Anti-C1Z1
2 (1%)
Anti-IMMT
2 (1%)

Observational data: associations, not effects.

Further findings

OutcomeAny associated autoantibodyWithout associated autoantibodiesP value
FallingAny associated autoantibody vs Without associated autoantibodies34%53%P = 0.032

Falling

Lower peak muscle enzymes with any associated autoantibody

Cancer

None of the patients had cancer
0

HLA-DRB1*03 and any anti-TIF1γ-associated autoantibody (White patients)

OR (protective)
0.20 (95% CI 0.07-0.52)

Original publication

Clinical Features and Immunogenetic Risk Factors Associated With Additional Autoantibodies in Anti‐Transcriptional Intermediary Factor 1γ Juvenile‐Onset Dermatomyositis. Arthritis Rheumatol. Published 30 January 2024. doi:10.1002/art.42768

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