In adult onset myositis, the presence of interstitial lung disease and myositis specific/associated antibodies are governed by HLA class II haplotype, rather than by myositis subtype
2005

HLA Class II Associations in Myositis

Sample size: 225 publication Evidence: high

Author Information

Author(s): Chinoy Hector, Salway Fiona, Fertig Noreen, Shephard Neil, Tait Brian D, Thomson Wendy, Isenberg David A, Oddis Chester V, Silman Alan J, Ollier William E, Cooper Robert G

Primary Institution: the UK Adult Onset Myositis Immunogenetic Collaboration (AOMIC)

Hypothesis

HLA class II associations differ between polymyositis and dermatomyositis.

Conclusion

The study found that different HLA class II haplotypes are associated with distinct myositis subtypes and their clinical features.

Supporting Evidence

  • HLA-DRB1*03, DQA1*05 and DQB1*02 were associated with increased risk for both PM and DM.
  • The HLA-DRB1*03-DQA1*05-DQB1*02 haplotype was strongly associated with ILD.
  • HLA-DRB1*07-DQA1*02-DQB1*02 haplotype was associated with risk for anti-Mi-2 antibodies.
  • There were no associations with malignancy.
  • Different HLA haplotypes influence clinical features in PM and DM.

Takeaway

This study looked at how certain genes affect two types of muscle diseases, showing that different genes are linked to different disease features.

Methodology

A cross-sectional, case-control study comparing HLA class II in cases of PM and DM with normal subjects.

Potential Biases

Multi-centre recruitment may have led to subtype misclassification.

Limitations

Potential misclassification of disease subtypes and underestimation of ILD and malignancy due to the study design.

Participant Demographics

225 UK Caucasian patients aged 18 and older, with 117 having polymyositis and 108 having dermatomyositis.

Statistical Information

P-Value

p = 0.0001

Confidence Interval

95% CI 0.1–0.6

Statistical Significance

p<0.05

Digital Object Identifier (DOI)

10.1186/ar1862

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