Inflammatory myopathies

Urinary β2-microglobulin as a prognostic and treatment-associated biomarker in anti-MDA5 antibody-positive DM with interstitial lung disease

Rheumatology (Oxford)Published retrospective, single-center design

Authors' conclusion

U-β2M is a promising, non-invasive prognostic and treatment-associated marker for MDA5-DM with ILD, showing more pronounced longitudinal change than serum ferritin and KL-6. However, given the retrospective, single-center design of this study, prospective validation in larger cohorts is warranted.

Study context

Population
Patients with anti-MDA5 antibody-positive dermatomyositis (MDA5-DM) with interstitial lung disease (ILD) admitted between January 2004 and March 2023baseline U-β2M available (16 deaths, 36 survivors), 63 patients included (20 deaths, 43 survivors) of 68 identified · included 63 · baseline U-β2M available 52
Participants
52 patientsEvents: 16
Predictors
Urinary β2-microglobulin (U-β2M); serum ferritin, anti-MDA5 antibody titres and serum Krebs von den Lungen-6 (KL-6) compared
Predicted outcome
mortality

Model performance

As reported in the abstract

Area under the curve
U-β2M
0.72
Serum ferritin
0.68
anti-MDA5 antibody titres
0.69
KL-6
0.50
  • U-β2M comparable to serum ferritin and anti-MDA5 antibody titres
  • U-β2M vs KL-6: P = 0.0394

Further findings

U-β2M levels at admission, deceased vs survivors

Significantly higher in the deceased group
P = 0.011

Correlation of U-β2M with anti-MDA5 antibody titres and serum ferritin

Correlation with anti-MDA5 antibody titres
P < 0.0001
Correlation with serum ferritin
P < 0.0001

Post-treatment change in U-β2M, serum ferritin and KL-6

U-β2M decreased in survivors
P = 0.009
U-β2M increased in deceased patients
P = 0.009
Serum ferritin did not change significantly, survivors
P = 0.086
Serum ferritin did not change significantly, deceased
P = 0.782
KL-6 did not change significantly in survivors
P = 0.059
KL-6 increased in the deceased group
P < 0.0001

Original publication

Urinary β2-microglobulin as a prognostic and treatment-associated biomarker in anti-MDA5 antibody-positive DM with interstitial lung disease. Rheumatology (Oxford). Published 13 November 2026. doi:10.1093/rheumatology/keag632

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