Machine learning for screening and predicting the risk of anti-MDA5 antibody in juvenile dermatomyositis children

Front Immunol. 2023 Jan 10:13:940802. doi: 10.3389/fimmu.2022.940802. eCollection 2022.

Abstract

Objective: The anti-MDA5 (anti-melanoma differentiation associated gene 5) antibody is often associated with a poor prognosis in juvenile dermatomyositis (JDM) patients. In many developing countries, there is limited ability to access myositis- specific antibodies due to financial and technological issues, especially in remote regions. This study was performed to develop a prediction model for screening anti-MDA5 antibodies in JDM patients with commonly available clinical findings.

Methods: A cross-sectional study was undertaken with 152 patients enrolled from the inpatient wards of Beijing Children's Hospital between June 2018 and September 2021. Stepwise logistic regression, least absolute shrinkage and selection operator (LASSO) regression, and the random forest (RF) method were used to fit the model. Model discrimination, calibration, and decision curve analysis were performed for validation.

Results: The final prediction model included eight clinical variables (gender, fever, alopecia, periungual telangiectasia, digital ulcer, interstitial lung disease, arthritis/arthralgia, and Gottron sign) and four auxiliary results (WBC, CK, CKMB, and ALB). An anti-MDA5 antibody risk probability-predictive nomogram was established with an AUC of 0.975 predicted by the random forest algorithm. The model was internally validated by Harrell's concordance index (0.904), the Brier score (0.052), and a 500 bootstrapped satisfactory calibration curve. According to the net benefit and predicted probability thresholds of decision curve analysis, the established model showed a significantly higher net benefit than the traditional logistic regression model.

Conclusion: We developed a prediction model using routine clinical assessments to screen for JDM patients likely to be anti-MDA5 positive. This new tool may effectively predict the detection of anti-MDA5 in these patients using a non-invasive and efficient way.

Keywords: antiMDA5; antibody; juvenile dermatomyositis; machine learning; pediatric.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antibodies
  • Child
  • Cross-Sectional Studies
  • Dermatomyositis*
  • Humans
  • Interferon-Induced Helicase, IFIH1
  • Machine Learning
  • Risk Factors

Substances

  • Interferon-Induced Helicase, IFIH1
  • Antibodies

Supplementary concepts

  • digital ulcers

Grants and funding

This work was supported by the Capital’s Funds for Health Improvement and Research (CFH2018-2-2093).