ATRPred: A machine learning based tool for clinical decision making of anti-TNF treatment in rheumatoid arthritis

Bodhayan Prasad1, Cathy McGeough1, Amanda Eakin1

  • 1Northern Ireland Centre for Stratified Medicine (NICSM), Biomedical Sciences Research Institute, Ulster University, C-TRIC Building, Altnagelvin Area Hospital, Londonderry, United Kingdom.

Insights

Researchers developed ATRPred, a machine learning tool to predict anti-tumour necrosis factor (anti-TNF) therapy response in rheumatoid arthritis (RA) patients. This predictor identifies individuals likely to benefit, improving treatment outcomes and reducing costs.

Area of Science:

  • Immunology
  • Biochemistry
  • Computational Biology

Background:

  • Rheumatoid arthritis (RA) is a chronic autoimmune disease causing joint pain and disability.
  • Targeted biologic treatments, like anti-tumour necrosis factor (anti-TNF) therapy, are effective but expensive, and not all patients respond.
  • Identifying non-responders early can prevent disease refractoriness and improve patient quality of life.

Purpose of the Study:

  • To identify predictive biomarkers for anti-TNF therapy response in RA patients.
  • To develop a machine learning model for predicting treatment outcomes.
  • To aid clinicians in personalizing anti-TNF therapy selection.

Main Methods:

  • Plasma samples from 144 RA patients commencing anti-TNF therapy were analyzed using Olink's proximity extension assays for 368 proteins.
  • Machine learning with 5-fold nested cross-validation was applied to identify proteins associated with treatment response.
  • A classifier, ATRPred, was developed based on 17 significantly associated proteins.

Main Results:

  • Preliminary analysis revealed two distinct molecular subgroups in RA patients, differing in gender and disease activity but not anti-TNF response.
  • The ATRPred classifier achieved 81% accuracy, 75% sensitivity, and 86% specificity in predicting anti-TNF treatment response.
  • Seventeen proteins were identified as significantly associated with treatment response.

Conclusions:

  • ATRPred offers a promising tool for predicting anti-TNF therapy response in RA patients.
  • This predictor can assist clinicians in optimizing treatment strategies, potentially reducing healthcare costs and improving patient outcomes.
  • Further validation is warranted to integrate ATRPred into clinical practice for personalized rheumatoid arthritis management.

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