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Predicting anti-TNF treatment response in rheumatoid arthritis: An artificial intelligence-driven model using
Juan Luis Valdivieso Shephard1, Enrique Josue Alvarez Robles2, Carmen Cámara Hijón3
1Immunology Unit, Hospital Universitario La Paz-Idipaz, 28046, Madrid, Spain.
Introduction:
Rheumatoid arthritis (RA) is a heterogeneous disease in which therapeutic strategies used have evolved dramatically. Despite significant progress in treatment strategies such as the development of anti-TNF drugs, it is still not possible to differentiate those patients who will respond from who will not. This can lead to effective-treatment delays and unnecessary costs. The aim of this study was to utilize a profile of the patient's characteristics, clinical parameters, immune status (cytokine profile) and artificial intelligence to assess the feasibility of developing a tool that could allow us to predict which patients will respond to treatment with anti-TNF drugs.
Methods:
This study included 38 patients with RA from the RA-Paz cohort. Clinical activity was measured at baseline and after 6 months of treatment. The cytokines measured before the start of anti-TNF treatment were IL-1, IL-12, IL-10, IL-2, IL-4, IFNg, TNFa, and IL-6. Statistical analyses were performed using the Wilcoxon-Rank-Sum Test and the Benjamini-Hochberg method. The predictive model viability was explored using the 5-fold cross-validation scheme in order to train the logistic regression models.
Results:
Statistically significant differences were found in parameters such as IL-6, IL-2, CRP and DAS-ESR. The predictive model performed to an acceptable level in correctly classifying patients (ROC-AUC 0.804167 to 0.891667), suggesting that it would be possible to develop a clinical classification tool.
Conclusions:
Using a combination of parameters such as IL-6, IL-2, CRP and DAS-ESR, it was possible to develop a predictive model that can acceptably discriminate between remitters and non-remitters. However, this model needs to be replicated in a larger cohort to confirm these findings.
Insights
Researchers developed a predictive model using cytokines like IL-6 and IL-2 to identify rheumatoid arthritis (RA) patients likely to respond to anti-TNF drugs, improving treatment selection.
Area of Science:
- Immunology
- Rheumatology
- Artificial Intelligence in Medicine
Background:
- Rheumatoid arthritis (RA) treatment response varies significantly among patients.
- Current anti-tumor necrosis factor (anti-TNF) therapies lack predictive markers for individual patient response.
- This variability leads to treatment delays and increased healthcare costs.
Purpose of the Study:
- To assess the feasibility of developing a predictive tool for anti-TNF therapy response in RA patients.
- To utilize patient characteristics, clinical parameters, and cytokine profiles with artificial intelligence.
Main Methods:
- Analysis of 38 RA patients from the RA-Paz cohort.
- Measurement of baseline cytokine profiles (IL-1, IL-12, IL-10, IL-2, IL-4, IFNg, TNFa, IL-6) and clinical parameters (CRP, DAS-ESR).
- Development and validation of logistic regression models using 5-fold cross-validation.
Main Results:
- Statistically significant differences observed in IL-6, IL-2, CRP, and DAS-ESR between responders and non-responders.
- The predictive model demonstrated acceptable performance with a ROC-AUC range of 0.804167 to 0.891667.
- The findings suggest the potential for a clinical classification tool.
Conclusions:
- A predictive model combining IL-6, IL-2, CRP, and DAS-ESR can effectively discriminate between RA patients who will remit and those who will not respond to anti-TNF therapy.
- Further validation in larger cohorts is necessary to confirm these promising findings.
- This approach could personalize RA treatment strategies.
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