# The Use of Artificial Intelligence in Improving Diagnostic Modalities in Rheumatoid Arthritis: A Narrative Review

**Authors:** Sara Tariq, Arshia Ahmed, Gurdeep Singh, Paul Dura

PMC · DOI: 10.7759/cureus.102992 · 2026-02-04

## TL;DR

This paper reviews how artificial intelligence improves the diagnosis of rheumatoid arthritis by enhancing accuracy and enabling early detection.

## Contribution

The paper highlights novel AI-based algorithms that surpass traditional diagnostic methods in rheumatoid arthritis.

## Key findings

- AI models improve diagnostic accuracy by identifying early disease patterns and enhancing imaging characteristics.
- ML-integrated microRNA profiling outperforms traditional risk scoring models like RF and CCP in predicting joint deterioration.

## Abstract

Rheumatoid arthritis (RA) is an inflammatory autoimmune condition affecting the joints and other organs such as the heart, eyes, and lungs. For decades, it has been diagnosed through assessing a combination of clinical picture, serologic biomarkers, and radiographic studies. However, the possibility of false negative test results and inability to detect early arthritic changes make RA diagnosis challenging. The diagnostic accuracy of the RA diagnostic modalities has substantially improved since the emergence of artificial intelligence (AI)-based medical algorithms, resulting in timely disease prediction and prevention of irreversible joint damage. AI computational models employ machine learning (ML), natural language processing (NLP), and rule-based expert systems to enhance the diagnostic accuracy of rheumatological diseases, particularly rheumatoid arthritis. AI-based algorithms not only identify specific disease patterns to predict the early course of disease but also use visual scoring systems, enhancing imaging characteristics. Radiological studies such as X-ray, MRI, CT, and PET scan can quantify joint space narrowing, cartilage loss, synovitis, bone erosions, and bone marrow edema. In addition, ML-integrated microRNA gene profiling reshaped the microenvironment of joint space by modulating gene expression and reducing joint deterioration in rheumatoid arthritis patients, surpassing the rheumatoid factor (RF) and cyclic citrullinated peptide (CCP) risk scoring models.

## Linked entities

- **Diseases:** rheumatoid arthritis (MONDO:0008383)

## Full-text entities

- **Genes:** MIR155 (microRNA 155) [NCBI Gene 406947] {aka MIRN155, miRNA155, mir-155}, FAP (fibroblast activation protein alpha) [NCBI Gene 2191] {aka DPPIV, FAPA, FAPalpha, SIMP}, MUC1 (mucin 1, cell surface associated) [NCBI Gene 4582] {aka ADMCKD, ADMCKD1, ADTKD2, CA 15-3, CD227, Ca15-3}, MIR126 (microRNA 126) [NCBI Gene 406913] {aka MIRN126, miRNA126, mir-126}, MIR146A (microRNA 146a) [NCBI Gene 406938] {aka MIRN146, MIRN146A, miR-146a, miRNA146A}, ITGAV (integrin subunit alpha V) [NCBI Gene 3685] {aka CD51, IDNDC, MSK8, VNRA, VTNR}
- **Diseases:** autoimmune disease (MESH:D001327), functional (MESH:D003291), ML (MESH:D007859), ankylosis (MESH:D000844), osteoarthritis (MESH:D010003), arthritic (MESH:D015535), cartilage damage (MESH:D002357), scleroderma (MESH:D012595), vasculitis (MESH:D014657), inflammation (MESH:D007249), lung fibrosis (MESH:D005355), painful (MESH:D010146), quality (MESH:D012893), Parkinson's disease (MESH:D010300), microangiopathy (MESH:D014652), cancer (MESH:D009369), BME (MESH:D004487), ILD (MESH:D017563), arthritis (MESH:D001168), RA disease (MESH:D001172), Synovitis (MESH:D013585), bone erosions (MESH:D014077), RF (MESH:D001171), joint damage (MESH:D007592), Rheumatological diseases (MESH:D012216)
- **Chemicals:** fluorine-18 (MESH:C000615276), NaF (MESH:D012969), CCP (MESH:C487763), [18F]AlF-FAPI (-), RGD (MESH:C047981), 18F] fluorodeoxyglucose (MESH:D019788)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12965850/full.md

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Source: https://tomesphere.com/paper/PMC12965850