Predicting Rheumatoid Arthritis Development Using Hand Ultrasound and Machine Learning—A Two-Year Follow-Up Cohort Study

Author:

Daskareh Mahyar1ORCID,Vakilpour Azin2,Barzegar-Golmoghani Erfan3,Esmaeilian Saeid4ORCID,Gilanchi Samira5,Ezzati Fatemeh6,Alikhani Majid7,Rahmanipour Elham8,Amini Niloofar7,Ghorbani Mohammad9ORCID,Pezeshk Parham10ORCID

Affiliation:

1. Department of Radiology, University of California San Diego, San Diego, CA 92093, USA

2. Division of Cardiovascular Diseases, Department of Medicine, Hospital of the University of Pennsylvania, Philadelphia, PA 19104, USA

3. Department of Biomedical Engineering, Tarbiat Modares University, Tehran 14115-111, Iran

4. Department of Radiology, Shiraz University of Medical Sciences, Shiraz 71348, Iran

5. Proteomics Research Center, Shahid Beheshti University of Medical Sciences, Tehran 19839-63113, Iran

6. Division of Rheumatic Disease, Department of Internal Medicine, UT Southwestern Medical Center, Dallas, TX 75390, USA

7. Department of Internal Medicine, Rheumatology Research Center, Shariati Hospital, Tehran University of Medical Sciences, Tehran 14117-13135, Iran

8. Immunology Research Center, Mashhad University of Medical Sciences, Mashhad 91779-48564, Iran

9. Orthopedic Research Center, Mashhad University of Medical Sciences, Mashhad 91779-48564, Iran

10. Division of Musculoskeletal Imaging, Department of Radiology, UT Southwestern Medical Center, Dallas, TX 75390, USA

Abstract

Background: The early diagnosis and treatment of rheumatoid arthritis (RA) are essential to prevent joint damage and enhance patient outcomes. Diagnosing RA in its early stages is challenging due to the nonspecific and variable clinical signs and symptoms. Our study aimed to identify the most predictive features of hand ultrasound (US) for RA development and assess the performance of machine learning models in diagnosing preclinical RA. Methods: We conducted a prospective cohort study with 326 adults who had experienced hand joint pain for less than 12 months and no clinical arthritis. We assessed the participants clinically and via hand US at baseline and followed them for 24 months. Clinical progression to RA was defined according to the ACR/EULAR criteria. Regression modeling and machine learning approaches were used to analyze the predictive US features. Results: Of the 326 participants (45.10 ± 11.37 years/83% female), 123 (37.7%) developed clinical RA during follow-up. At baseline, 84.6% of the progressors had US synovitis, whereas 16.3% of the non-progressors did (p < 0.0001). Only 5.7% of the progressors had positive PD. Multivariate analysis revealed that the radiocarpal synovial thickness (OR = 39.8), PIP/MCP synovitis (OR = 68 and 39), and wrist effusion (OR = 12.56) on US significantly increased the odds of developing RA. ML confirmed these US features, along with the RF and anti-CCP levels, as the most important predictors of RA. Conclusions: Hand US can identify preclinical synovitis and determine the RA risk. The radiocarpal synovial thickness, PIP/MCP synovitis, wrist effusion, and RF and anti-CCP levels are associated with RA development.

Publisher

MDPI AG

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