# A DNA methylation-based algorithm for diagnosing rheumatoid arthritis

**Authors:** Espen Riskedal, Astanand Jugessur, Silje Watterdal Syversen, Cathrine Lund Hadley, Jennifer R. Harris, Maria Dahl Mjaavatten, Joe Sexton, Janis Neumann, Gina Hetland Brinkmann, Guro Løvik Goll, Grethe-Elisabeth Stenvik, Håkon Bøås, Arne Søraas, Karl Trygve Kalleberg, Siri Lillegraven, Espen A. Haavardsholm

PMC · DOI: 10.1186/s13075-025-03649-x · Arthritis Research & Therapy · 2025-10-17

## TL;DR

This study developed a DNA methylation-based algorithm that can help diagnose rheumatoid arthritis, especially in cases where traditional blood tests are inconclusive.

## Contribution

A novel DNA methylation-based algorithm for early RA diagnosis, particularly effective for seronegative cases.

## Key findings

- The algorithm achieved high sensitivity and specificity in distinguishing RA from controls when combined with serological status.
- It performed well in identifying seronegative RA patients, who are typically harder to diagnose.
- The algorithm used 391 DNA methylation features to classify RA cases effectively.

## Abstract

Rheumatoid arthritis (RA), particularly seronegative disease, is difficult to diagnose early, which can delay treatment initiation. This study aims to develop a binary DNA methylation (DNAm)-based algorithm to diagnose RA.

Three datasets (discovery, training, holdout) were constructed from DNAm profiles from 1366 persons (treatment-naïve RA, other inflammatory/autoimmune diseases, healthy individuals). DNAm features that differentiate RA from other inflammatory/autoimmune diseases and healthy individuals were identified using the discovery set. Our classification algorithm was developed using machine learning techniques in the training set. Its diagnostic performance, with and without serological status, was evaluated in the holdout set containing RA cases (15 seropositive, 6 seronegative) and controls (14 other arthritides, 11 healthy individuals).

Our algorithm included 391 DNAm features. Combined with serological status, it classified RA from controls in the holdout set with the following performance: sensitivity 0.90 [95% CI: 0.70–0.99], specificity 0.88 [95% CI: 0.69–0.97], and AUC 0.96 [95% CI: 0.91–1.00]. Its performance in classifying patients with seronegative RA versus those with other arthritides was: sensitivity 0.83 [95% CI: 0.36–1.00], specificity 0.79 [95% CI: 0.49–0.95], and AUC 0.81 [95% CI: 0.61–1.00].

The present DNAm-based classification algorithm may be clinically useful for the early diagnosis of RA, especially in seronegative patients, which currently often poses a diagnostic challenge.

The online version contains supplementary material available at 10.1186/s13075-025-03649-x.

## Linked entities

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

## Full-text entities

- **Diseases:** RA (MESH:D001172), seronegative disease (MESH:D004194), inflammatory/autoimmune diseases (MESH:D001327), arthritides (MESH:D001168)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12532955/full.md

## References

2 references — full list in the complete paper: https://tomesphere.com/paper/PMC12532955/full.md

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Source: https://tomesphere.com/paper/PMC12532955