# Differential impacts of interstitial lung disease and airway disease on rheumatoid arthritis disease activity and infection

**Authors:** Misaki Yoshida, Midori Ueno, Takeshi Zoshima, Dai Inoue, Ichiro Mizushima, Satoshi Watanabe, Seiji Yano, Hideki Nomura, Mitsuhiro Kawano

PMC · DOI: 10.1038/s41598-025-23080-1 · 2025-11-13

## TL;DR

This study examines how lung and airway diseases affect rheumatoid arthritis activity and infection risks differently.

## Contribution

The study distinguishes the individual impacts of interstitial lung disease and airway disease on rheumatoid arthritis outcomes.

## Key findings

- RA disease activity was higher in patients with interstitial lung disease or airway disease.
- Interstitial lung disease was independently associated with increased infection risk after 50 months.
- Airway disease also increased infection risk, but not as strongly as interstitial lung disease.

## Abstract

We aimed to distinguish the individual effects of interstitial lung disease (ILD) and airway disease (AD) on rheumatoid arthritis (RA) disease activity and infection. RA patients who underwent chest CT at Kanazawa University Hospital (2011–2021) were investigated. The primary outcome was infection-related hospitalization, and the secondary was RA disease activity (DAS28-CRP, SDAI) at final observation. Of 569 patients, 125 (22.0%) had ILD (ILD +), and 171 (30.1%) had AD (AD +). At first CT: RA disease activity was similar; ILD + received less methotrexate than ILD–; all DMARDs were similar in AD + and AD–. At final observation (mean: 73.9 months): RA disease activity was higher in ILD + and AD + . Analysis of covariance revealed a significant association between final RA disease activity and ILD, but not AD. Kaplan–Meier analysis showed lower infection-free rates in ILD + and AD + . Cox regression analysis with time-dependent covariates showed an association between infection and ILD after 50 months and AD (HR 3.702 and 1.744). RA disease activity was independently associated with ILD, likely due to reduced methotrexate use. ILD after 50 months and AD both increased infection risk independently. Distinguishing ILD from AD is important for selecting safe and effective treatments.

The online version contains supplementary material available at 10.1038/s41598-025-23080-1.

## Linked entities

- **Diseases:** rheumatoid arthritis (MONDO:0008383), interstitial lung disease (MONDO:0015925)

## Full-text entities

- **Genes:** CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}
- **Diseases:** RA disease (MESH:D001172), AD (MESH:D029424), ILD (MESH:D017563), infection (MESH:D007239)
- **Chemicals:** methotrexate (MESH:D008727)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12615712/full.md

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Source: https://tomesphere.com/paper/PMC12615712