Risk factors of incident lung diseases and the impact of DMARDs in rheumatoid arthritis patients: a longitudinal study

We aimed to investigate the impact of clinical characteristics and therapy on rheumatoid arthritis (RA)-related lung diseases. The retrospective cohort consisted of 1,207 inpatients at baseline. RA-related lung diseases included interstitial lung disease (ILD), bronchiectasis, pleural effusion, and pulmonary arterial hypertension. Kaplan-Meier method was used to measure the cumulative incidence curve. Cox regression was conducted to evaluate the associations between RA-related lung diseases and risk indicators. Logistic regression was employed to examine the impact of drugs. The study identified 145 cases of RA-related lung diseases (34.2/1,000 person-years; 95% CI: 28.6–39.7) and 98 RA-ILD cases (22.5/1,000 person-years; 95% CI: 18.0–26.9) over 3.5 years. The cumulative incidence of RA-related lung diseases increased continuously over time, accelerating after 10 years of RA and age 55. RA-related lung diseases was independently associated with older age at RA onset (per 10 years, hazard ratio [HR] = 1.22, 95% confidence interval [CI]: 1.04–1.42), longer RA duration (per 10 years, HR = 1.43, 95% CI: 1.15–1.77), higher Rheumatic Disease Comorbidity Index (HR = 1.22, 95% CI: 1.08–1.39), prior pulmonary infections (HR = 2.26, 95% CI: 1.58–3.24), and systemic lupus erythematosus comorbidity (HR = 2.36, 95% CI: 1.35–4.13). After adjustment, ever-use of methotrexate demonstrated a significant protective association against both RA-related lung diseases (odds ratio [OR] = 0.64, 95% CI: 0.44–0.92) and RA-ILD (OR = 0.54, 95% CI: 0.35–0.83). Similarly, biologic or targeted synthetic disease modifying antirheumatic drugs (b/tsDMARDs) were also found protective (OR = 0.59, 95% CI: 0.35–0.99). This study identifies several clinically significant risk factors for RA-related lung diseases, while demonstrating protective effects of methotrexate and b/tsDMARDs.

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Journal
BMC Pulmonary Medicine
Published
2025-11-03
DOI
https://doi.org/10.1186/s12890-025-03915-3
Primary Topic
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
Type
article
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article

Risk factors of incident lung diseases and the impact of DMARDs in rheumatoid arthritis patients: a longitudinal study

Linyu Geng, Zhijie Qian, Guangcai Chen, Kexin Zhu et al.
BMC Pulmonary Medicine
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
article

Risk factors of incident lung diseases and the impact of DMARDs in rheumatoid arthritis patients: a longitudinal study

Linyu Geng, Zhijie Qian, Guangcai Chen, Kexin Zhu, Xiaojun Tang, Qing Shu, Xuebing Feng, Ziyi Jin, Hongwei Chen, Yaqi Zhang, Dandan Wang, Lingyun Sun, Jun Liang, Xinqi Xu, Qing Zhang, Huayong Zhang
article en

Abstract

We aimed to investigate the impact of clinical characteristics and therapy on rheumatoid arthritis (RA)-related lung diseases. The retrospective cohort consisted of 1,207 inpatients at baseline. RA-related lung diseases included interstitial lung disease (ILD), bronchiectasis, pleural effusion, and pulmonary arterial hypertension. Kaplan-Meier method was used to measure the cumulative incidence curve. Cox regression was conducted to evaluate the associations between RA-related lung diseases and risk indicators. Logistic regression was employed to examine the impact of drugs. The study identified 145 cases of RA-related lung diseases (34.2/1,000 person-years; 95% CI: 28.6–39.7) and 98 RA-ILD cases (22.5/1,000 person-years; 95% CI: 18.0–26.9) over 3.5 years. The cumulative incidence of RA-related lung diseases increased continuously over time, accelerating after 10 years of RA and age 55. RA-related lung diseases was independently associated with older age at RA onset (per 10 years, hazard ratio [HR] = 1.22, 95% confidence interval [CI]: 1.04–1.42), longer RA duration (per 10 years, HR = 1.43, 95% CI: 1.15–1.77), higher Rheumatic Disease Comorbidity Index (HR = 1.22, 95% CI: 1.08–1.39), prior pulmonary infections (HR = 2.26, 95% CI: 1.58–3.24), and systemic lupus erythematosus comorbidity (HR = 2.36, 95% CI: 1.35–4.13). After adjustment, ever-use of methotrexate demonstrated a significant protective association against both RA-related lung diseases (odds ratio [OR] = 0.64, 95% CI: 0.44–0.92) and RA-ILD (OR = 0.54, 95% CI: 0.35–0.83). Similarly, biologic or targeted synthetic disease modifying antirheumatic drugs (b/tsDMARDs) were also found protective (OR = 0.59, 95% CI: 0.35–0.99). This study identifies several clinically significant risk factors for RA-related lung diseases, while demonstrating protective effects of methotrexate and b/tsDMARDs.

BMC Pulmonary MedicineVol. 25(1)
Nanjing University of Chinese Medicine (CN), China Pharmaceutical University (CN), Nanjing Drum Tower Hospital (CN)
Government of Jiangsu Province, Natural Science Foundation of Jiangsu Province, Nanjing University, Nanjing Drum Tower Hospital
Openalex Percentile: Top 54%
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
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