# Impact of Seropositivity on Mortality and Extra-Articular Manifestations in Rheumatoid Arthritis: A Nationwide Propensity-Matched Cohort Study

**Authors:** Ahmad Alomari, Qusai Alqudah, Geran Maule, Aseed Mestarihi, Samah Al-Omari, Osama Obeidat, Reem Elmusa, Abdallah Rayyan, Omar Obeidat, Safwan Alomari, Diala Alawneh

PMC · DOI: 10.31138/mjr.150425.smr · 2025-12-31

## TL;DR

This study compares outcomes in seropositive and seronegative rheumatoid arthritis patients, finding that seropositive RA is linked to higher mortality and more severe complications.

## Contribution

The study provides real-world evidence of the clinical differences between seropositive and seronegative RA using a large, nationwide cohort.

## Key findings

- Seropositive RA patients had higher all-cause mortality compared to seronegative RA patients.
- Seropositive RA was associated with increased risks of joint damage, steroid dependence, and interstitial lung disease.
- Autoantibody status in RA patients is important for predicting disease severity and complications.

## Abstract

Rheumatoid arthritis (RA) is a chronic autoimmune disease that manifests as either seropositive or seronegative subtypes. Seropositive RA is often linked to more severe joint damage and systemic complications. In contrast, seronegative RA has a less defined clinical profile but may still present with significant comorbidities. This study aims to compare clinical outcomes between these RA subtypes using real-world data from the TriNetX Research Network.

A retrospective cohort study analysed adult RA patients from 2015 to 2025, categorised as seropositive or seronegative using International Classification of Diseases, 10th Revision (ICD-10 codes). The primary outcome was all-cause mortality, while secondary outcomes included hospitalization, steroid dependence, disease-modifying antirheumatic drug (DMARD) use, RA-related joint damage, interstitial lung disease (ILD), and coronary artery disease (CAD).

Among 106,492 matched patients (53,246 per cohort), seropositive RA patients had higher all-cause mortality (OR: 1.241; p < 0.001) and increased risks of DMARD use, steroid dependence, and joint damage. They also showed a greater incidence of ILD (OR: 2.419; p < 0.001), CAD indicating a more severe disease course.

This study highlights significant differences in several clinical outcomes between seropositive and seronegative RA patients. These findings highlight the more aggressive nature of seropositive disease and its extra-articular involvement and reinforce the importance of autoantibody status in prognostication and risk stratification for RA patients.

## Linked entities

- **Diseases:** Rheumatoid arthritis (MONDO:0008383), Interstitial lung disease (MONDO:0015925), Coronary artery disease (MONDO:0005010)

## Full-text entities

- **Genes:** PRTN3 (proteinase 3) [NCBI Gene 5657] {aka ACPA, AGP7, C-ANCA, CANCA, MBN, MBT}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, AP2B1 (adaptor related protein complex 2 subunit beta 1) [NCBI Gene 163] {aka ADTB2, AP105B, AP2-BETA, CLAPB1}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, ACE (angiotensin I converting enzyme) [NCBI Gene 1636] {aka ACE1, CD143, DCP, DCP1}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, HLA-DRB1 (major histocompatibility complex, class II, DR beta 1) [NCBI Gene 3123] {aka DRB1, HLA-DR1B, HLA-DRB, SS1}, FGB (fibrinogen beta chain) [NCBI Gene 2244] {aka HEL-S-78p}
- **Diseases:** auto-immune disease (MESH:C538437), lung disease (MESH:D008171), connective tissue disease (MESH:D003240), inflammation (MESH:D007249), Ankylosing spondylitis (MESH:D013167), dislocations (MESH:D004204), steroid dependence (MESH:D009404), CAD (MESH:D003324), PAH (MESH:D000081029), CKD (MESH:D051436), arthritis (MESH:D001168), Overweight (MESH:D050177), Enteropathic arthropathies (MESH:D007592), death (MESH:D003643), CVD (MESH:D002318), Spinal enthesopathy (MESH:D000070676), disease (MESH:D004194), cardiovascular and respiratory diseases (MESH:D012140), atherosclerosis (MESH:D050197), PH (MESH:D006976), bone damage (MESH:D001847), Arthropathic psoriasis (MESH:D011565), SLE (MESH:D008180), synovitis (MESH:D013585), Sacroiliitis (MESH:D058566), -Articular Manifestations (MESH:D012877), steroid (MESH:D016114), seropositive (MESH:D006679), RA (MESH:D001172), Type 2 diabetes mellitus (MESH:D003924), fibrosis (MESH:D005355), ARTIFICIAL (MESH:D060437), Disorders of lipoprotein metabolism (MESH:C563618), joint deformities (MESH:D016916), Nicotine dependence (MESH:D014029), myositis (MESH:D009220), ILD (MESH:D017563), erosions (MESH:D014077), joint destruction (MESH:D008105), hypertension (MESH:D006973), Juvenile arthritis (MESH:D001171), autoimmune disease (MESH:D001327), obesity (MESH:D009765), ACS (MESH:D054058), rheumatoid vasculitis (MESH:D056653), stroke (MESH:D020521), UIP (MESH:D054990), lipidemias (MESH:D006949)
- **Chemicals:** Spironolactone (MESH:D013148), Blood glucose (MESH:D001786), Thiazides (MESH:D049971), Insulin (MESH:D007328), Prasugrel (MESH:D000068799), steroid (MESH:D013256), Clopidogrel (MESH:D000077144), Aspirin (MESH:D001241), Cangrelor (MESH:C117446), Ticagrelor (MESH:D000077486), Angiotensin II inhibitors (-), insulins (MESH:D061385), lipid (MESH:D008055)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12835916/full.md

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Source: https://tomesphere.com/paper/PMC12835916