Work

Association of rheumatoid arthritis with chronic kidney disease

Year: 2025

Type: article

Abstract: ABSTRACT Background Rheumatoid arthritis (RA) has been linked to an increased risk of chronic kidney disease (CKD), but the predominant renal phenotype and its independence from established risk factors remain unclear. We examined the RA–CKD association in a large, population-based cohort. Methods RA and CKD were defined using American College of Rheumatology/European Alliance of Associations for Rheumatology and KDIGO criteria. Logistic regression models were employed with stepwise adjustment: first for cardiovascular risk [Systematic COronary Risk Evaluation 2 (SCORE2)], followed by a model including age, sex, metabolic syndrome, smoking status, non-steroidal anti-inflammatory drug (NSAID) use and high-sensitivity C-reactive protein. Interaction terms were tested to evaluate effect modification. Results Among 9665 participants from the Paracelsus 10,000 cohort, 296 (3.1%) had RA. CKD prevalence was higher in the RA group compared with controls (11.8% vs 6.7%, P < .001). Albuminuria at preserved estimated glomerular filtration rate was the dominant renal manifestation in RA (6.8% vs 4.2%, P = .027). In unadjusted analyses, RA was associated with higher odds of CKD [odds ratio (OR) 1.86, 95% confidence interval (CI) 1.30–2.68], an association that persisted after cardiovascular risk adjustment. However, the association was attenuated and no longer statistically significant in the fully adjusted model (OR 1.43, 95% CI 0.96–2.13). A significant interaction was observed with NSAID use (P = .042), whereby the association was largely confined to RA patients not using NSAIDs. Conclusions RA is associated with a higher prevalence of CKD, primarily driven by albuminuria at preserved kidney function. This distinct renal phenotype appears largely mediated by metabolic comorbidities rather than inflammation alone. Our findings highlight the need for systematic albuminuria screening in RA patients to enable earlier detection and intervention.

Source: Clinical Kidney Journal

DOI: 10.1093/ckj/sfaf391