Factors that predict development of chronic kidney disease in patients with rheumatoid arthritis receiving biologic DMARDs and mortality rates

• Published in: International journal of rheumatic diseases 2024-01, Vol.27 (1), p.e14967-n/a
• Main Authors: Sandal Uzun, Güllü, Taghiyeva, Arzu, Çakır, İbrahim Y., Moral, Kenan, Yardımcı, Gözde Kübra, Bölek, Ertuğrul Ç., Farisoğulları, Bayram, Duran, Emine, Ayan, Gizem, Özsoy, Zehra, Ekici, Mustafa, Unaldı, Erdinç, Germe, Şerife A., Fırlatan, Büşra, Kart‐Bayram, Gözde S., Bilgin, Emre, Kılıç, Levent, Karadağ, Ömer, Akdoğan, Ali, Bilgen, Şule A., Kiraz, Sedat, Ertenli, Ali Ihsan, Kalyoncu, Umut
• Format: Article
• Language: English
• Subjects: biological therapy; chronic kidney disease; comorbidities; development; mortality; rheumatoid arthritis
• ISSN: 1756-1841; 1756-185X
• DOI: 10.1111/1756-185X.14967

Objectives We aimed to determine the choice of biologic/targeted synthetic disease‐modifying anti‐rheumatic drugs (b/ts‐DMARDs), factors associated with the development of chronic kidney disease (CKD), and mortality in RA patients with CKD receiving b/ts‐DMARDs. Methods Two thousand one hundred forty‐one RA (79.4% female) patients were included in the analysis from the HUR‐BIO prospective registry. Patients were divided into the CKD group and the non‐CKD group. Age and gender‐matched patients were selected from the non‐CKD group, and then three main groups were determined. CKD was staged according to the glomerular filtration rate criteria. The clinical characteristics of the patients, disease activities, treatment choices, drug retention rate, and mortality rates were compared between the groups. Results CKD was detected in 90/2141 (4.2%) RA patients on b/ts‐DMARDs. Forty patients (2.3%) developed CKD during follow‐up after the initiation of b/ts‐DMARDs. In the CKD group, anti‐TNF agents were chosen as the first‐line b/ts‐DMARDs therapy in 64.4% of patients, with etanercept leading in 31 (34.4%) patients. In multivariate analysis, age at the start of treatment, DAS‐28‐ESR at last visit, amyloidosis, hypertension, and history of smoking were the factors associated with the development of CKD in RA patients receiving b/ts‐DMARDs. The mortality rate in RA‐CKD patients until the onset of the pandemic was 15.41 per 1000 patient years, whereas it was 85.9 per 1000 patient years after the pandemic. Conclusion Comorbidities and control of disease activity are critical in the development of CKD in RA patients receiving b/ts‐DMARDs. While there was no significant difference in mortality rate between CKD and non‐CKD patients, the overall mortality rate increased after the COVID‐19 pandemic duration in both groups.