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Cumulative incidence and risk of infection in patients with rheumatoid arthritis treated with janus kinase inhibitors: A systematic review and meta-analysis.
- Source :
-
PloS one [PLoS One] 2024 Jul 31; Vol. 19 (7), pp. e0306548. Date of Electronic Publication: 2024 Jul 31 (Print Publication: 2024). - Publication Year :
- 2024
-
Abstract
- Patients with rheumatoid arthritis (RA) who receive immunosuppressive medications have a heightened risk of infection. The goal of our study was to calculate the pooled cumulative incidence and risk of infection in patients with RA treated with Janus kinase inhibitors (JAKi). The PubMed and EMBASE databases were queried for randomized controlled trials comparing patients with RA treated with JAKi (upadacitinib, baricitinib, tofacitinib, peficitinib, or filgotinib), defined as the treatment group, compared with control subjects, defined as participants receiving placebo or treatment regimen that was similar to that of participants in the treatment group, with the exception of JAKi. The primary study endpoint was the relative risk (RR) of any-grade and severe infection. The secondary endpoints were RR and cumulative incidence of opportunistic infections, herpes zoster, and pneumonia. The Stata v17 software was used for all data analysis. Results showed that treatment with baricitinib was associated with an increased risk of any-grade (RR 1.34; 95% CI: 1.19-1.52) and opportunistic (RR 2.69; 95% CI: 1.22-5.94) infection, whereas treatment with filgotinib (RR 1.21; 95% CI: 1.05-1.39), peficitinib (RR 1.40; 95% CI: 1.05-1.86) and upadacitinib (RR 1.30; 95% CI: 1.09-1.56) was associated with increased risk of any-grade infection only. Analysis based on type of infection showed a pooled cumulative incidence of 32.44% for any-grade infections, 2.02% for severe infections, 1.74% for opportunistic infections, 1.56% for herpes zoster, and 0.49% for pneumonia in patients treated with any JAKi during the follow-up period. Treatment with specific JAKi in patients with RA is associated with an increased risk of any-grade and opportunistic infections but not severe infection. Close clinical monitoring of patients with RA treated with JAKi is required to establish the long-term infection risk profile of these agents.<br />Competing Interests: The authors have declared that no competing interests exist.<br /> (Copyright: © 2024 Ouranos et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.)
- Subjects :
- Humans
Incidence
Herpes Zoster epidemiology
Herpes Zoster chemically induced
Opportunistic Infections epidemiology
Opportunistic Infections chemically induced
Pyrroles adverse effects
Pyrroles therapeutic use
Niacinamide analogs & derivatives
Niacinamide adverse effects
Niacinamide therapeutic use
Infections epidemiology
Infections chemically induced
Randomized Controlled Trials as Topic
Heterocyclic Compounds, 3-Ring adverse effects
Heterocyclic Compounds, 3-Ring therapeutic use
Antirheumatic Agents adverse effects
Antirheumatic Agents therapeutic use
Triazoles adverse effects
Triazoles therapeutic use
Adamantane analogs & derivatives
Pyridines
Arthritis, Rheumatoid drug therapy
Arthritis, Rheumatoid complications
Janus Kinase Inhibitors adverse effects
Janus Kinase Inhibitors therapeutic use
Azetidines adverse effects
Azetidines therapeutic use
Purines adverse effects
Purines therapeutic use
Pyrazoles adverse effects
Pyrazoles therapeutic use
Pyrimidines adverse effects
Pyrimidines therapeutic use
Piperidines adverse effects
Piperidines therapeutic use
Sulfonamides adverse effects
Sulfonamides therapeutic use
Subjects
Details
- Language :
- English
- ISSN :
- 1932-6203
- Volume :
- 19
- Issue :
- 7
- Database :
- MEDLINE
- Journal :
- PloS one
- Publication Type :
- Academic Journal
- Accession number :
- 39083492
- Full Text :
- https://doi.org/10.1371/journal.pone.0306548