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An Analysis of Real-World Data on the Safety of Etanercept in Older Patients with Rheumatoid Arthritis
Christopher J Edwards1, Jack F Bukowski2, Sara M Burns3
1Rheumatology Department, NIHR Clinical Research Facility, University Hospital Southampton NHS Foundation Trust, Tremona Road, Southampton, SO16 6YD, UK. cedwards@soton.ac.uk.
Objective:
The aim of this study was to use real-world data to evaluate potential interactions between age, treatment, and the risk of developing four adverse events (AEs) common in the elderly: congestive heart failure, serious infections, non-melanoma skin cancer, and interstitial lung disease. These AEs were identified as important in a prior age-based analysis (≤ 65 vs > 65 years) of etanercept- or placebo-treated patients with rheumatoid arthritis (RA) in controlled clinical trials.
Methods:
Real-world data (1 January 2013 to 31 January 2018) were obtained from the IBM Watson Health MarketScan® Database. Patients were included if aged ≥ 18 years, enrolled for ≥ 1 year prior to RA diagnosis, and without any of the four AEs of interest prior to RA diagnosis or between RA diagnosis and first etanercept exposure. Logistic regression analysis was applied following propensity matching of patients receiving or not receiving etanercept based on age at diagnosis, age status at the beginning of observation (> 65 years or not), sex, geographic region, and follow-up duration.
Results:
The overall cohort comprised 403,689 patients. The absolute risk of each of the four AEs increased with age. In propensity-matched cohorts, etanercept was associated with significantly higher odds of developing each of the four AEs (p < 0.001 for all). However, the relative risk of experiencing the four AEs in patients who received etanercept versus those who did not was similar between patients ≤ 65 years of age and those > 65 years of age.
Conclusions:
In patients with RA, the relative increase in etanercept-associated risk of experiencing congestive heart failure, serious infection, non-melanoma skin cancer, or interstitial lung disease was similar between elderly and non-elderly.
Insights
This study found that while etanercept use increases the risk of four adverse events in rheumatoid arthritis patients, this relative risk is similar for both elderly and non-elderly individuals. The study highlights age-independent safety profiles for etanercept concerning these specific adverse events.
Area of Science:
- Rheumatology
- Pharmacovigilance
- Real-world evidence
Background:
- Rheumatoid arthritis (RA) treatment involves medications like etanercept.
- Elderly patients may have different risks for adverse events (AEs).
- Four key AEs (congestive heart failure, serious infections, non-melanoma skin cancer, interstitial lung disease) were previously identified as important in RA patients.
Purpose of the Study:
- To evaluate the interaction between age, etanercept treatment, and the risk of four specific AEs in RA patients using real-world data.
- To compare the relative risk of these AEs between elderly (>65 years) and non-elderly (≤65 years) RA patients treated with etanercept.
Main Methods:
- Utilized real-world data from the IBM Watson Health MarketScan Database (2013-2018).
- Included RA patients aged ≥18 years with at least 1 year of enrollment prior to diagnosis and no prior AEs.
- Employed propensity score matching and logistic regression to compare etanercept users and non-users, analyzing age as a key factor.
Main Results:
- The overall cohort included 403,689 patients.
- Absolute risk for all four AEs increased with age.
- Etanercept was associated with significantly higher odds of all four AEs (p<0.001).
- Crucially, the relative risk of these AEs with etanercept was similar between patients ≤65 years and >65 years.
Conclusions:
- In RA patients, the relative increase in risk for congestive heart failure, serious infection, non-melanoma skin cancer, or interstitial lung disease associated with etanercept is consistent across elderly and non-elderly populations.
- Age does not appear to modify the relative safety profile of etanercept concerning these specific adverse events.
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