Abstract

ObjectiveTo investigate the risk of tuberculosis (TB) among rheumatoid arthritis (RA) patients within 1 year after initiation of tumor necrosis factor inhibitor (TNFi) therapy from 2008 to 2012.MethodsWe used the 2003–2013 Taiwanese National Health Insurance Research Database to identify RA patients who started any RA-related medical therapy from 2008 to 2012. Those who initiated etanercept or adalimumab therapy during 2008–2012 were selected as the TNFi group and those who never received biologic disease-modifying anti-rheumatic drug therapy were identified as the comparison group after excluding the patients who had a history of TB or human immunodeficiency virus infection/acquired immune deficiency syndrome. We used propensity score matching (1:6) for age, sex, and the year of the drug index date to re-select the TNFi group and the non-TNFi controls. After adjusting for potential confounders, hazard ratios (HRs) with 95% confidence intervals (CIs) were calculated to examine the 1-year TB risk in the TNFi group compared with the non-TNFi controls. Subgroup analyses according to the year of treatment initiation and specific TNFi therapy were conducted to assess the trend of 1-year TB risk in TNFi users from 2008 to 2012.ResultsThis study identified 5,349 TNFi-treated RA patients and 32,064 matched non-TNFi-treated controls. The 1-year incidence rates of TB were 1,513 per 105 years among the TNFi group and 235 per 105 years among the non-TNFi controls (incidence rate ratio, 6.44; 95% CI, 4.69–8.33). After adjusting for age, gender, disease duration, comoridities, history of TB, and concomitant medications, TNFi users had an increased 1-year TB risk (HR, 7.19; 95% CI, 4.18–12.34) compared with the non-TNFi-treated controls. The 1-year TB risk in TNFi users increased from 2008 to 2011 and deceased in 2012 when the Food and Drug Administration in Taiwan announced the Risk Management Plan for patients scheduled to receive TNFi therapy.ConclusionThis study showed that the 1-year TB risk in RA patients starting TNFi therapy was significantly higher than that in non-TNFi controls in Taiwan from 2008 to 2012.

Highlights

  • Tuberculosis (TB) is an ancient, contagious airborne disease that has been in existence for centuries; currently, the disease is still an alarming global health issue

  • Subgroup analyses according to the year of treatment initiation and specific Tumor necrosis factor (TNF) inhibitor (TNFi) therapy were conducted to assess the trend of 1-year TB risk in TNFi users from 2008 to 2012

  • This study identified 5,349 TNFi-treated Rheumatoid arthritis (RA) patients and 32,064 matched non-TNFi-treated controls

Read more

Summary

Introduction

Tuberculosis (TB) is an ancient, contagious airborne disease that has been in existence for centuries; currently, the disease is still an alarming global health issue. In 2014, the World Health Organization (WHO) reported 9.6 million incident cases of TB. TB mortality remains one of the leading causes of death worldwide, with the estimated mortality of 1.5 million per year [1]. The Taiwan Centers for Disease Control reported 11,528 cases of TB (49.4 cases per 100,000 populations) and 609 TB-related deaths in 2013[2]. In Taiwan, the risk of TB development was 2.28-fold higher in RA patients than in the general population [8]. The use of a TNF inhibitor (TNFi) in RA patients further increased the TB risk [7, 10,11,12]. Prior studies have shown that monoclonal antibodies to TNF, such as infliximab (IFX) and adalimumab (ADA), may drive higher TB risk than TNF receptor blockers such as etanercept (ETN) [10, 13]

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call