TY - JOUR T1 - Tuberculosis Screening Before and During Treatment with Tumor Necrosis Factor Antagonists: Something Old, Something New JF - The Journal of Rheumatology JO - J Rheumatol SP - 1938 LP - 1940 DO - 10.3899/jrheum.131218 VL - 40 IS - 12 AU - GULEN HATEMI AU - HASAN YAZICI Y1 - 2013/12/01 UR - http://www.jrheum.org/content/40/12/1938.abstract N2 - The increased risk of tuberculosis (TB) with tumor necrosis factor (TNF-α) antagonist treatment is well recognized1. The risk seems to parallel the background risk of TB. In Spain, where the incidence in the general population is 23/100,000, the incidence risk ratio of TB was 4.13 (95% CI 2.59–6.83) in patients with rheumatoid arthritis (RA) compared to the general population and 19.9 (95% CI 16.2–24.8) in patients with RA who were exposed to TNF-α antagonists compared to those who were not. In Sweden, where the incidence is 5/100,000, the incidence risk ratio was 2.0 (95% CI 1.2–3.4) in patients with RA and 4.0 (95% CI 1.3–12) in patients with RA using TNF-α antagonists1,2. In more than half of the patients, TB during TNF-α antagonist use is extrapulmonary and/or disseminated1. There seems to be a bimodal pattern with reactivation of latent TB early during the treatment course, with primary active TB usually developing later in the course. After the implementation of routine screening programs, with increased awareness of the clinical and radiological clues along with use of the tuberculin skin test (TST) and interferon-γ (IFN-γ) release assays (IGRA), a significant decrease in TB reactivation was observed among patients using TNF-α antagonists3. However, there is still no consensus on whether TST or IGRA should be preferred for screening in these patients, who are usually immunocompromised because of the character of their diseases and the immunosuppressives they use. In this issue of The Journal, Costantino, et al4 report the results of TST and T-SPOT.TB assay in a large cohort of patients who are candidates for TNF-α antagonist therapy.The TST is a time-honored method of showing that one has been exposed to mycobacteria. Its potential shortcomings are giving false-positive results because of … Address correspondence to Dr. G. Hatemi, Associate Professor, Istanbul University, Cerrahpasa Medical School, Department of Internal Medicine, Division of Rheumatology, Istanbul 34300, Turkey. E-mail: gulenhatemi{at}yahoo.com ER -