PMID- 31674159 OWN - NLM STAT- MEDLINE DCOM- 20200407 LR - 20200408 IS - 1598-6357 (Electronic) IS - 1011-8934 (Print) IS - 1011-8934 (Linking) VI - 34 IP - 42 DP - 2019 Nov 4 TI - The Effect of Tumor Necrosis Factor-Alpha Inhibitors on Uveitis in Patients with Ankylosing Spondylitis. PG - e278 LID - 10.3346/jkms.2019.34.e278 [doi] LID - e278 AB - BACKGROUND: Tumor necrosis factor-alpha (TNF-alpha) inhibitors (TNFis), which are the main treatment for ankylosing spondylitis (AS), have been reported not only to reduce the incidence of anterior uveitis (AU) but also to induce it, and these effects differ among the various types of TNFis in clinical use. The present study investigated the effect of TNFis on uveitis by analyzing the long-term clinical course of AU in AS patients treated with TNFi therapy. METHODS: Patients treated with at least one TNFi between January 2007 and July 2017 were reviewed, and 54 patients with at least one episode of AU were included in this study. The TNFis included anti-TNF-alpha antibodies (adalimumab, infliximab, and golimumab), and a soluble TNF receptor molecule (etanercept). The effect of prevention of AU, the likelihood of new-onset uveitis after the initiation of TNFi therapy, and the effects of drug switching and dose escalation were assessed. RESULTS: The first uveitis flare was observed before TNFi therapy in 39 patients and after TNFi therapy in 15 patients. Anti-TNF-alpha antibodies were more efficacious in decreasing the recurrence of AU than etanercept. Among patients in which uveitis first occurred after beginning TNFi therapy, patients on etanercept tended to first develop AU less than 1 year after starting the drug, and their AS tended to be well-controlled at the time of uveitis flares. Patients with a uveitis flare before their medication was switched did not recur afterwards, and five of eight patients showed no relapse after dose escalation. CONCLUSION: TNFis have various effects on AU. TNFis, particularly anti-TNF-alpha antibodies, should be considered in patients with AS and frequent AU relapse. Additionally, clinicians should consider whether AU is due to an absence of a therapeutic response of AS to TNFi treatment or to TNFi treatment itself, and appropriate treatment changes should be made accordingly. CI - (c) 2019 The Korean Academy of Medical Sciences. FAU - Lee, Suhwan AU - Lee S AUID- ORCID: 0000-0002-7065-8735 AD - Department of Ophthalmology, Kangwon National University Hospital, Kangwon National University Graduate School of Medicine, Chuncheon, Korea. FAU - Park, Yu Jeong AU - Park YJ AUID- ORCID: 0000-0002-0609-8614 AD - Department of Ophthalmology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea. FAU - Lee, Joo Yong AU - Lee JY AUID- ORCID: 0000-0002-2187-196X AD - Department of Ophthalmology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea. ophthalmo@amc.seoul.kr. LA - eng GR - NRF2018R1D1A1A02045583/NRF/National Research Foundation of Korea/Korea GR - 16-484/Asan Institute for Life Sciences, Asan Medical Center/Korea PT - Journal Article DEP - 20191104 PL - Korea (South) TA - J Korean Med Sci JT - Journal of Korean medical science JID - 8703518 RN - 0 (Antibodies, Monoclonal) RN - 0 (TNF protein, human) RN - 0 (Tumor Necrosis Factor-alpha) RN - 91X1KLU43E (golimumab) RN - B72HH48FLU (Infliximab) RN - FYS6T7F842 (Adalimumab) RN - OP401G7OJC (Etanercept) SB - IM MH - Adalimumab/therapeutic use MH - Adult MH - Aged MH - Antibodies, Monoclonal/therapeutic use MH - Etanercept/therapeutic use MH - Female MH - Humans MH - Infliximab/therapeutic use MH - Kaplan-Meier Estimate MH - Male MH - Middle Aged MH - Recurrence MH - Retrospective Studies MH - Spondylitis, Ankylosing/complications/*drug therapy MH - Tumor Necrosis Factor-alpha/*antagonists & inhibitors MH - Uveitis/complications/*drug therapy MH - Young Adult PMC - PMC6823519 OTO - NOTNLM OT - Adalimumab OT - Ankylosing Spondylitis OT - Anterior Uveitis OT - Etanercept OT - Infliximab OT - Tumor Necrosis Factor-Alpha COIS- The authors have no potential conflicts of interest to disclose. EDAT- 2019/11/02 06:00 MHDA- 2020/04/09 06:00 PMCR- 2019/11/04 CRDT- 2019/11/02 06:00 PHST- 2019/05/29 00:00 [received] PHST- 2019/09/23 00:00 [accepted] PHST- 2019/11/02 06:00 [entrez] PHST- 2019/11/02 06:00 [pubmed] PHST- 2020/04/09 06:00 [medline] PHST- 2019/11/04 00:00 [pmc-release] AID - 34.e278 [pii] AID - 10.3346/jkms.2019.34.e278 [doi] PST - epublish SO - J Korean Med Sci. 2019 Nov 4;34(42):e278. doi: 10.3346/jkms.2019.34.e278.