Cargando…

Safety of tumor necrosis factor-alpha inhibitors for treatment of ankylosing spondylitis: A meta-analysis

BACKGROUND: Ankylosing spondylitis (AS) is a chronic immune-mediated disease affecting the sacroiliac joints and the spine, manifesting with new bone formation and osteopenia. Five tumor necrosis factor-alpha (TNF-α) inhibitors (infliximab, etanercept, adalimumab, certolizumab, and golimumab) are av...

Descripción completa

Detalles Bibliográficos
Autores principales: Ma, Zeren, Liu, Xiaoping, Xu, Xiaosheng, Jiang, Jie, Zhou, Jian, Wang, Jia, Chen, Dewang, Luo, Song
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5484196/
https://www.ncbi.nlm.nih.gov/pubmed/28640088
http://dx.doi.org/10.1097/MD.0000000000007145
Descripción
Sumario:BACKGROUND: Ankylosing spondylitis (AS) is a chronic immune-mediated disease affecting the sacroiliac joints and the spine, manifesting with new bone formation and osteopenia. Five tumor necrosis factor-alpha (TNF-α) inhibitors (infliximab, etanercept, adalimumab, certolizumab, and golimumab) are available for the treatment of AS, however, the results for the safety of TNF-α inhibitors in the treatment of AS are not consistent. METHODS: In this study, we conducted a meta-analysis to determine the safety of TNF-α inhibitors compared with placebo in reducing pain, swelling, and inflammation of AS patients. Eight relevant articles including 2049 patients were included for this meta-analysis study. We observed that the incidence of adverse events (RR  =  1.22, 95% CI: 1.12–1.33; P  =  .501, I(2)  =  0%) and injection-site reaction (RR  =  2.93, 95% CI: 2.02–4.23; P  =  .691, I(2)  =  0%) in AS patients’ treatment with TNF-α inhibitors was significantly higher than that with placebo. RESULTS: However, there was no significant difference in the incidence of serious adverse event, infection, serious infection, and discontinuations due to adverse event. TNF-α inhibitors may be a promising treatment for AS, but carries an increased incidence rate of adverse events and injection-site reaction. CONCLUSION: Due to the existence of the unstable factors, further studies need to be done to verify the result of this study.