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Higher risk of tuberculosis in combination therapy for inflammatory bowel disease: A nationwide population-based cohort study in South Korea

机译:炎症性肠病联合治疗的结核病风险较高:韩国全国群体队列研究

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Inflammatory bowel disease (IBD) in Asia has become increasingly prevalent. As a treatment of IBD, many immunomodulators and biological agents were introduced and shown to be effective in inducing and maintaining remission. However, many cases with treatment failure were reported. To overcome the failure, combination therapy of immunomodulatory and biologics have emerged, showing better outcomes by optimizing biologic pharmacokinetics and minimizing immunogenicity. Adversely, rates of tuberculosis (TB) have been increased as a result. The aim of this study is to compare the risk of TB according to the therapy using large population data. We used data from the South Korean Health Insurance and Review Agency over the period 2008–2016 and calculated the hazard ratio (HR) for TB in IBD. We compared the risk of TB according to the medication: infliximab only, azathioprine only (AZA), combination of azathioprine and infliximab (CAI), azathioprine monotherapy and infliximab monotherapy (AIM), and azathioprine and infliximab whether simultaneously or separately (AISS). In IBD patients, a total of 249 patients were identified as active TB. After one-to-one matching with age, sex and disease duration, the risks of TB were significantly higher in AZA group (HR, 2.06; 95% CI, 1.35–3.12, P .001), AIM group (HR, 3.26; 95% CI, 1.18–9.05, P = .02), AISS group (HR, 3.50; 95% CI, 1.92–6.37, P .001), and CAI group (HR, 5.67; 95% CI, 2.42–10.21, P .001), and the HR increased gradually in this order. In UC patients, the results were in similar pattern, but this pattern was not observed in CD patients in our study. Our study shows that Korean IBD patients are at risk of TB, and the risk increases with usage of IBD medication; moreover, the risk is the highest if combination therapy is used. These results highlight the importance of screening for TB in IBD patients, especially in combination therapy.
机译:亚洲炎症性肠病(IBD)越来越普遍。作为IBD的治疗,引入了许多免疫调节剂和生物制剂,并显示有效诱导和维持缓解。然而,报告了许多治疗失败的病例。为了克服失败,出现了免疫调节和生物学的联合治疗,通过优化生物药代动力学和最小化免疫原性,显示出更好的结果。不对不利的是,由于结核病(TB)的速率因此增加了。本研究的目的是根据使用大人口数据的治疗来比较TB的风险。我们在2008 - 2016年期间使用了来自韩国健康保险和审查机构的数据,并计算了IBD中TB的危险比(HR)。我们将根据药物的危险进行比较:仅限英夫利昔单抗(AZA),偶氮嘌呤和英夫利昔单抗(CAI)的组合,偶氮嘌呤单疗法和英美疗法单药治疗(AIM),以及AzathioPrine和Flowiximab是否同时或分开(AISS)。在IBD患者中,共249名患者被鉴定为活性TB。一对一与年龄,性别和疾病持续时间匹配后,AZA组TB的风险显着高(HR,2.06; 95%CI,1.35-3.12,P <.001),AIM组(HR,3.26 ; 95%CI,1.18-9.05,P = .02),AISS组(HR,3.50; 95%CI,1.92-6.37,P <.001)和CAI组(HR,5.67; 95%CI,2.42- 10.21,P <.001),HR按此顺序逐渐增加。在UC患者中,结果具有类似的模式,但在我们的研究中未观察到这种模式。我们的研究表明,韩国IBD患者面临TB的风险,风险随着IBD药物的使用而增加;此外,如果使用联合治疗,则风险是最高的。这些结果突出了IBD患者中TB筛选的重要性,特别是在联合治疗中。

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