Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
Statistics and Data Center, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
Aliment Pharmacol Ther. 2019 Jan;49(2):165-172. doi: 10.1111/apt.15076. Epub 2018 Dec 2.
Although a higher risk of other immune-mediated diseases has been reported in inflammatory bowel disease (IBD) patients, the risk factors of immune-mediated diseases development and the effect of concomitant immune-mediated diseases on outcomes remain poorly defined.
To determine the risk factors of incident immune-mediated diseases and the impact of comorbid immune-mediated diseases on outcomes in IBD.
Using the National Health Insurance claims data for the entire Korean population, we identified 35 581 IBD patients without immune-mediated diseases and 595 IBD patients with immune-mediated diseases from 2012 to 2013, and follow-up until 2016. We selected four controls by age and sex for comparing with cases.
A total of 35 581 IBD patients without immune-mediated diseases and 142 324 matched controls without immune-mediated diseases were followed from 2014 to 2016 and of these 239 IBD patients and 357 controls developed immune-mediated disease. The overall immune-mediated diseases risk was higher in IBD patients (HR, hazard ratio, 2.47; 95% confidence interval, CI, 2.09-2.91). In a nested case-control study of the IBD cohort, adult patients aged ≥20 years and frequent hospitalisation ≥1 per year were independent risk factors for incident immune-mediated diseases, in contrast, 5-aminosalicylic acid (5-ASA) use had protective effect (odds ratio, 0.61; 95% CI, 0.41-0.90) for developing immune-mediated diseases. In addition, IBD patients with another immune-mediated disease had an increased risk of needing anti-TNF-α agent (HR, 2.40; 95% CI, 2.02-2.84) and developing acute flare (HR, 1.76; 95% CI, 1.37-2.26).
The incidence of immune-mediated diseases in IBD patients was higher than that of non-IBD population. 5-ASA use may reduce this risk.
虽然炎症性肠病(IBD)患者发生其他免疫介导性疾病的风险较高,但免疫介导性疾病发生的危险因素以及并存的免疫介导性疾病对结局的影响仍不清楚。
确定 IBD 患者发生免疫介导性疾病的危险因素及并存免疫介导性疾病对结局的影响。
利用韩国全民健康保险索赔数据,我们于 2012 年至 2013 年期间从数据库中确定了 35581 例无免疫介导性疾病的 IBD 患者和 595 例有免疫介导性疾病的 IBD 患者,随访至 2016 年。我们按年龄和性别为病例选择了 4 名对照。
在 2014 年至 2016 年随访期间,35581 例无免疫介导性疾病的 IBD 患者中有 239 例和 142324 例无免疫介导性疾病的匹配对照者发生了免疫介导性疾病,357 例对照者发生了免疫介导性疾病。IBD 患者的总体免疫介导性疾病风险较高(HR,风险比,2.47;95%CI,2.09-2.91)。在 IBD 队列的巢式病例对照研究中,≥20 岁的成年患者和每年≥1 次住院的患者是发生免疫介导性疾病的独立危险因素,而 5-氨基水杨酸(5-ASA)的使用对发生免疫介导性疾病具有保护作用(OR,0.61;95%CI,0.41-0.90)。此外,患有另一种免疫介导性疾病的 IBD 患者需要使用抗 TNF-α 药物的风险增加(HR,2.40;95%CI,2.02-2.84),且发生急性发作的风险增加(HR,1.76;95%CI,1.37-2.26)。
IBD 患者免疫介导性疾病的发生率高于非 IBD 人群。5-ASA 的使用可能会降低这种风险。