Department of Internal Medicine, Kaohsiung Municipal Ta-Tung Hospital, Kaohsiung Medical University Hospital, College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan.
Division of Gastroenterology and Department of Internal Medicine, Kaohsiung Municipal Ta-Tung Hospital, Kaohsiung, Taiwan.
Clin Gastroenterol Hepatol. 2019 Sep;17(10):1991-1999. doi: 10.1016/j.cgh.2018.12.014. Epub 2018 Dec 20.
BACKGROUND & AIMS: Helicobacter pylori induces immune tolerance and is associated with a lower risk for immune-mediated disorders, such as autoimmune and inflammatory bowel diseases (IBD). We aimed to determine the effects of treatment for H pylori infection on the incidence of autoimmune disease and IBD.
We collected data from the National Health Insurance Research Database in Taiwan on patients younger than 18 years old without a prior diagnosis of autoimmune disease or IBD. Patients with peptic ulcer disease (PUD) with treatment of H pylori infection (PUD+HPRx), PUD without H pylori treatment (PUD-HPRx), a urinary tract infection (UTI) treated with cephalosporin, or without PUD (controls) were matched for age, sex, insurance, and Charlson's comorbidity index score.
Of the 1 million patients we collected data from in 2005, we included 79,181 patients in the study. We compared the effects of treatment for H pylori infection on the risk of autoimmunity or IBD and found that PUD+HPRx has the highest adjusted hazard risk (aHR) for autoimmunity or IBD (aHR, 2.36), compared to PUD-HPRx (aHR, 1.91) or UTI (aHRs, 1.71) (P < .001). The increased risk of autoimmune disease was not completely accounted for by antibiotic therapy alone, because PUD+HPRx had a higher aHR than UTI (P < .001). A small but significant increase in mortality was observed in the PUD+HPRx cohort (aHR, 1.11; P = .001).
In an analysis of data from the National Health Insurance Research Database in Taiwan, we found that treatment for H pylori infection is associated with a significant increase in the risk for autoimmune disease, including IBD.
幽门螺杆菌可诱导免疫耐受,与免疫介导的疾病(如自身免疫性和炎症性肠病)的风险降低相关。我们旨在确定幽门螺杆菌感染治疗对自身免疫性疾病和炎症性肠病发病率的影响。
我们从台湾全民健康保险研究数据库中收集了年龄在 18 岁以下且无先前自身免疫性疾病或炎症性肠病诊断的患者的数据。患有幽门螺杆菌感染治疗消化性溃疡病(PUD+HPRx)、未治疗幽门螺杆菌的消化性溃疡病(PUD-HPRx)、头孢菌素治疗的尿路感染(UTI)或无 PUD(对照组)的患者,按年龄、性别、保险和 Charlson 合并症指数评分进行匹配。
在 2005 年收集的 100 万名患者中,我们纳入了 79181 名患者进行研究。我们比较了幽门螺杆菌感染治疗对自身免疫或炎症性肠病风险的影响,发现与 PUD-HPRx(aHR,1.91)或 UTI(aHRs,1.71)相比,PUD+HPRx 治疗幽门螺杆菌感染具有最高的自身免疫或炎症性肠病的调整后风险比(aHR)(aHR,2.36)(P <.001)。抗生素治疗本身并不能完全解释自身免疫性疾病风险的增加,因为 PUD+HPRx 的 aHR 高于 UTI(P <.001)。在 PUD+HPRx 队列中观察到死亡率略有但显著增加(aHR,1.11;P =.001)。
在对台湾全民健康保险研究数据库数据的分析中,我们发现幽门螺杆菌感染治疗与自身免疫性疾病(包括炎症性肠病)风险的显著增加相关。