Department of Pediatrics, Hsinchu MacKay Memorial Hospital, Hsinchu city 300, Taiwan.
Division of Rheumatology, Department of Internal Medicine, Taoyuan General Hospital, Ministry of Health and Welfare, Taoyuan 330, Taiwan.
Int J Environ Res Public Health. 2018 Nov 21;15(11):2602. doi: 10.3390/ijerph15112602.
Both periodontal disease (PD) and inflammatory bowel disease (IBD), including Crohn's disease (CD) and ulcerative colitis (UC), are important diseases of the alimentary tract. Microbiome and immune-mediated inflammatory processes play important roles in these diseases. An association between PD and IBD may exist. This study investigated the risk of IBD in patients with PD. This study used data from the National Health Insurance Research Database of Taiwan from 1996 to 2013. A total of 27,041 patients with PD were enrolled as a study group, and 108,149 patients without PD were selected as the control group after matching by gender, age, insured region, urbanization, and income with a 1:4 ratio. Cox proportional hazards regression was used to calculate the risk of IBD. Of the 135,190 participants enrolled in this study, 5392 (4%) with newly diagnosed IBD were identified. The overall incidence of subsequent IBD was similar in both groups (3.8% vs. 4%, adjusted hazard ratio (aHR) = 1.01, 95% confidence interval (CI): 0.94⁻1.08). However, an increased risk of UC in the PD group was found after adjusting confounding factors (aHR: 1.56, 95% CI: 1.13⁻2.15; < 0.05). This study demonstrated that patients with PD had approximately one-half higher risk of subsequent UC. Further studies are warranted to elucidate the relationship between PD and UC.
牙周病(PD)和炎症性肠病(IBD),包括克罗恩病(CD)和溃疡性结肠炎(UC),都是重要的消化道疾病。微生物组和免疫介导的炎症过程在这些疾病中发挥着重要作用。PD 和 IBD 之间可能存在关联。本研究调查了 PD 患者发生 IBD 的风险。本研究使用了来自台湾 1996 年至 2013 年的全民健康保险研究数据库的数据。共纳入 27041 例 PD 患者作为研究组,按照性别、年龄、参保地区、城市化程度和收入,以 1:4 的比例匹配了 108149 例无 PD 患者作为对照组。采用 Cox 比例风险回归计算 IBD 的发病风险。在这项研究中,共纳入了 135190 名参与者,其中有 5392 名(4%)患者被诊断为新发 IBD。两组患者的后续 IBD 总体发病率相似(3.8%比 4%,调整后的危险比[aHR]为 1.01,95%置信区间[CI]:0.94⁻1.08)。然而,在调整混杂因素后,PD 组发生 UC 的风险增加(aHR:1.56,95% CI:1.13⁻2.15;<0.05)。本研究表明,PD 患者发生后续 UC 的风险大约增加了一半。需要进一步的研究来阐明 PD 和 UC 之间的关系。