Gradel Kim O, Nielsen Hans L, Schønheyder Henrik C, Ejlertsen Tove, Kristensen Brian, Nielsen Henrik
Department of Infectious Diseases, Aalborg Hospital, Aarhus University Hospital, Aalborg, Denmark.
Gastroenterology. 2009 Aug;137(2):495-501. doi: 10.1053/j.gastro.2009.04.001. Epub 2009 Apr 8.
BACKGROUND & AIMS: Various commensal enteric and potentially pathogenic bacteria may be involved in the pathogenesis of inflammatory bowel diseases (IBD). We compared the risk of IBD between a cohort of patients with documented Salmonella or Campylobacter gastroenteritis and an age- and gender-matched control group from the same population in Denmark.
We identified 13,324 patients with Salmonella/Campylobacter gastroenteritis from laboratory registries in North Jutland and Aarhus counties, Denmark, from 1991 through 2003, and 26,648 unexposed controls from the same counties. Of these, 176 exposed patients with IBD before the infection, their 352 unexposed controls, and 80 unexposed individuals with IBD before the Salmonella/Campylobacter infection were excluded. The final study cohort of 13,148 exposed and 26,216 unexposed individuals were followed for up to 15 years (mean, 7.5 years).
A first-time diagnosis of IBD was reported in 107 exposed (1.2%) and 73 unexposed individuals (0.5%). By age, gender, and comorbidity adjusted Cox proportional hazards regression analysis, the hazard ratio (95% confidence interval) for IBD was 2.9 (2.2-3.9) for the whole period and 1.9 (1.4-2.6) if the first year after the Salmonella/Campylobacter infection was excluded. The increased risk in exposed subjects was observed throughout the 15-year observation period. The increased risk was similar for Salmonella (n = 6463) and Campylobacter (n = 6685) and for a first-time diagnosis of Crohn's disease (n = 47) and ulcerative colitis (n = 133).
In our population-based cohort study with complete follow-up, an increased risk of IBD was demonstrated in individuals notified in laboratory registries with an episode of Salmonella/Campylobacter gastroenteritis.
多种共生肠道细菌及潜在致病菌可能参与炎症性肠病(IBD)的发病机制。我们比较了丹麦同一人群中一组确诊为沙门氏菌或弯曲杆菌性肠胃炎的患者与年龄和性别匹配的对照组患IBD的风险。
我们从丹麦北日德兰郡和奥胡斯郡的实验室登记处识别出1991年至2003年期间13324例沙门氏菌/弯曲杆菌性肠胃炎患者,以及来自同一郡的26648例未暴露对照组。其中,排除了176例感染前患有IBD的暴露患者、其352例未暴露对照,以及80例沙门氏菌/弯曲杆菌感染前患有IBD的未暴露个体。对最终的研究队列,即13148例暴露个体和26216例未暴露个体进行了长达15年(平均7.5年)的随访。
107例暴露个体(1.2%)和73例未暴露个体(0.5%)首次被诊断为IBD。经年龄、性别和合并症调整的Cox比例风险回归分析,整个期间IBD的风险比(95%置信区间)为2.9(2.2 - 3.9),如果排除沙门氏菌/弯曲杆菌感染后的第一年,则为1.9(1.4 - 2.6)。在整个15年观察期内均观察到暴露个体风险增加。沙门氏菌(n = 6463)和弯曲杆菌(n = 6685)以及克罗恩病(n = 47)和溃疡性结肠炎(n = 133)首次诊断的风险增加情况相似。
在我们进行的具有完整随访的基于人群的队列研究中,实验室登记处记录有沙门氏菌/弯曲杆菌性肠胃炎发作的个体患IBD的风险增加。