Sonntag Barbara, Stolze Birgit, Heinecke Achim, Luegering Andreas, Heidemann Jan, Lebiedz Pia, Rijcken Emile, Kiesel Ludwig, Domschke Wolfram, Kucharzik Torsten, Maaser Christian
Department of Obstetrics and Gynecology, University of Muenster, Muenster, Germany.
Inflamm Bowel Dis. 2007 Nov;13(11):1385-90. doi: 10.1002/ibd.20206.
Exposure to bacterial antigens and other environmental factors in combination with a genetic susceptibility have been implicated in the etiology of inflammatory bowel disease (IBD). As certain perinatal circumstances, e.g., delivery by cesarean section, predispose to a different intestinal colonizations the aim of this analysis was to define a potential influence on the development of IBD in later life.
In a case-control study design, birth data were recorded from patients diagnosed with IBD (Crohn's disease [CD], n = 1,096; ulcerative colitis [UC], n = 763) and healthy controls ([C], n = 878) by a self-administered questionnaire.
Preterm birth (CD: odds ratio [OR] 1.5 [95% confidence interval 1.1-2.0], UC: OR 1.3 [0.9-1.9]), mother's disease during pregnancy (CD: OR 1.9 [1.3-2.9], UC: OR 1.6 [1.0-2.4]), and disease in the first year of life (CD: OR 2.2 [1.6-2.9], UC: OR 1.7 [1.3-2.3]) are associated with the development of IBD in later life. No significant associations were found for the mode of delivery and breast feeding. In a logistic regression analysis female sex, smoking, appendectomy, maternal IBD, and disease in the first year of life were independently associated with CD. Female sex, appendectomy, and disease in the first year of life were independently associated with UC.
Preterm birth and other perinatal circumstances are associated with the development of IBD, of which disease in the first year of life is an independent risk factor in multivariate analysis.
接触细菌抗原和其他环境因素,再加上遗传易感性,被认为与炎症性肠病(IBD)的病因有关。由于某些围产期情况,例如剖宫产分娩,会导致不同的肠道菌群定植,因此本分析的目的是确定其对晚年IBD发病的潜在影响。
在一项病例对照研究设计中,通过自行填写的问卷记录了诊断为IBD(克罗恩病[CD],n = 1096;溃疡性结肠炎[UC],n = 763)的患者和健康对照者([C],n = 878)的出生数据。
早产(CD:比值比[OR] 1.5 [95%置信区间1.1 - 2.0],UC:OR 1.3 [0.9 - 1.9])、母亲孕期患病(CD:OR 1.9 [1.3 - 2.9],UC:OR 1.6 [1.0 - 2.4])以及生命第一年患病(CD:OR 2.2 [1.6 - 2.9],UC:OR 1.7 [1.3 - 2.3])与晚年IBD的发病相关。未发现分娩方式和母乳喂养有显著关联。在逻辑回归分析中,女性、吸烟、阑尾切除术、母亲患IBD以及生命第一年患病与CD独立相关。女性、阑尾切除术以及生命第一年患病与UC独立相关。
早产和其他围产期情况与IBD的发病相关,其中生命第一年患病在多变量分析中是一个独立的危险因素。