Department of Biosystems Science and Engineering, ETH Zurich, Basel, Switzerland.
Swiss Institute of Bioinformatics (SIB), Lausanne, Switzerland.
Aliment Pharmacol Ther. 2018 Jan;47(1):55-66. doi: 10.1111/apt.14378. Epub 2017 Oct 20.
Smoking is a strong environmental factor leading to adverse outcomes in Crohn's disease, but a more benign course in ulcerative colitis. Several single nucleotide polymorphisms (SNPs) are associated with smoking quantity and behaviour.
To assess whether smoking-associated SNPs interact with smoking to influence the clinical course of inflammatory bowel diseases.
Genetic and prospectively obtained clinical data from 1434 Swiss inflammatory bowel disease cohort patients (821 Crohn's disease and 613 ulcerative colitis) were analysed. Six SNPs associated with smoking quantity and behaviour (rs588765, rs1051730, rs1329650, rs4105144, rs6474412 and rs3733829) were combined to form a risk score (range: 0-12) by adding the number of risk alleles. We calculated multivariate models for smoking, risk of surgery, fistula, Crohn's disease location and ulcerative colitis disease extent.
In Crohn's disease patients who smoke, the number of surgeries was associated with the genetic risk score. This translates to a predicted 3.5-fold (95% confidence interval: 2.4- to 5.7-fold, P<.0001) higher number of surgical procedures in smokers with 12 risk alleles than individuals with the lowest risk. Patients with a risk score >7 had a significantly shorter time to first intestinal surgery. The genetic risk score did not predict surgery in ulcerative colitis or occurrence of fistulae in Crohn's disease. SNP rs6265 was associated with ileal disease in Crohn's disease (P<.05) and proctitis in ulcerative colitis (P<.05).
SNPs associated with smoking quantity is associated with an increased risk for surgery in Crohn's disease patients who smoke. Our data provide an example of genetics interacting with the environment to influence the disease course of inflammatory bowel disease.
吸烟是导致克罗恩病不良结局的一个重要环境因素,但在溃疡性结肠炎中则呈现出更为良性的病程。一些单核苷酸多态性(SNP)与吸烟量和行为有关。
评估与吸烟相关的 SNP 是否与吸烟相互作用,从而影响炎症性肠病的临床病程。
分析了来自 1434 名瑞士炎症性肠病队列患者(821 名克罗恩病和 613 名溃疡性结肠炎)的遗传和前瞻性临床数据。将与吸烟量和行为相关的 6 个 SNP(rs588765、rs1051730、rs1329650、rs4105144、rs6474412 和 rs3733829)组合成一个风险评分(范围:0-12),通过累加风险等位基因的数量来实现。我们计算了吸烟、手术风险、瘘管、克罗恩病部位和溃疡性结肠炎疾病范围的多变量模型。
在吸烟的克罗恩病患者中,手术次数与遗传风险评分相关。这意味着,在携带 12 个风险等位基因的吸烟者中,手术次数预计会增加 3.5 倍(95%置信区间:2.4-5.7 倍,P<.0001),而在风险最低的个体中则为 1 倍。风险评分>7 的患者首次接受肠道手术的时间显著缩短。遗传风险评分不能预测溃疡性结肠炎的手术或克罗恩病瘘管的发生。SNP rs6265 与克罗恩病的回肠疾病(P<.05)和溃疡性结肠炎的直肠炎(P<.05)相关。
与吸烟量相关的 SNP 与吸烟的克罗恩病患者手术风险增加相关。我们的数据提供了一个遗传与环境相互作用影响炎症性肠病病程的例子。