Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota, USA.
Clin Gastroenterol Hepatol. 2013 Sep;11(9):1108-1114.e5. doi: 10.1016/j.cgh.2013.03.024. Epub 2013 Apr 13.
BACKGROUND & AIMS: Central obesity could increase the risk for Barrett's esophagus (BE) and esophageal adenocarcinoma by mechanical and/or metabolic mechanisms, such as hyperinsulinemia. We performed an epidemiologic study to determine whether prior type 2 diabetes mellitus (DM2) is associated with BE.
We performed a population-based case-control study using the General Practice Research Database, a UK primary care database that contains information on more than 8 million subjects, to identify cases of BE (using previously validated codes; n = 14,245) and matched controls without BE (by age, sex, enrollment date, duration of follow-up evaluation, and practice region by incidence density sampling; n = 70,361). We assessed the association of a prior diagnosis of DM2 with BE using conditional univariate and multivariable regression analysis. Confounders assessed included smoking, obesity measured by body mass index (BMI), and gastroesophageal reflux disease.
BE cases were more likely than controls to have smoked (52.4% vs 49.9%), have a higher mean BMI (27.2 vs 26.9), and a higher prevalence of DM2 than controls (5.8% vs 5.3%). On multivariable analysis, DM2 was associated with a 49% increase in the risk of BE, independent of other known risk factors (odds ratio, 1.49; 95% confidence interval, 1.16-1.91). This association was stronger in women than men. Results remained stable with sensitivity analyses.
In a large population-based case-control study, DM2 was a risk factor for BE, independent of obesity (as measured by BMI) and other risk factors (smoking and gastroesophageal reflux disease). These data suggest that metabolic pathways related to DM2 should be explored in BE pathogenesis and esophageal carcinogenesis.
中心性肥胖可通过机械和/或代谢机制(如高胰岛素血症)增加 Barrett 食管(BE)和食管腺癌的风险。我们进行了一项流行病学研究,以确定 2 型糖尿病(DM2)是否与 BE 相关。
我们使用英国初级保健数据库 General Practice Research Database 进行了一项基于人群的病例对照研究,该数据库包含超过 800 万受试者的信息,以确定 BE 病例(使用先前验证的代码;n=14245)和无 BE 的匹配对照(按年龄、性别、入组日期、随访评估时间和按发病率密度抽样的实践区域;n=70361)。我们使用条件单变量和多变量回归分析评估 DM2 既往诊断与 BE 的相关性。评估的混杂因素包括吸烟、体重指数(BMI)衡量的肥胖和胃食管反流病。
BE 病例比对照更有可能吸烟(52.4% vs 49.9%)、平均 BMI 更高(27.2 与 26.9)、DM2 患病率高于对照(5.8% vs 5.3%)。在多变量分析中,DM2 与 BE 风险增加 49%相关,独立于其他已知危险因素(比值比,1.49;95%置信区间,1.16-1.91)。这种关联在女性中比男性更强。敏感性分析结果稳定。
在一项大型基于人群的病例对照研究中,DM2 是 BE 的危险因素,与肥胖(BMI 衡量)和其他危险因素(吸烟和胃食管反流病)无关。这些数据表明,应在 BE 发病机制和食管癌变中探索与 DM2 相关的代谢途径。