Rates and predictors of progression to esophageal carcinoma in a large population-based Barrett's esophagus cohort

被引:44
作者
Krishnamoorthi, Rajesh [1 ]
Borah, Bijan [2 ]
Heien, Herbert [2 ]
Das, Ananya [3 ]
Chak, Amitabh [4 ]
Iyer, Prasad G. [1 ]
机构
[1] Mayo Clin, Div Gastroenterol & Hepatol, Rochester, MN 55905 USA
[2] Mayo Clin, Div Hlth Care Policy & Res, Rochester, MN 55905 USA
[3] Arizona Ctr Digest Hlth, Gilbert, AZ USA
[4] Case Western Reserve Univ, Div Gastroenterol & Hepatol, Cleveland, OH 44106 USA
关键词
NONSTEROIDAL ANTIINFLAMMATORY DRUGS; PROTON PUMP INHIBITORS; IMMORTAL TIME BIAS; NEOPLASTIC PROGRESSION; REDUCED RISK; INTESTINAL METAPLASIA; MALIGNANT PROGRESSION; COLUMNAR EPITHELIUM; CANCER-RISK; ADENOCARCINOMA;
D O I
10.1016/j.gie.2015.12.036
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background and Aims: Rates of progression to esophageal adenocarcinoma in subjects with Barrett's esophagus (BE) are lower than previously estimated. Identification of predictors of progression will enable risk stratification of BE subjects, potentially making current surveillance programs more efficient. We aimed to assess the potential of demographic and lifestyle factors, obesity, and medications in predicting progression in BE. Methods: BE subjects were identified from the General Practice Research Database using validated diagnostic codes. BE subjects developing esophageal cancer (EC) 12 months after their index BE diagnosis were defined as progressors. Time-to-event analysis was used to assess the overall risk of progression to EC. Cox proportional hazards models and time-varying marginal structural models were used to assess predictors of progression. Results: Included in the analysis were 9660 BE patients. The mean age (SD) of the study subjects was 63 (13.5) years; 62.6% were men. One hundred three subjects (1.1%) progressed to EC. The mean (SD) follow-up since initial diagnosis was 4.8 (3.3) years. The incidence of EC was 2.23 per 1000 person-years of follow-up. Increasing age, male gender, and being overweight (body mass index, 25-29.9) were found to be independent predictors of progression. When time-varying models were used, proton pump inhibitor (PPI) and statin use were protective against progression. Conclusions: In this large population-based cohort of patients with BE, increasing age, male gender, and being overweight predicted progression to EC, whereas PPI and statin use were protective against EC development. These factors may aid in developing a risk score to predict the risk of progression and chemopreventive strategies in patients with BE.
引用
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页码:40 / +
页数:14
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