4.6 Article

Metabolic Syndrome as a Risk Factor for Barrett Esophagus: A Population-Based Case-Control Study

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MAYO CLINIC PROCEEDINGS
卷 88, 期 2, 页码 157-165

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ELSEVIER SCIENCE INC
DOI: 10.1016/j.mayocp.2012.09.017

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  1. American College of Gastroenterology
  2. National Institute of Diabetes and Digestive and Kidney Diseases [RC4DK090413]
  3. Mayo Foundation
  4. National Institute on Aging of the National Institutes of Health [R01AG034676]

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Objectives: To assess the association between Barrett esophagus (BE) and the metabolic syndrome in patients with and without reflux symptoms and to determine whether this association is reflux independent and metabolically driven. Patients and Methods: Case patients with BE and controls were residents of Olmsted County, Minnesota (1999-2006). Two control groups (one with and one without symptoms of gastroesophageal reflux) were identified from a cohort of patients who had responded to a validated gastrointestinal symptom questionnaire. Cases and controls were individually matched by age, sex, and duration of follow-up. Controls did not have a known diagnosis of BE. The association of the metabolic syndrome and its individual components with BE was assessed using univariate and multivariate conditional logistic regression separately for each control group. Results: A total of 309 patients were included (103 BE cases, 103 controls with reflux symptoms, and 103 controls without reflux symptoms). A total of 64% of cases, 47% of controls with reflux symptoms, and 50% of controls without reflux symptoms had the metabolic syndrome. The metabolic syndrome was associated with a 2-fold increased risk of BE relative to those with (odds ratio, 2.00; 95% CI, 1.10-3.65; P=.02) and without (odds ratio, 1.90; 95% CI, 1.03-3.60; P=.04) reflux symptoms. This association was independent of smoking, alcohol consumption, and body mass index and remained robust with sensitivity analysis. Conclusion: The metabolic syndrome is associated with BE independent of reflux symptoms, which may reflect a reflux-independent pathway of BE pathogenesis. (C) 2013 Mayo Foundation for Medical Education and Research square Mayo Clin Proc. 2013;88(2):157-165

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