Houston Veterans Affairs Health Services Research and Development Center for Innovations in Quality, Effectiveness and Safety, Houston, Texas; Department of Medicine, Baylor College of Medicine, Houston, Texas; Department of Pathology, Baylor College of Medicine, Houston, Texas.
Department of Medicine, Baylor College of Medicine, Houston, Texas; Department of Pathology, Baylor College of Medicine, Houston, Texas.
Gastroenterology. 2014 Aug;147(2):314-23. doi: 10.1053/j.gastro.2014.04.040. Epub 2014 May 2.
BACKGROUND & AIMS: Statins have been associated with a reduced risk of esophageal adenocarcinoma, but little is known about their effect on development of Barrett's esophagus. We evaluated the association between statins and risk of Barrett's esophagus.
We conducted a case-control study among eligible patients scheduled for elective esophagogastroduodenoscopy and patients eligible for screening colonoscopy, recruited from primary care clinics at a Veterans Affairs center. We compared 303 patients with Barrett's esophagus with 2 separate sex-matched control groups: 606 elective endoscopy controls and 303 primary care controls without Barrett's esophagus. Use of statins and other lipid-lowering medications was ascertained by reviewing filled prescriptions in electronic pharmacy records during a 10-year period before the Barrett's esophagus diagnosis date for patients and study endoscopy date for controls. We calculated odds ratios (OR) and 95% confidence intervals (CI) using conditional multivariable logistic-regression models among 276 patients and 828 controls further matched on age.
A smaller proportion of Barrett's esophagus patients filled statin prescriptions (57.4%) than endoscopy controls (64.9%; P = .029) or primary care controls (71.3%; P < .001). Controls had longer durations of statin prescriptions filled than patients (28.6 vs 22.1 months; P = .001). Statin use was associated with a significantly lower risk of Barrett's esophagus (adjusted OR = 0.57; 95% CI: 0.38-0.87) compared with the combined control groups. The risk of Barrett's esophagus was especially lower with statin use among obese patients (OR = 0.26; 95% CI: 0.09-0.71), as was the risk for Barrett's esophagus segments ≥ 3 cm (OR = 0.13; 95% CI: 0.06-0.30). We found no significant association between Barrett's esophagus and nonstatin lipid-lowering medications (P = .452).
In a case-control study of veterans, statin use was associated with a reduced risk of Barrett's esophagus. The greatest level of risk reduction was observed for obese patients and for long-segment Barrett's esophagus.
他汀类药物已被证实与食管腺癌风险降低相关,但关于其对巴雷特食管发展的影响知之甚少。本研究旨在评估他汀类药物与巴雷特食管风险之间的关系。
我们对在退伍军人事务中心的初级保健诊所接受择期食管胃十二指肠镜检查的患者或有筛查结肠镜检查适应证的患者进行了病例对照研究。我们将 303 例巴雷特食管患者与 2 个独立的性别匹配对照组进行比较,即 606 例择期内镜对照组和 303 例无巴雷特食管的初级保健对照组。通过在巴雷特食管诊断日期之前的 10 年内在电子病历中查看患者的处方和对照研究的内镜日期,来确定他汀类药物和其他降脂药物的使用情况。我们在进一步匹配了年龄的 276 例患者和 828 例对照中,通过条件多变量逻辑回归模型计算了比值比(OR)和 95%置信区间(CI)。
与内镜对照组(64.9%;P =.029)或初级保健对照组(71.3%;P <.001)相比,较少的巴雷特食管患者(57.4%)服用他汀类药物。对照组的他汀类药物处方持续时间长于患者(28.6 个月比 22.1 个月;P =.001)。与合并对照组相比,使用他汀类药物与巴雷特食管的发生风险显著降低相关(调整 OR = 0.57;95%CI:0.38-0.87)。在肥胖患者中,他汀类药物的使用与巴雷特食管的发生风险降低尤其相关(OR = 0.26;95%CI:0.09-0.71),对于 3cm 以上的巴雷特食管节段也是如此(OR = 0.13;95%CI:0.06-0.30)。我们未发现巴雷特食管与非他汀类降脂药物之间存在显著相关性(P =.452)。
在一项退伍军人的病例对照研究中,他汀类药物的使用与巴雷特食管的发生风险降低相关。肥胖患者和长节段巴雷特食管患者的风险降低程度最大。