Section of Gastroenterology and Hepatology, Department of Medicine, Michael E. DeBakey Veterans' Affairs Medical Center, Baylor College Medicine, Houston, Texas; Section of Health Services Research, Department of Medicine, Michael E. DeBakey Veterans' Affairs Medical Center, Baylor College Medicine, Houston, Texas.
Section of Gastroenterology and Hepatology, Department of Medicine, Michael E. DeBakey Veterans' Affairs Medical Center, Baylor College Medicine, Houston, Texas.
Gastroenterology. 2015 Nov;149(6):1392-8. doi: 10.1053/j.gastro.2015.07.009. Epub 2015 Jul 21.
BACKGROUND & AIMS: Statins have been reported to protect against esophageal adenocarcinoma (EAC) in patients with Barrett's esophagus (BE). However, there are few data from adequately powered cohort studies of subjects with BE.
We conducted a nested case-control study of a cohort of BE patients identified from national Veteran Affairs (VA) outpatient files, diagnosed with BE from 2004 through 2009. New cases of EAC recorded after BE diagnosis were identified during a follow-up period that ended in 2011 and verified using electronic medical records. We selected patients with BE without EAC (controls) using incidence density sampling; 3 controls were matched to each case based on birth year and date of BE diagnosis. Our analysis included only male patients with at least 1 VA visit per year of follow up. We identified prescriptions for statins and non-statin lipid lowering medications filled after BE diagnosis and up to 90 days before EAC diagnosis for cases and controls (during the corresponding time period); we examined the association between statin use and EAC in conditional logistic regression models.
We compared 311 EAC cases to 856 controls. Cases were less likely to use any statins than controls (40.2% vs 54.0%; P < .01). Significantly lower proportions of cases used statins for 6-18 months (10.0% cases vs 17.1% controls) and >18 months (19.3% vs 24.0%, respectively; P < .01). Simvastatin was the most commonly prescribed statin (accounting for 86.9% of statin use); the defined daily dose of simvastatin was lower in cases than in controls (21-40 mg/day, 9.3% vs 14.5%, respectively; and >40 mg/day, 8.4% vs 12.6%, respectively; P < .01). In multivariate analysis, statin use was inversely associated with development of EAC (adjusted odds ratio [OR], 0.65; 95% confidence interval [CI], 0.47-0.91). This protective association was strongest for patients with advanced-stage EAC: in a stratified analysis, comparison of 189 cases with stage 0-1 EAC to 520 controls produced an adjusted OR of 0.85 (95% CI, 0.54-1.33). Among patients with late-stage EAC (stages 2-4, n = 106) and 291 controls, the adjusted OR was 0.44 (95% CI, 0.25-0.79). We found no association between EAC and non-statin lipid-lowering medications.
In a case-control study of US veterans, statin use among those with BE appeared to decrease the risk of EAC. This protective effect was strongest against advanced-stage EAC, and increased with statin dose.
有报道称他汀类药物可预防 Barrett 食管(BE)患者的食管腺癌(EAC)。然而,来自于足够大的 BE 患者队列研究的数据较少。
我们对从美国退伍军人事务部(VA)门诊档案中确定的 BE 患者队列进行了嵌套病例对照研究,这些患者在 2004 年至 2009 年期间被诊断为 BE。在 2011 年结束的随访期间,记录了新诊断的 EAC 病例,并使用电子病历进行了验证。我们使用发病率密度抽样选择没有 EAC 的 BE 患者(对照);每例病例匹配了 3 例对照,匹配依据是出生年份和 BE 诊断日期。我们的分析仅包括每年至少有 1 次 VA 就诊的男性患者。我们确定了病例和对照在 BE 诊断后至 EAC 诊断前 90 天内(在相应时间段内)开具的他汀类药物和非他汀类降脂药物处方;我们使用条件逻辑回归模型检查了他汀类药物使用与 EAC 之间的关系。
我们将 311 例 EAC 病例与 856 例对照进行了比较。与对照相比,病例使用任何他汀类药物的可能性较低(40.2% vs 54.0%;P <.01)。使用他汀类药物 6-18 个月(10.0%的病例 vs 17.1%的对照)和 >18 个月(19.3%的病例 vs 24.0%的对照)的比例显著较低(P <.01)。辛伐他汀是最常用的他汀类药物(占他汀类药物使用的 86.9%);病例组的辛伐他汀日剂量定义低于对照组(21-40mg/天,9.3% vs 14.5%;和 >40mg/天,8.4% vs 12.6%;P <.01)。在多变量分析中,他汀类药物的使用与 EAC 的发生呈负相关(调整后的比值比[OR],0.65;95%置信区间[CI],0.47-0.91)。这种保护作用在 EAC 晚期患者中最强:在分层分析中,将 189 例 EAC 0-1 期患者与 520 例对照进行比较,调整后的 OR 为 0.85(95% CI,0.54-1.33)。在晚期 EAC(2-4 期,n = 106)患者和 291 例对照中,调整后的 OR 为 0.44(95% CI,0.25-0.79)。我们未发现 EAC 与非他汀类降脂药物之间存在关联。
在一项针对美国退伍军人的病例对照研究中,BE 患者使用他汀类药物似乎降低了 EAC 的风险。这种保护作用在 EAC 晚期最强,并随着他汀类药物剂量的增加而增加。