Division of Gastroenterology, Rabin Medical Center, Petah Tikva, Israel.
Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.
United European Gastroenterol J. 2021 Apr;9(3):343-353. doi: 10.1177/2050640620951403. Epub 2021 Mar 18.
Gastric intestinal metaplasia is a pre-cancerous condition associated with multiple factors.
We evaluated whether cumulative proton pump inhibitor dose is associated with the diagnosis of gastric intestinal metaplasia while controlling for multiple variables.
We retrospectively identified patients who underwent upper endoscopy with gastric biopsy between 2005 and 2014. Covariate data retrieved included age, sex, ethnicity, smoking status, Helicobacter pylori status (based on clarithromycin-amoxicillin-proton pump inhibitor issued), cumulative proton pump inhibitor issued within 10 years (quartiles [PPI-Q ] of daily drug dose), anti-parietal cell antibodies, body mass index and comorbidity index.
Of the 14,147 included patients (median age 63.4 years; women 54.4%; Helicobacter pylori-positive 29.0%), 1244 (8.8%) had gastric intestinal metaplasia. Increasing age, Helicobacter pylori infection, smoking, anti-parietal cell antibodies and proton pump inhibitor use were all associated with the diagnosis of gastric intestinal metaplasia. Upper quartiles of cumulative proton pump inhibitor doses (PPI-Q and PPI-Q vs. PPI-Q ) were associated with the diagnosis of gastric intestinal metaplasia: adjusted odds ratios 1.32 (95% confidence interval [CI] 1.111.57) and 1.27 (95% CI 1.07-1.52), respectively, for the whole cohort (P 0.007, P 0.013), 1.69 (95% CI 1.23-2.33) and 1.40 (95% CI 1.04-1.89), respectively, for Helicobacter pylori-positive patients (P 0.004, P 0.005) and 1.21 (95% CI 0.98-1.49) and 1.20 (95% CI 0.96-1.49), respectively, for Helicobacter pylori-negative patients (P 0.288, P 0.018). Upper quartiles of proton pump inhibitor dose were associated with a 5-10-fold increased risk of low-grade dysplasia.
Among Helicobacter pylori-positive patients, proton pump inhibitor use appears to be associated with a dose-dependent increased likelihood of gastric intestinal metaplasia.
胃肠上皮化生是一种与多种因素相关的癌前病变。
我们评估了质子泵抑制剂累积剂量是否与胃肠上皮化生的诊断相关,同时控制了多个变量。
我们回顾性地确定了 2005 年至 2014 年间接受上消化道内镜检查和胃活检的患者。检索到的协变量数据包括年龄、性别、种族、吸烟状况、幽门螺杆菌状态(基于克拉霉素-阿莫西林-质子泵抑制剂的发放)、10 年内累积质子泵抑制剂发放量(质子泵抑制剂每日剂量四分位[PPI-Q])、壁细胞抗体、体重指数和合并症指数。
在纳入的 14147 例患者中(中位年龄 63.4 岁;女性 54.4%;幽门螺杆菌阳性 29.0%),1244 例(8.8%)患有胃肠上皮化生。年龄增长、幽门螺杆菌感染、吸烟、壁细胞抗体和质子泵抑制剂的使用均与胃肠上皮化生的诊断相关。累积质子泵抑制剂剂量的上四分位数(PPI-Q 和 PPI-Q 与 PPI-Q )与胃肠上皮化生的诊断相关:整个队列的调整后比值比分别为 1.32(95%置信区间[CI] 1.111.57)和 1.27(95% CI 1.07-1.52)(P 0.007,P 0.013),幽门螺杆菌阳性患者分别为 1.69(95% CI 1.23-2.33)和 1.40(95% CI 1.04-1.89)(P 0.004,P 0.005),幽门螺杆菌阴性患者分别为 1.21(95% CI 0.98-1.49)和 1.20(95% CI 0.96-1.49)(P 0.288,P 0.018)。质子泵抑制剂剂量的上四分位数与低级别异型增生的风险增加 5-10 倍相关。
在幽门螺杆菌阳性患者中,质子泵抑制剂的使用似乎与剂量相关的胃肠上皮化生的可能性增加有关。