Waldum Helge L, Brenna Eiliv, Sandvik Arne K
Faculty of Medicine, Department of Intra-abdominal Diseases, Norwegian University of Science and Technology, Trondheim University Hospital, N-7006 Trondheim, Norway.
Expert Opin Drug Saf. 2002 May;1(1):29-38. doi: 10.1517/14740338.1.1.29.
After Helicobacter pylori eradication was introduced and largely eliminated the need for maintenance therapy for peptic ulcer disease, gastroesophageal reflux disease (GERD) became the main indication for prolonged gastric acid inhibition. The drug effect on GERD depends on the degree of acid inhibition, thus the efficacious proton pump inhibitors are preferred. The proton pump inhibitors have few immediate side effects, the main concern being the profound hypoacidity and hypergastrinaemia they induce. In short-term, hypergastrinaemia causes rebound hyperacidity, possibly worsening GERD and reducing the efficacy of histamine H(2) blockers. In the long-term, hypergastrinaemia causes enterochromaffin-like cell hyperplasia and carcinoids. Since enterochromaffin-like cells may be important in gastric carcinogenesis, iatrogenic hypergastrinaemia may predispose to carcinoma. Gastric hypoacidity also increases gut bacterial infections, and the barrier function of acid against viral and prion infections requires further assessment.
自从幽门螺杆菌根除疗法问世并在很大程度上消除了消化性溃疡疾病维持治疗的必要性后,胃食管反流病(GERD)成为长期胃酸抑制治疗的主要适应证。药物对GERD的疗效取决于抑酸程度,因此有效的质子泵抑制剂成为首选。质子泵抑制剂几乎没有即刻副作用,主要问题在于它们会引起严重的胃酸过少和高胃泌素血症。短期内,高胃泌素血症会导致胃酸分泌反跳性增加,可能使GERD恶化,并降低组胺H2受体阻滞剂的疗效。长期来看,高胃泌素血症会导致肠嗜铬样细胞增生和类癌。由于肠嗜铬样细胞可能在胃癌发生过程中起重要作用,医源性高胃泌素血症可能会诱发癌症。胃酸过少还会增加肠道细菌感染,而胃酸对病毒和朊病毒感染的屏障作用需要进一步评估。