Department of Pediatrics, University of Oklahoma School of Community Medicine, Tulsa, OK.
J Pediatr Gastroenterol Nutr. 2021 May 1;72(5):697-699. doi: 10.1097/MPG.0000000000003082.
Since the approval of the first proton pump inhibitor (PPI) in 1989, our knowledge regarding this class of medications has further developed. An increasing amount of data now supports the association between cytochrome P450 2C19 (CYP2C19) phenotype and PPI safety and efficacy. This includes pediatric studies, such as those published here and in other pediatric journals within the past year. Moreover, the most recent pediatric Helicobacter pylori guidelines stated that using the PPIs that are less dependent on CYP2C19 for inactivation may be preferred for H pylori eradication among populations that are more likely to have rapid clearance of CYP2C19-metabolized PPIs. Conversely, pantoprazole package insert recommends a dose reduction in known pediatric CYP2C19 poor metabolizers (PMs), citing a 6-fold increase in serum concentrations compared with normal metabolizers (NMs). The purpose of this communication is to introduce a recently published Clinical Pharmacogenetics Implementation Consortium (CPIC) guideline for CYP2C19 and PPI dosing.
自 1989 年批准首个质子泵抑制剂 (PPI) 以来,我们对这类药物的认识进一步发展。越来越多的数据现在支持细胞色素 P450 2C19(CYP2C19)表型与 PPI 安全性和疗效之间的关联。这包括儿科研究,例如这里和过去一年中其他儿科期刊上发表的研究。此外,最近的儿科幽门螺杆菌指南指出,对于 CYP2C19 代谢物清除较快的人群,使用对 CYP2C19 失活依赖性较小的 PPIs 可能更有利于幽门螺杆菌的根除。相反,泮托拉唑说明书建议在已知的儿科 CYP2C19 弱代谢者 (PM) 中减少剂量,与正常代谢者 (NM) 相比,血清浓度增加了 6 倍。本通讯的目的是介绍最近发布的细胞色素 P450 2C19 和 PPI 剂量的临床药物遗传学实施联盟 (CPIC) 指南。