克拉霉素
甲硝唑
医学
幽门螺杆菌
阿莫西林
CYP2C19型
抗生素
药效学
抗菌剂
抗生素耐药性
四环素
抗菌剂
药理学
药代动力学
微生物学
内科学
生物
细胞色素P450
新陈代谢
作者
Takahisa Furuta,David Y. Graham
标识
DOI:10.1016/j.gtc.2010.08.007
摘要
The commonly used regimens for the eradication of Helicobacter pylori infection consist of administration of proton pump inhibitors (PPIs) and 1 to 3 antimicrobial agents, such as amoxicillin , clarithromycin , metronidazole , fluoroquinolone , or tetracycline . Each agent has its own pharmacologic characteristics. PPIs are metabolized by cytochrome P450 2C19 (CYP2C19), which is polymorphic. CYP2C19 genotypic differences in the pharmacokinetics and pharmacodynamics of PPIs influence the eradication rates of H pylori infection by PPI-containing regimens. Amoxicillin is a time-dependent antibiotic, whereas clarithromycin, metronidazole, tetracycline, and fluoroquinolone are not. The plasma half-life of antimicrobial agents also differs among these antibiotics. To achieve consistently high eradication rates, the eradication regimens must be designed based on a good understanding of the resistance patterns of the bacteria and the pharmacologic characteristics of the agents used for H pylori eradication therapy .
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