Department of Pharmacology, Pomeranian Medical University, Powstancow Wlkp. 72, 70-111, Szczecin, Poland.
Eur J Clin Pharmacol. 2010 Jul;66(7):681-7. doi: 10.1007/s00228-010-0818-1. Epub 2010 Apr 8.
Eradication of H. pylori is an important treatment strategy in peptic ulcer patients. Current regimens of eradication consist of proton pump inhibitor (PPI) and two antibiotics. Effects of PPI may depend on their metabolism, and other factors important for the pathophysiology of peptic ulcer disease. Aim of the present study was to evaluate an association of CYP2C19, MDR1, and IL-1B polymorphisms with the eradication rate of H. pylori in Polish Caucasian patients treated with a triple therapy of pantoprazole, amoxicillin, and metronidazole.
A total of 139 peptic ulcer patients, positive for H. pylori infection, were treated with triple therapy (pantoprazole + amoxicillin + metronidazole). Subsequently, the patients were divided into two groups (group 1, success, and group 2, failure of eradication after therapy) and genotyped by the PCR-RFLP method for the presence of CYP2C19 variant alleles (*2, *3, and *17), and MDR1 3435C>T and IL-1B +3954C>T polymorphisms. Pantoprazole serum concentrations were measured using the HPLC method.
No significant differences in frequency or distribution of CYP2C19 genotypes were found between the two groups of patients (i.e., with successful H. pylori eradication and treatment failure). However, any carrier of defective CYP2C192/2 genotype was found among patients with treatment failure. Similarly, MDR1 and IL-1B genotypes were found to be significantly associated with the success or failure of H. pylori eradication. Univariate and multivariate analysis of the genotypes did not reveal any significant association between the genotypes and H. pylori eradication. Pantoprazole concentrations differed significantly, and were the highest in patients with defective allele CYP2C192 carriers and lowest in hyperactive genotype homozygotes CYP2C1917/*17.
The results suggest that the CYP2C19 genotype contrary to MDR1 and IL-1B genotypes may have an impact on the efficacy of H. pylori eradication in peptic ulcer patients treated with pantoprazole in Polish Caucasian peptic ulcer patients administered pantoprazole, amoxicillin, and metronidazole.
根除幽门螺杆菌是消化性溃疡患者的重要治疗策略。目前的根除方案包括质子泵抑制剂(PPI)和两种抗生素。PPI 的作用可能取决于其代谢和其他对消化性溃疡病病理生理学有重要影响的因素。本研究旨在评估 CYP2C19、MDR1 和 IL-1B 多态性与波兰白种人患者接受泮托拉唑、阿莫西林和甲硝唑三联疗法根除幽门螺杆菌的根除率之间的关系。
对 139 例幽门螺杆菌感染阳性的消化性溃疡患者进行三联疗法(泮托拉唑+阿莫西林+甲硝唑)治疗。随后,将患者分为两组(组 1 为成功组,组 2 为治疗后根除失败组),并通过 PCR-RFLP 法检测 CYP2C19 变异等位基因(*2、3 和17)、MDR1 3435C>T 和 IL-1B+3954C>T 多态性。采用 HPLC 法测定泮托拉唑的血清浓度。
两组患者(即幽门螺杆菌根除成功组和治疗失败组)之间 CYP2C19 基因型的频率或分布无显著差异。然而,在治疗失败的患者中发现任何携带缺陷 CYP2C192/2 基因型的患者。同样,MDR1 和 IL-1B 基因型与幽门螺杆菌的根除成功或失败显著相关。基因型的单因素和多因素分析未显示基因型与幽门螺杆菌根除之间存在任何显著关联。泮托拉唑浓度差异显著,携带缺陷 CYP2C192 等位基因的患者浓度最高,CYP2C1917/*17 纯合子活性最高。
结果表明,在波兰白种人消化性溃疡患者中,CYP2C19 基因型与 MDR1 和 IL-1B 基因型相反,可能对接受泮托拉唑治疗的消化性溃疡患者的幽门螺杆菌根除疗效有影响。