Dojo M, Azuma T, Saito T, Ohtani M, Muramatsu A, Kuriyama M
Second Department of Internal Medicine, Fukui Medical University, Japan.
Dig Liver Dis. 2001 Nov;33(8):671-5. doi: 10.1016/s1590-8658(01)80043-8.
Omeprazole is mainly metabolized by cytochrome P450 2C19 (CYP2C19) in the liver. Rabeprazole, on the other hand, is mainly metabolized to thioether-rabeprazole via a non-enzymatic pathway and partially metabolized to demethylated-rabeprazole by CYP2C19 in liver CYP2C19 status may affect cure rate for Helicobacter pylori infection with proton pump inhibitor triple therapy.
To investigate whether genetic polymorphism of CYP2C19 and selected proton pump inhibitors (omeprazole or rabeprazole) were associated with cure rate for Helicobacter pylori infection using triple therapy with omeprazole or rabeprazole, amoxicillin, and clarithromycin.
A total of 170 Helicobacter pylori-positive patients with chronic gastritis were randomized to receive one of the following Helicobacter pylori eradication regimens; OAC (omeprazole 20 mg bd, amoxycillin 750 mg bd and clarithromycin 400 mg bd for 1 week) and RAC (rabeprazole 20 mg bd, amoxycillin 750 mg bd and clarithromycin 400 mg bd for 1 week). The CYP2C19 genotype; wild-type or two mutant genes (ml in exon 5 and m2 in exon 4), or both, were identified by polymerase chain reaction-restriction fragment length polymorphism.
In DAC regimen, cure rate (per protocol analysis) was 73.3% in homozygous extensive metabolizers, 86.1% in heterozygous extensive metabolizers, and 85.0% in poor metabolizers. In RAC regimen, the cure rate was 81.0% in homozygous extensive metabolizers, 82.9% in heterozygous extensive metabolizers, and 87.5% in poor metabolizers. Cure rate was not significantly different between the CYP2C19 genotypes in both regimens.
Triple therapy with proton pump inhibitor (omeprazole or rabeprazole), amoxycillin, and clarithromycin is sufficiently effective in cure of Helicobacter pylori infection regardless of CYP2C19 status.
奥美拉唑主要在肝脏中由细胞色素P450 2C19(CYP2C19)代谢。另一方面,雷贝拉唑主要通过非酶途径代谢为硫醚-雷贝拉唑,并在肝脏中由CYP2C19部分代谢为去甲基雷贝拉唑。CYP2C19状态可能会影响质子泵抑制剂三联疗法治疗幽门螺杆菌感染的治愈率。
研究CYP2C19基因多态性以及所选质子泵抑制剂(奥美拉唑或雷贝拉唑)与使用奥美拉唑或雷贝拉唑、阿莫西林和克拉霉素三联疗法治疗幽门螺杆菌感染的治愈率是否相关。
总共170例幽门螺杆菌阳性的慢性胃炎患者被随机分配接受以下幽门螺杆菌根除方案之一:OAC(奥美拉唑20毫克,每日两次,阿莫西林750毫克,每日两次,克拉霉素400毫克,每日两次,共1周)和RAC(雷贝拉唑20毫克,每日两次,阿莫西林750毫克,每日两次,克拉霉素400毫克,每日两次,共1周)。通过聚合酶链反应-限制性片段长度多态性鉴定CYP2C19基因型;野生型或两个突变基因(外显子5中的m1和外显子4中的m2),或两者。
在OAC方案中,纯合子广泛代谢者的治愈率(按方案分析)为73.3%,杂合子广泛代谢者为86.1%,代谢不良者为85.0%。在RAC方案中,纯合子广泛代谢者的治愈率为81.0%,杂合子广泛代谢者为82.9%,代谢不良者为87.5%。两种方案中CYP2C19基因型之间的治愈率无显著差异。
无论CYP2C19状态如何,质子泵抑制剂(奥美拉唑或雷贝拉唑)、阿莫西林和克拉霉素三联疗法治疗幽门螺杆菌感染均具有足够的疗效。