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胃食管反流病患者服用雷贝拉唑8周后的血浆浓度及胃内pH值升高情况。

Plasma concentration of rabeprazole after 8-week administration in gastroesophageal reflux disease patients and intragastric pH elevation.

作者信息

Yamano Hiro-o, Matsushita Hiro-o, Yanagiwara Seiko

机构信息

Department of Gastroenterology, Akita Red Cross Hospital, Akita, Japan.

出版信息

J Gastroenterol Hepatol. 2008 Apr;23(4):534-40. doi: 10.1111/j.1440-1746.2007.05104.x. Epub 2007 Aug 27.

Abstract

BACKGROUND AND AIM

The plasma concentration of rabeprazole in patients treated for gastroesophageal reflux disease (GERD) has not been reported, although the concentration in healthy volunteers has been reported previously. Here, CYP2C19 genotype effects of rabeprazole on the area under the plasma concentration-time curve (AUC) and the pH elevation were studied in GERD patients.

METHODS

Rabeprazole 10 mg/day was administrated for 8 weeks. AUC of rabeprazole in 18 Helicobacter pylori-negative GERD subjects (five CYP2C19 homozygous extensive metabolizers [homEM], eight heterozygous extensive metabolizers [hetEM] and five poor metabolizers [PM]) were determined after the final medication. Intragastric pH was recorded for 24 h at baseline and after the final medication.

RESULTS

The AUC in the PM group (957 ng x h/mL) was significantly higher than those of homEM (375 ng x h/mL) and hetEM (542 ng x h/mL) groups. Median 24-h pH curves, median 24-h pH values and 24-h and nocturnal pH > 4 and pH > 3 holding times did not significantly differ among these groups. Disappearance of erosive lesions was observed after the treatment in all subjects with grade A, B or C at baseline irrespective of CYP2C19 genotypes.

CONCLUSION

The AUC of rabeprazole depended on the CYP2C19 genotypes in Japanese GERD patients; however, the intragastric pH elevation was independent of CYP2C19 genotypes, which is consistent with the CYP2C19 genotype-independent healing efficacy of erosive lesions by rabeprazole. The present low AUC values indicated that abnormal accumulative effects on AUC did not occur during the period of the 8-week administration of rabeprazole.

摘要

背景与目的

尽管先前已有关于健康志愿者中雷贝拉唑血浆浓度的报道,但尚未有针对胃食管反流病(GERD)患者的相关报道。在此,我们研究了雷贝拉唑的CYP2C19基因型对GERD患者血浆浓度-时间曲线下面积(AUC)及胃内pH升高的影响。

方法

每日服用10mg雷贝拉唑,持续8周。在18名幽门螺杆菌阴性的GERD受试者(5名CYP2C19纯合子广泛代谢者[纯合EM]、8名杂合子广泛代谢者[杂合EM]和5名慢代谢者[PM])中,在末次用药后测定雷贝拉唑的AUC。在基线期和末次用药后记录24小时胃内pH值。

结果

PM组的AUC(957 ng·h/mL)显著高于纯合EM组(375 ng·h/mL)和杂合EM组(542 ng·h/mL)。这些组之间的24小时pH曲线中位数、24小时pH值中位数以及24小时和夜间pH>4及pH>3的持续时间无显著差异。无论CYP2C19基因型如何,所有基线期为A、B或C级的受试者在治疗后糜烂性病变均消失。

结论

在日本GERD患者中,雷贝拉唑的AUC取决于CYP2C19基因型;然而,胃内pH升高与CYP2C19基因型无关,这与雷贝拉唑对糜烂性病变的CYP基因型独立愈合疗效一致。目前较低的AUC值表明,在雷贝拉唑8周给药期间未出现对AUC的异常累积效应。

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