Effect of esomeprazole and rabeprazole on intragastric pH in healthy Chinese: an open, randomized crossover trial
- PMID: 17565634
- DOI: 10.1111/j.1440-1746.2006.04709.x
Effect of esomeprazole and rabeprazole on intragastric pH in healthy Chinese: an open, randomized crossover trial
Abstract
Background and aim: Esomeprazole is the S-isomer of omeprazole, with a stronger acid suppressive effect than omeprazole. This open, randomized crossover study was designed to evaluate the effect of esomeprazole and another proton-pump inhibitor, rabeprazole, on intragastric pH in healthy Chinese.
Methods: Thirty-six healthy volunteers (26 men and 10 women, aged between 20 and 31 years) were enrolled. Subjects were given either esomeprazole 40 mg (n = 18) or rabeprazole 10 mg (n = 18) orally once daily for 5 days during the first dosing period, then the other medicine at the set dosage for the second dosing period. The two periods were separated by a 14-day washout phase. The doses were chosen according to the State Food and Drug Administration of China for the treatment of acid-related diseases. Intragastric pH was continuously monitored for 24 h on days 1 and 5 of each dosing period. CYP2C19 genotypes were analyzed to identify the extensive metabolizers (EM) and poor metabolizers (PM).
Results: The percentage of time with intragastric pH >4 was significantly higher (P < 0.001) in subjects receiving esomeprazole than in those receiving rabeprazole in the first 4 h after administration of the first dose (70.65% vs 44.87%), at 24 h on day 1 (73.7% vs 54.8%) and at 24 h on day 5 (84.2% vs 76.2%). The median intragastric pH was also higher in subjects receiving esomeprazole than in those receiving rabeprazole in the first 6 h, day 1 and day 5 (P <or= 0.001). The percentage of subjects with intragastric pH >4 for at least 16 h on day 1 (63.9% vs 33.3%) and on day 5 (88.9% vs 61.1%) was higher after administration of esomeprazole than after rabeprazole (both P < 0.05). On genotype analysis, 28 of the subjects were EM and eight were PM. Those who were PM tended to have a higher, albeit not statistically significant, percentage of time with intragastric pH >4 and the median 24-h intragastric pH than those who were EM. Both drugs were well tolerated.
Conclusions: Esomeprazole 40 mg orally once daily is more effective and faster in increasing intragastric pH than rabeprazole 10 mg orally once daily, and thus offers a potential for improved efficacy in acid-related diseases.
Similar articles
-
Intragastric acidity after switching from 5-day treatment with intravenous pantoprazole 40 mg/d to 5-day treatment with oral esomeprazole 40 mg/d or pantoprazole 40 mg/d: an open-label crossover study in healthy adult volunteers.Clin Ther. 2006 May;28(5):725-33. doi: 10.1016/j.clinthera.2006.05.001. Clin Ther. 2006. PMID: 16861094 Clinical Trial.
-
An open-label, parallel, multiple-dose study comparing the pharmacokinetics and gastric acid suppression of rabeprazole extended-release with esomeprazole 40 mg and rabeprazole delayed-release 20 mg in healthy volunteers.Aliment Pharmacol Ther. 2011 Apr;33(7):845-54. doi: 10.1111/j.1365-2036.2011.04580.x. Epub 2011 Jan 28. Aliment Pharmacol Ther. 2011. PMID: 21272047 Clinical Trial.
-
Gastric acid control with esomeprazole, lansoprazole, omeprazole, pantoprazole, and rabeprazole: a five-way crossover study.Am J Gastroenterol. 2003 Dec;98(12):2616-20. doi: 10.1111/j.1572-0241.2003.08783.x. Am J Gastroenterol. 2003. PMID: 14687806 Clinical Trial.
-
Clinical impact of CYP2C19 polymorphism on the action of proton pump inhibitors: a review of a special problem.Int J Clin Pharmacol Ther. 2006 Jul;44(7):297-302. doi: 10.5414/cpp44297. Int J Clin Pharmacol Ther. 2006. PMID: 16961157 Review.
-
Review article: gastric acidity--comparison of esomeprazole with other proton pump inhibitors.Aliment Pharmacol Ther. 2003 Feb;17 Suppl 1:10-5; discussion 16-7. doi: 10.1046/j.1365-2036.17.s1.3.x. Aliment Pharmacol Ther. 2003. PMID: 12614300 Review.
Cited by
-
Proton pump inhibitors: an update of their clinical use and pharmacokinetics.Eur J Clin Pharmacol. 2008 Oct;64(10):935-51. doi: 10.1007/s00228-008-0538-y. Epub 2008 Aug 5. Eur J Clin Pharmacol. 2008. PMID: 18679668 Review.
-
A Pharmacogenetics-Based Approach to Managing Gastroesophageal Reflux Disease: Current Perspectives and Future Steps.Pharmgenomics Pers Med. 2023 Jun 23;16:645-664. doi: 10.2147/PGPM.S371994. eCollection 2023. Pharmgenomics Pers Med. 2023. PMID: 37383676 Free PMC article. Review.
-
Inhibitory effects of intravenous lansoprazole 30 mg and pantoprazole 40 mg twice daily on intragastric acidity in healthy Chinese volunteers: a randomized, open-labeled, two-way crossover study.Med Sci Monit. 2012 Feb;18(2):CR125-130. doi: 10.12659/msm.882468. Med Sci Monit. 2012. PMID: 22293876 Free PMC article. Clinical Trial.
-
Esomeprazole: a review of its use in the management of gastric acid-related diseases in adults.Drugs. 2008;68(11):1571-607. doi: 10.2165/00003495-200868110-00009. Drugs. 2008. PMID: 18627213 Review.
-
Individualized therapy for gastroesophageal reflux disease: potential impact of pharmacogenetic testing based on CYP2C19.Mol Diagn Ther. 2012 Aug 1;16(4):223-34. doi: 10.1007/BF03262211. Mol Diagn Ther. 2012. PMID: 22873740 Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources