Esomeprazole 40 mg twice daily in triple therapy and the efficacy of Helicobacter pylori eradication related to CYP2C19 metabolism

Summary Aim : To determine whether an increased dosage of esomeprazole 40 mg twice daily in triple therapy improved the Helicobacter pylori eradication rate for patients with different genotypes of S‐mephenytoin 4′‐hydroxylase (CYP2C19). Methods : Two hundred H. pylori‐infected dyspeptic patients we...

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Veröffentlicht in:Alimentary pharmacology & therapeutics 2005-02, Vol.21 (3), p.283-288
Hauptverfasser: Sheu, B.‐S., Kao, A.‐W., Cheng, H.‐C., Hunag, S.‐F., Chen, T.‐W., Lu, C.‐C., Wu, J.‐J.
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container_end_page 288
container_issue 3
container_start_page 283
container_title Alimentary pharmacology & therapeutics
container_volume 21
creator Sheu, B.‐S.
Kao, A.‐W.
Cheng, H.‐C.
Hunag, S.‐F.
Chen, T.‐W.
Lu, C.‐C.
Wu, J.‐J.
description Summary Aim : To determine whether an increased dosage of esomeprazole 40 mg twice daily in triple therapy improved the Helicobacter pylori eradication rate for patients with different genotypes of S‐mephenytoin 4′‐hydroxylase (CYP2C19). Methods : Two hundred H. pylori‐infected dyspeptic patients were randomized to receive clarithromycin 500 mg twice daily and amoxicillin 1 g twice daily plus either omeprazole 20 mg or esomeprazole 40 mg twice daily for 1 week. Six weeks later, the success of H. pylori eradication was defined. The genotyping of CYP2C19 in each patient was defined as homologous, heterologous extensive metabolizer or poor metabolizer. Results : The age, gender, drug compliance and proportion of CYP2C19 genotypes were similar between the two groups. The H. pylori eradication rates were also similar between the omeprazole group and the esomeprazole group (intention‐to‐treat analysis: 79% vs. 86%, P > 0.05; per‐protocol analysis: 85% vs. 94%, P > 0.05). For patients classified as homologous extensive metabolizers, the per‐protocol H. pylori eradication rate was significantly higher in the esomeprazole group than in the omeprazole group (93% vs. 76%, P 
doi_str_mv 10.1111/j.1365-2036.2005.02281.x
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Methods : Two hundred H. pylori‐infected dyspeptic patients were randomized to receive clarithromycin 500 mg twice daily and amoxicillin 1 g twice daily plus either omeprazole 20 mg or esomeprazole 40 mg twice daily for 1 week. Six weeks later, the success of H. pylori eradication was defined. The genotyping of CYP2C19 in each patient was defined as homologous, heterologous extensive metabolizer or poor metabolizer. Results : The age, gender, drug compliance and proportion of CYP2C19 genotypes were similar between the two groups. The H. pylori eradication rates were also similar between the omeprazole group and the esomeprazole group (intention‐to‐treat analysis: 79% vs. 86%, P &gt; 0.05; per‐protocol analysis: 85% vs. 94%, P &gt; 0.05). For patients classified as homologous extensive metabolizers, the per‐protocol H. pylori eradication rate was significantly higher in the esomeprazole group than in the omeprazole group (93% vs. 76%, P &lt; 0.05). Conclusion : Esomeprazole 40 mg twice daily for triple therapy may improve the H. pylori eradication compared to omeprazole‐based therapy, but only for homologous extensive metabolizers of CYP2C19.</description><identifier>ISSN: 0269-2813</identifier><identifier>EISSN: 1365-2036</identifier><identifier>DOI: 10.1111/j.1365-2036.2005.02281.x</identifier><identifier>PMID: 15691303</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Science Ltd</publisher><subject>Adult ; Amoxicillin - administration &amp; dosage ; Amoxicillin - therapeutic use ; Anti-Bacterial Agents - therapeutic use ; Anti-Ulcer Agents - administration &amp; dosage ; Anti-Ulcer Agents - therapeutic use ; Aryl Hydrocarbon Hydroxylases - genetics ; Aryl Hydrocarbon Hydroxylases - metabolism ; Biological and medical sciences ; Chi-Square Distribution ; Clarithromycin - administration &amp; dosage ; Clarithromycin - therapeutic use ; Cytochrome P-450 CYP2C19 ; Digestive system ; Drug Administration Schedule ; Drug Therapy, Combination ; Esomeprazole ; Female ; Follow-Up Studies ; Gastric Mucosa - enzymology ; Gastroenterology. Liver. Pancreas. Abdomen ; Genotype ; Helicobacter Infections - drug therapy ; Helicobacter Infections - enzymology ; Helicobacter pylori ; Humans ; Male ; Medical sciences ; Mixed Function Oxygenases - genetics ; Mixed Function Oxygenases - metabolism ; Omeprazole - administration &amp; dosage ; Omeprazole - therapeutic use ; Pharmacology. 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Methods : Two hundred H. pylori‐infected dyspeptic patients were randomized to receive clarithromycin 500 mg twice daily and amoxicillin 1 g twice daily plus either omeprazole 20 mg or esomeprazole 40 mg twice daily for 1 week. Six weeks later, the success of H. pylori eradication was defined. The genotyping of CYP2C19 in each patient was defined as homologous, heterologous extensive metabolizer or poor metabolizer. Results : The age, gender, drug compliance and proportion of CYP2C19 genotypes were similar between the two groups. The H. pylori eradication rates were also similar between the omeprazole group and the esomeprazole group (intention‐to‐treat analysis: 79% vs. 86%, P &gt; 0.05; per‐protocol analysis: 85% vs. 94%, P &gt; 0.05). For patients classified as homologous extensive metabolizers, the per‐protocol H. pylori eradication rate was significantly higher in the esomeprazole group than in the omeprazole group (93% vs. 76%, P &lt; 0.05). Conclusion : Esomeprazole 40 mg twice daily for triple therapy may improve the H. pylori eradication compared to omeprazole‐based therapy, but only for homologous extensive metabolizers of CYP2C19.</description><subject>Adult</subject><subject>Amoxicillin - administration &amp; dosage</subject><subject>Amoxicillin - therapeutic use</subject><subject>Anti-Bacterial Agents - therapeutic use</subject><subject>Anti-Ulcer Agents - administration &amp; dosage</subject><subject>Anti-Ulcer Agents - therapeutic use</subject><subject>Aryl Hydrocarbon Hydroxylases - genetics</subject><subject>Aryl Hydrocarbon Hydroxylases - metabolism</subject><subject>Biological and medical sciences</subject><subject>Chi-Square Distribution</subject><subject>Clarithromycin - administration &amp; dosage</subject><subject>Clarithromycin - therapeutic use</subject><subject>Cytochrome P-450 CYP2C19</subject><subject>Digestive system</subject><subject>Drug Administration Schedule</subject><subject>Drug Therapy, Combination</subject><subject>Esomeprazole</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Gastric Mucosa - enzymology</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Genotype</subject><subject>Helicobacter Infections - drug therapy</subject><subject>Helicobacter Infections - enzymology</subject><subject>Helicobacter pylori</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Mixed Function Oxygenases - genetics</subject><subject>Mixed Function Oxygenases - metabolism</subject><subject>Omeprazole - administration &amp; dosage</subject><subject>Omeprazole - therapeutic use</subject><subject>Pharmacology. 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Liver. Pancreas. Abdomen</topic><topic>Genotype</topic><topic>Helicobacter Infections - drug therapy</topic><topic>Helicobacter Infections - enzymology</topic><topic>Helicobacter pylori</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Mixed Function Oxygenases - genetics</topic><topic>Mixed Function Oxygenases - metabolism</topic><topic>Omeprazole - administration &amp; dosage</topic><topic>Omeprazole - therapeutic use</topic><topic>Pharmacology. Drug treatments</topic><topic>Risk</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sheu, B.‐S.</creatorcontrib><creatorcontrib>Kao, A.‐W.</creatorcontrib><creatorcontrib>Cheng, H.‐C.</creatorcontrib><creatorcontrib>Hunag, S.‐F.</creatorcontrib><creatorcontrib>Chen, T.‐W.</creatorcontrib><creatorcontrib>Lu, C.‐C.</creatorcontrib><creatorcontrib>Wu, J.‐J.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Alimentary pharmacology &amp; therapeutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sheu, B.‐S.</au><au>Kao, A.‐W.</au><au>Cheng, H.‐C.</au><au>Hunag, S.‐F.</au><au>Chen, T.‐W.</au><au>Lu, C.‐C.</au><au>Wu, J.‐J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Esomeprazole 40 mg twice daily in triple therapy and the efficacy of Helicobacter pylori eradication related to CYP2C19 metabolism</atitle><jtitle>Alimentary pharmacology &amp; therapeutics</jtitle><addtitle>Aliment Pharmacol Ther</addtitle><date>2005-02</date><risdate>2005</risdate><volume>21</volume><issue>3</issue><spage>283</spage><epage>288</epage><pages>283-288</pages><issn>0269-2813</issn><eissn>1365-2036</eissn><abstract>Summary Aim : To determine whether an increased dosage of esomeprazole 40 mg twice daily in triple therapy improved the Helicobacter pylori eradication rate for patients with different genotypes of S‐mephenytoin 4′‐hydroxylase (CYP2C19). Methods : Two hundred H. pylori‐infected dyspeptic patients were randomized to receive clarithromycin 500 mg twice daily and amoxicillin 1 g twice daily plus either omeprazole 20 mg or esomeprazole 40 mg twice daily for 1 week. Six weeks later, the success of H. pylori eradication was defined. The genotyping of CYP2C19 in each patient was defined as homologous, heterologous extensive metabolizer or poor metabolizer. Results : The age, gender, drug compliance and proportion of CYP2C19 genotypes were similar between the two groups. The H. pylori eradication rates were also similar between the omeprazole group and the esomeprazole group (intention‐to‐treat analysis: 79% vs. 86%, P &gt; 0.05; per‐protocol analysis: 85% vs. 94%, P &gt; 0.05). For patients classified as homologous extensive metabolizers, the per‐protocol H. pylori eradication rate was significantly higher in the esomeprazole group than in the omeprazole group (93% vs. 76%, P &lt; 0.05). Conclusion : Esomeprazole 40 mg twice daily for triple therapy may improve the H. pylori eradication compared to omeprazole‐based therapy, but only for homologous extensive metabolizers of CYP2C19.</abstract><cop>Oxford, UK</cop><pub>Blackwell Science Ltd</pub><pmid>15691303</pmid><doi>10.1111/j.1365-2036.2005.02281.x</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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source Wiley Free Content; MEDLINE; IngentaConnect Free/Open Access Journals; Wiley Online Library Journals Frontfile Complete; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals
subjects Adult
Amoxicillin - administration & dosage
Amoxicillin - therapeutic use
Anti-Bacterial Agents - therapeutic use
Anti-Ulcer Agents - administration & dosage
Anti-Ulcer Agents - therapeutic use
Aryl Hydrocarbon Hydroxylases - genetics
Aryl Hydrocarbon Hydroxylases - metabolism
Biological and medical sciences
Chi-Square Distribution
Clarithromycin - administration & dosage
Clarithromycin - therapeutic use
Cytochrome P-450 CYP2C19
Digestive system
Drug Administration Schedule
Drug Therapy, Combination
Esomeprazole
Female
Follow-Up Studies
Gastric Mucosa - enzymology
Gastroenterology. Liver. Pancreas. Abdomen
Genotype
Helicobacter Infections - drug therapy
Helicobacter Infections - enzymology
Helicobacter pylori
Humans
Male
Medical sciences
Mixed Function Oxygenases - genetics
Mixed Function Oxygenases - metabolism
Omeprazole - administration & dosage
Omeprazole - therapeutic use
Pharmacology. Drug treatments
Risk
title Esomeprazole 40 mg twice daily in triple therapy and the efficacy of Helicobacter pylori eradication related to CYP2C19 metabolism
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