Effects of Genetic Polymorphisms of Cytochrome P450 Enzymes and MDR 1 Transporter on Pantoprazole Metabolism and Helicobacter pylori Eradication
Pantoprazole is a proton pump inhibitor that is commonly used in the treatment of peptic ulcer disease ( PUD ) and metabolized by cytochrome P450 ( CYP ) enzymes CYP 2C19 and CYP 3A4. Pantoprazole is a substrate for multi‐drug resistance protein 1 ( MDR 1). Single nucleotide polymorphisms ( SNP s) i...
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creator | Karaca, R Ozgur Kalkisim, Said Altinbas, Akif Kilincalp, Serta Yuksel, Ilhami Goktas, Mustafa T Yasar, Umit Bozkurt, Atilla Babaoglu, Melih O |
description | Pantoprazole is a proton pump inhibitor that is commonly used in the treatment of peptic ulcer disease (
PUD
) and metabolized by cytochrome P450 (
CYP
) enzymes
CYP
2C19 and
CYP
3A4. Pantoprazole is a substrate for multi‐drug resistance protein 1 (
MDR
1). Single nucleotide polymorphisms (
SNP
s) in
CYP
2C19
,
CYP
3A4
and
MDR
1
affect enzyme activity or gene expression of proteins and may alter plasma pantoprazole concentrations and treatment success in
PUD
. In this study, we aimed to investigate the association between genetic polymorphisms in
CYP
2C19
,
CYP
3A4
and
MDR
1
and pharmacokinetics of pantoprazole and therapeutic outcome in patients with either
Helicobacter pylori
‐associated [H.P.(+)]‐
PUD
or [H.P.(+)]‐gastritis. The plasma pantoprazole concentrations were determined by using an
HPLC
method at the third hour after a 40‐mg tablet of pantoprazole administration in 194 newly diagnosed patients with either [H.P.(+)]‐
PUD
or [H.P.(+)]‐gastritis. Genotyping was performed by using
PCR
‐
RFLP
and
DNA
sequencing. Among patients appearing for follow‐up examination (n = 105), the eradication rate for
H. pylori
was 82.8% (n = 87). The median pantoprazole plasma concentrations in poor metabolizers (
PM
), rapid metabolizers (
RM
) and ultrarapid metabolizers (
URM
) were 2.07, 1.69 and 1.28 μg/ml, respectively (
p
= 0.04).
CYP
3A4*1G
and
*22
polymorphisms did not affect plasma pantoprazole concentrations and
H. pylori
eradication rate. The
MDR
1 genetic polymorphisms did not affect plasma pantoprazole concentrations.
MDR
1 3435
CC
‐2677
GG
‐1236
CC
haplotype carriers had lower
H. pylori
eradication rate (60%) than the remaining subjects (84.9%) while the difference was not statistically significant (
p
= 0.07). In conclusion, while
CYP
2C19
genetic polymorphisms significantly affected plasma pantoprazole concentrations, polymorphisms of
CYP
2C19
,
CYP
3A4
and
MDR
1
did not affect
H. pylori
eradication rates. |
doi_str_mv | 10.1111/bcpt.12667 |
format | Article |
fullrecord | <record><control><sourceid>crossref</sourceid><recordid>TN_cdi_crossref_primary_10_1111_bcpt_12667</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>10_1111_bcpt_12667</sourcerecordid><originalsourceid>FETCH-LOGICAL-c767-fa23883f1048bdac99be9c4dc6f91494cc83e790428320b9a659706269923a5b3</originalsourceid><addsrcrecordid>eNo9kM1KAzEURoMoWKsbnyBrYWr-JpkspY6t0GKR7ockk9CRmWRIspk-hY9sW8W7uRe-757FAeARowU-zbM2Y15gwrm4AjMsGClExej1_03LW3CX0hdCRDCMZuC7ds6anGBwcGW9zZ2Bu9BPQ4jjoUvDJVhOOZhDDIOFO1YiWPvjNNgElW_h9vUTYriPyqcxxGwjDB7ulM9hjOoYegu3Nisd-hPs8rC2fWeCVubcHac-xA7WUbWdUbkL_h7cONUn-_C352D_Vu-X62LzsXpfvmwKI7gonCK0qqjDiFW6VUZKbaVhreFOYiaZMRW1QiJGKkqQloqXUiBOuJSEqlLTOXj6xZoYUorWNWPsBhWnBqPmrLI5q2wuKukPEipo6w</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Effects of Genetic Polymorphisms of Cytochrome P450 Enzymes and MDR 1 Transporter on Pantoprazole Metabolism and Helicobacter pylori Eradication</title><source>Wiley Online Library Journals Frontfile Complete</source><source>Alma/SFX Local Collection</source><creator>Karaca, R Ozgur ; Kalkisim, Said ; Altinbas, Akif ; Kilincalp, Serta ; Yuksel, Ilhami ; Goktas, Mustafa T ; Yasar, Umit ; Bozkurt, Atilla ; Babaoglu, Melih O</creator><creatorcontrib>Karaca, R Ozgur ; Kalkisim, Said ; Altinbas, Akif ; Kilincalp, Serta ; Yuksel, Ilhami ; Goktas, Mustafa T ; Yasar, Umit ; Bozkurt, Atilla ; Babaoglu, Melih O</creatorcontrib><description>Pantoprazole is a proton pump inhibitor that is commonly used in the treatment of peptic ulcer disease (
PUD
) and metabolized by cytochrome P450 (
CYP
) enzymes
CYP
2C19 and
CYP
3A4. Pantoprazole is a substrate for multi‐drug resistance protein 1 (
MDR
1). Single nucleotide polymorphisms (
SNP
s) in
CYP
2C19
,
CYP
3A4
and
MDR
1
affect enzyme activity or gene expression of proteins and may alter plasma pantoprazole concentrations and treatment success in
PUD
. In this study, we aimed to investigate the association between genetic polymorphisms in
CYP
2C19
,
CYP
3A4
and
MDR
1
and pharmacokinetics of pantoprazole and therapeutic outcome in patients with either
Helicobacter pylori
‐associated [H.P.(+)]‐
PUD
or [H.P.(+)]‐gastritis. The plasma pantoprazole concentrations were determined by using an
HPLC
method at the third hour after a 40‐mg tablet of pantoprazole administration in 194 newly diagnosed patients with either [H.P.(+)]‐
PUD
or [H.P.(+)]‐gastritis. Genotyping was performed by using
PCR
‐
RFLP
and
DNA
sequencing. Among patients appearing for follow‐up examination (n = 105), the eradication rate for
H. pylori
was 82.8% (n = 87). The median pantoprazole plasma concentrations in poor metabolizers (
PM
), rapid metabolizers (
RM
) and ultrarapid metabolizers (
URM
) were 2.07, 1.69 and 1.28 μg/ml, respectively (
p
= 0.04).
CYP
3A4*1G
and
*22
polymorphisms did not affect plasma pantoprazole concentrations and
H. pylori
eradication rate. The
MDR
1 genetic polymorphisms did not affect plasma pantoprazole concentrations.
MDR
1 3435
CC
‐2677
GG
‐1236
CC
haplotype carriers had lower
H. pylori
eradication rate (60%) than the remaining subjects (84.9%) while the difference was not statistically significant (
p
= 0.07). In conclusion, while
CYP
2C19
genetic polymorphisms significantly affected plasma pantoprazole concentrations, polymorphisms of
CYP
2C19
,
CYP
3A4
and
MDR
1
did not affect
H. pylori
eradication rates.</description><identifier>ISSN: 1742-7835</identifier><identifier>EISSN: 1742-7843</identifier><identifier>DOI: 10.1111/bcpt.12667</identifier><language>eng</language><ispartof>Basic & clinical pharmacology & toxicology, 2017-02, Vol.120 (2), p.199-206</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c767-fa23883f1048bdac99be9c4dc6f91494cc83e790428320b9a659706269923a5b3</citedby><cites>FETCH-LOGICAL-c767-fa23883f1048bdac99be9c4dc6f91494cc83e790428320b9a659706269923a5b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids></links><search><creatorcontrib>Karaca, R Ozgur</creatorcontrib><creatorcontrib>Kalkisim, Said</creatorcontrib><creatorcontrib>Altinbas, Akif</creatorcontrib><creatorcontrib>Kilincalp, Serta</creatorcontrib><creatorcontrib>Yuksel, Ilhami</creatorcontrib><creatorcontrib>Goktas, Mustafa T</creatorcontrib><creatorcontrib>Yasar, Umit</creatorcontrib><creatorcontrib>Bozkurt, Atilla</creatorcontrib><creatorcontrib>Babaoglu, Melih O</creatorcontrib><title>Effects of Genetic Polymorphisms of Cytochrome P450 Enzymes and MDR 1 Transporter on Pantoprazole Metabolism and Helicobacter pylori Eradication</title><title>Basic & clinical pharmacology & toxicology</title><description>Pantoprazole is a proton pump inhibitor that is commonly used in the treatment of peptic ulcer disease (
PUD
) and metabolized by cytochrome P450 (
CYP
) enzymes
CYP
2C19 and
CYP
3A4. Pantoprazole is a substrate for multi‐drug resistance protein 1 (
MDR
1). Single nucleotide polymorphisms (
SNP
s) in
CYP
2C19
,
CYP
3A4
and
MDR
1
affect enzyme activity or gene expression of proteins and may alter plasma pantoprazole concentrations and treatment success in
PUD
. In this study, we aimed to investigate the association between genetic polymorphisms in
CYP
2C19
,
CYP
3A4
and
MDR
1
and pharmacokinetics of pantoprazole and therapeutic outcome in patients with either
Helicobacter pylori
‐associated [H.P.(+)]‐
PUD
or [H.P.(+)]‐gastritis. The plasma pantoprazole concentrations were determined by using an
HPLC
method at the third hour after a 40‐mg tablet of pantoprazole administration in 194 newly diagnosed patients with either [H.P.(+)]‐
PUD
or [H.P.(+)]‐gastritis. Genotyping was performed by using
PCR
‐
RFLP
and
DNA
sequencing. Among patients appearing for follow‐up examination (n = 105), the eradication rate for
H. pylori
was 82.8% (n = 87). The median pantoprazole plasma concentrations in poor metabolizers (
PM
), rapid metabolizers (
RM
) and ultrarapid metabolizers (
URM
) were 2.07, 1.69 and 1.28 μg/ml, respectively (
p
= 0.04).
CYP
3A4*1G
and
*22
polymorphisms did not affect plasma pantoprazole concentrations and
H. pylori
eradication rate. The
MDR
1 genetic polymorphisms did not affect plasma pantoprazole concentrations.
MDR
1 3435
CC
‐2677
GG
‐1236
CC
haplotype carriers had lower
H. pylori
eradication rate (60%) than the remaining subjects (84.9%) while the difference was not statistically significant (
p
= 0.07). In conclusion, while
CYP
2C19
genetic polymorphisms significantly affected plasma pantoprazole concentrations, polymorphisms of
CYP
2C19
,
CYP
3A4
and
MDR
1
did not affect
H. pylori
eradication rates.</description><issn>1742-7835</issn><issn>1742-7843</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNo9kM1KAzEURoMoWKsbnyBrYWr-JpkspY6t0GKR7ockk9CRmWRIspk-hY9sW8W7uRe-757FAeARowU-zbM2Y15gwrm4AjMsGClExej1_03LW3CX0hdCRDCMZuC7ds6anGBwcGW9zZ2Bu9BPQ4jjoUvDJVhOOZhDDIOFO1YiWPvjNNgElW_h9vUTYriPyqcxxGwjDB7ulM9hjOoYegu3Nisd-hPs8rC2fWeCVubcHac-xA7WUbWdUbkL_h7cONUn-_C352D_Vu-X62LzsXpfvmwKI7gonCK0qqjDiFW6VUZKbaVhreFOYiaZMRW1QiJGKkqQloqXUiBOuJSEqlLTOXj6xZoYUorWNWPsBhWnBqPmrLI5q2wuKukPEipo6w</recordid><startdate>201702</startdate><enddate>201702</enddate><creator>Karaca, R Ozgur</creator><creator>Kalkisim, Said</creator><creator>Altinbas, Akif</creator><creator>Kilincalp, Serta</creator><creator>Yuksel, Ilhami</creator><creator>Goktas, Mustafa T</creator><creator>Yasar, Umit</creator><creator>Bozkurt, Atilla</creator><creator>Babaoglu, Melih O</creator><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>201702</creationdate><title>Effects of Genetic Polymorphisms of Cytochrome P450 Enzymes and MDR 1 Transporter on Pantoprazole Metabolism and Helicobacter pylori Eradication</title><author>Karaca, R Ozgur ; Kalkisim, Said ; Altinbas, Akif ; Kilincalp, Serta ; Yuksel, Ilhami ; Goktas, Mustafa T ; Yasar, Umit ; Bozkurt, Atilla ; Babaoglu, Melih O</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c767-fa23883f1048bdac99be9c4dc6f91494cc83e790428320b9a659706269923a5b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Karaca, R Ozgur</creatorcontrib><creatorcontrib>Kalkisim, Said</creatorcontrib><creatorcontrib>Altinbas, Akif</creatorcontrib><creatorcontrib>Kilincalp, Serta</creatorcontrib><creatorcontrib>Yuksel, Ilhami</creatorcontrib><creatorcontrib>Goktas, Mustafa T</creatorcontrib><creatorcontrib>Yasar, Umit</creatorcontrib><creatorcontrib>Bozkurt, Atilla</creatorcontrib><creatorcontrib>Babaoglu, Melih O</creatorcontrib><collection>CrossRef</collection><jtitle>Basic & clinical pharmacology & toxicology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Karaca, R Ozgur</au><au>Kalkisim, Said</au><au>Altinbas, Akif</au><au>Kilincalp, Serta</au><au>Yuksel, Ilhami</au><au>Goktas, Mustafa T</au><au>Yasar, Umit</au><au>Bozkurt, Atilla</au><au>Babaoglu, Melih O</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of Genetic Polymorphisms of Cytochrome P450 Enzymes and MDR 1 Transporter on Pantoprazole Metabolism and Helicobacter pylori Eradication</atitle><jtitle>Basic & clinical pharmacology & toxicology</jtitle><date>2017-02</date><risdate>2017</risdate><volume>120</volume><issue>2</issue><spage>199</spage><epage>206</epage><pages>199-206</pages><issn>1742-7835</issn><eissn>1742-7843</eissn><abstract>Pantoprazole is a proton pump inhibitor that is commonly used in the treatment of peptic ulcer disease (
PUD
) and metabolized by cytochrome P450 (
CYP
) enzymes
CYP
2C19 and
CYP
3A4. Pantoprazole is a substrate for multi‐drug resistance protein 1 (
MDR
1). Single nucleotide polymorphisms (
SNP
s) in
CYP
2C19
,
CYP
3A4
and
MDR
1
affect enzyme activity or gene expression of proteins and may alter plasma pantoprazole concentrations and treatment success in
PUD
. In this study, we aimed to investigate the association between genetic polymorphisms in
CYP
2C19
,
CYP
3A4
and
MDR
1
and pharmacokinetics of pantoprazole and therapeutic outcome in patients with either
Helicobacter pylori
‐associated [H.P.(+)]‐
PUD
or [H.P.(+)]‐gastritis. The plasma pantoprazole concentrations were determined by using an
HPLC
method at the third hour after a 40‐mg tablet of pantoprazole administration in 194 newly diagnosed patients with either [H.P.(+)]‐
PUD
or [H.P.(+)]‐gastritis. Genotyping was performed by using
PCR
‐
RFLP
and
DNA
sequencing. Among patients appearing for follow‐up examination (n = 105), the eradication rate for
H. pylori
was 82.8% (n = 87). The median pantoprazole plasma concentrations in poor metabolizers (
PM
), rapid metabolizers (
RM
) and ultrarapid metabolizers (
URM
) were 2.07, 1.69 and 1.28 μg/ml, respectively (
p
= 0.04).
CYP
3A4*1G
and
*22
polymorphisms did not affect plasma pantoprazole concentrations and
H. pylori
eradication rate. The
MDR
1 genetic polymorphisms did not affect plasma pantoprazole concentrations.
MDR
1 3435
CC
‐2677
GG
‐1236
CC
haplotype carriers had lower
H. pylori
eradication rate (60%) than the remaining subjects (84.9%) while the difference was not statistically significant (
p
= 0.07). In conclusion, while
CYP
2C19
genetic polymorphisms significantly affected plasma pantoprazole concentrations, polymorphisms of
CYP
2C19
,
CYP
3A4
and
MDR
1
did not affect
H. pylori
eradication rates.</abstract><doi>10.1111/bcpt.12667</doi><tpages>8</tpages></addata></record> |
fulltext | fulltext |
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language | eng |
recordid | cdi_crossref_primary_10_1111_bcpt_12667 |
source | Wiley Online Library Journals Frontfile Complete; Alma/SFX Local Collection |
title | Effects of Genetic Polymorphisms of Cytochrome P450 Enzymes and MDR 1 Transporter on Pantoprazole Metabolism and Helicobacter pylori Eradication |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-26T21%3A05%3A20IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-crossref&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Effects%20of%20Genetic%20Polymorphisms%20of%20Cytochrome%20P450%20Enzymes%20and%20MDR%201%20Transporter%20on%20Pantoprazole%20Metabolism%20and%20Helicobacter%20pylori%20Eradication&rft.jtitle=Basic%20&%20clinical%20pharmacology%20&%20toxicology&rft.au=Karaca,%20R%20Ozgur&rft.date=2017-02&rft.volume=120&rft.issue=2&rft.spage=199&rft.epage=206&rft.pages=199-206&rft.issn=1742-7835&rft.eissn=1742-7843&rft_id=info:doi/10.1111/bcpt.12667&rft_dat=%3Ccrossref%3E10_1111_bcpt_12667%3C/crossref%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |