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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Veröffentlicht in: | Basic & clinical pharmacology & toxicology 2017-02, Vol.120 (2), p.199-206 |
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Sprache: | eng |
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Zusammenfassung: | 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. |
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ISSN: | 1742-7835 1742-7843 |
DOI: | 10.1111/bcpt.12667 |