CYP2C19 genotypes in the pharmacokinetics/pharmacodynamics of proton pump inhibitor-based therapy of Helicobacter pylori infection

被引:45
作者
Yang, Jyh-Chin [2 ,3 ]
Lin, Chun-Jung [1 ]
机构
[1] Natl Taiwan Univ, Sch Pharm, Coll Med, Taipei 100, Taiwan
[2] Natl Taiwan Univ, Hosp Med, Dept Internal Med, Taipei 100, Taiwan
[3] Natl Taiwan Univ, Coll Med, Dept Internal Med, Taipei 100, Taiwan
关键词
CYP2C19 genetic polymorphisms; eradication therapy; Helicobacter pylori; pharmacokinetic-pharmacodynamic; proton pump inhibitor; MEPHENYTOIN HYDROXYLATION DEFICIENCY; UNIDENTIFIED CURVED BACILLI; S-MEPHENYTOIN; TRIPLE THERAPY; ACID SUPPRESSION; DUAL THERAPY; CURE RATES; IN-VITRO; FUNCTIONAL-CHARACTERIZATION; GASTROINTESTINAL DISORDERS;
D O I
10.1517/17425250903386251
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
importance of the field. Proton pump inhibitors (PPIs) are potent gastric acid inhibitors. Therapies with a PPI and antibiotics are used to cure Helicobacter pylori (H. pylori) infection, which is closely related to many gastrointestinal diseases. Most PPIs are mainly metabolized by cytochrome 2C19 (CYP2C19). The genetic polymorphisms of CYP2C19 may lead to the differences in pharmacokinetics (PK), pharmacodynamics (PD) and clinical efficacy of PPIs. Areas covered in this review. The roles of PPIs on the eradication of H. pylori are summarized. The impact f CYP2C19 polymorphism on the PK and PD of PPIS is addressed and related to the present status of therapy for H. pylori infection. The opinions on the strategy of PPIs-based therapies of H. pylori infection are provided. What the reader will gain: Update the factors that may influence the PPIs-based therapies of H. pylori infection. Take home message: The eradication rates of H. pylori infection are significantly different between patients who are CYP2C19 extensive metabolizers and poor metabolizers, partly because of the differences in the PK and PD of PPIs. Nonetheless, the differences can be improved by adjusting the regimens of PPIs and using antibiotics that have less H. pylori-resistance.
引用
收藏
页码:29 / 41
页数:13
相关论文
共 118 条
[1]  
Äbelö A, 2000, DRUG METAB DISPOS, V28, P966
[2]   Pharmacokinetics and effect an caffeine metabolism of the proton pump inhibitors, omeprazole, lansoprazole, and pantoprazole [J].
Andersson, T ;
Holmberg, J ;
Röhss, K ;
Walan, A .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 1998, 45 (04) :369-375
[3]   Pharmacokinetic studies with esomeprazole, the (S)-isomer of omeprazole [J].
Andersson, T ;
Hassan-Alin, M ;
Hasselgren, G ;
Röhss, K ;
Weidolf, L .
CLINICAL PHARMACOKINETICS, 2001, 40 (06) :411-426
[4]   Gastric Acid Suppression by Proton Pump Inhibitors as a Risk Factor for Clostridium difficile-Associated Diarrhea in Hospitalized Patients [J].
Aseeri, Mohammed ;
Schroeder, Todd ;
Kramer, Joan ;
Zackula, Rosalee .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2008, 103 (09) :2308-2313
[5]   In vitro post-antibiotic effect of fluoroquinolones, macrolides, β-lactams, tetracyclines, vancomycin, clindamycin, linezolid, chloramphenicol, quinupristin/dalfopristin and rifampicin on Bacillus anthracis [J].
Athamna, A ;
Athamna, M ;
Medlej, B ;
Bast, DJ ;
Rubinstein, E .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2004, 53 (04) :609-615
[6]   Review article:: rabeprazole-based therapy in Helicobacter pylori eradication [J].
Barth, J ;
Hahne, W .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2002, 16 :31-33
[7]   Comparison of five antisecretory agents acting via gastric H+/K+-ATPase [J].
Bastaki, SMA ;
Chandranath, I ;
Garner, A .
JOURNAL OF PHYSIOLOGY-PARIS, 2000, 94 (01) :19-23
[8]   DOUBLE-BLIND TRIAL OF OMEPRAZOLE AND AMOXICILLIN TO CURE HELICOBACTER-PYLORI INFECTION IN PATIENTS WITH DUODENAL-ULCERS [J].
BAYERDORFFER, E ;
MIEHLKE, S ;
MANNES, GA ;
SOMMER, A ;
HOCHTER, W ;
WEINGART, J ;
HELDWEIN, W ;
KLANN, H ;
SIMON, T ;
SCHMITT, W ;
BASTLEIN, E ;
EIMILLER, A ;
HATZ, R ;
LEHN, N ;
DIRSCHEDL, P ;
STOLTE, M .
GASTROENTEROLOGY, 1995, 108 (05) :1412-1417
[9]   PRONOUNCED DIFFERENCES BETWEEN NATIVE CHINESE AND SWEDISH POPULATIONS IN THE POLYMORPHIC HYDROXYLATIONS OF DEBRISOQUIN AND S-MEPHENYTOIN [J].
BERTILSSON, L ;
LOU, YQ ;
DU, YL ;
LIU, Y ;
KUANG, TY ;
LIAO, XM ;
WANG, KY ;
REVIRIEGO, J ;
ISELIUS, L ;
SJOQVIST, F .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 1992, 51 (04) :388-397
[10]   Sites of reaction of the gastric H,K-ATPase with extracytoplasmic thiol reagents [J].
Besancon, M ;
Simon, A ;
Sachs, G ;
Shin, JM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (36) :22438-22446