Endoscopic analysis of gastric ulcer after one week's treatment with omeprazole and rabeprazole in relation to CYP2C19 genotype

被引:21
作者
Ando, Takashi [1 ]
Ishikawa, Takeshi [2 ]
Kokura, Satoshi [3 ]
Naito, Yuji [4 ]
Yoshida, Norimasa [5 ]
Yoshikawa, Toshikazu [6 ]
机构
[1] Social Insurance Kyoto Hosp, Div Gastroenterol, Kyoto 6038151, Japan
[2] Matsushita Mem Hosp, Dept Gastroenterol, Osaka, Japan
[3] Kyoto Prefectural Univ Med, Dept Biomed Safety Sci, Kyoto, Japan
[4] Kyoto Prefectural Univ Med, Dept Med Proteom, Kyoto, Japan
[5] Kyoto Prefectural Univ Med, Dept Mol gastroentelor & Hepatol, Kyoto, Japan
[6] Kyoto Prefectural Univ Med, Dept Inflammat & Immunol, Grad Sch Med Sci, Kyoto, Japan
关键词
rabeprazole; omeprazole; gastric ulcer; CYP2C19; endoscopy; mucosal repair;
D O I
10.1007/s10620-007-9965-3
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
In Japanese healthy CYP2C19 extensive metabolizers, rabeprazole 10 mg shows a faster onset of action and stronger inhibition of acid secretion than does omeprazole 20 mg on the first 3 days of administration. We evaluated gastric ulcer improvement after 1 week's treatment with rabeprazole or omeprazole in relation to CYP2C19 polymorphism. A 6-mm rubber disc was placed temporarily at the side of the ulcer for measurement of the ulcer area. The improvement ratios of ulcer area in homozygous extensive metabolizers (homoEMs), heterozygous extensive metabolizers (heteroEMs) and poor metabolizers (PMs) treated with rabeprazole 10 mg were 60.8, 65.0 and 55.3%, respectively, and these values are not significantly different. Corresponding values with omeprazole 20 mg were 46.3, 61.7 and 63.2%, respectively, and the value of homoEMs was significantly smaller than that of heteroEMs. The improvement ratios with rabeprazole in homoEMs and heteroEMs were significantly greater than that with omeprazole in homoEMs.
引用
收藏
页码:933 / 937
页数:5
相关论文
共 19 条
[1]   A comparative study on endoscopic ulcer healing of omeprazole versus rabeprazole with respect to CYP2C19 genotypic differences [J].
Ando, T ;
Kato, H ;
Sugimoto, N ;
Nagao, Y ;
Seto, N ;
Hongo, H ;
Kajikawa, H ;
Isozaki, Y ;
Shimozawa, M ;
Naito, Y ;
Yoshida, N ;
Ishizaki, T ;
Yoshikawa, T .
DIGESTIVE DISEASES AND SCIENCES, 2005, 50 (09) :1625-1631
[2]   IN-SITU HYBRIDIZATION OF MESSENGER-RNA FOR THE GASTRIC H+, K+-ATPASE IN RAT OXYNTIC MUCOSA [J].
BAMBERG, K ;
NYLANDER, S ;
HELANDER, KG ;
LUNDBERG, LG ;
SACHS, G ;
HELANDER, HF .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 1994, 1190 (02) :355-359
[3]   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
[4]   Altered expression of aquaporin 4 and H+/K+-ATPase in the stomachs of peptide YY (PYY) transgenic mice [J].
Carmosino, M ;
Mazzone, A ;
Laforenza, U ;
Gastaldi, G ;
Svelto, M ;
Valenti, G .
BIOLOGY OF THE CELL, 2005, 97 (09) :735-742
[5]  
DEMORAIS SMF, 1994, MOL PHARMACOL, V46, P594
[6]   Pharmacodynamic effects and kinetic disposition of rabeprazole in relation to CYP2C19 genotype in healthy Chinese subjects [J].
Hu, YM ;
Xu, JM ;
Mei, Q ;
Xu, XH ;
Xu, SY .
ACTA PHARMACOLOGICA SINICA, 2005, 26 (03) :384-388
[7]   Comparison of the effect on intragastric pH of a single dose of omeprazole or rabeprazole: Which is suitable for on-demand therapy? [J].
Inamori, M ;
Togawa, JI ;
Takahashi, H ;
Yoneda, M ;
Fujisawa, N ;
Iwasaki, T ;
Ozawa, Y ;
Kikuchi, T ;
Muramatsu, K ;
Chiguchi, G ;
Matsumoto, S ;
Kawamura, H ;
Abe, Y ;
Kirikoshi, H ;
Kobayashi, N ;
Sakaguchi, T ;
Takamura, T ;
Nakajima, A ;
Ueno, N ;
Sekihara, H .
JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2003, 18 (09) :1034-1038
[8]  
Ishizaki T, 1999, ALIMENT PHARM THERAP, V13, P27
[9]   Functional heterogeneity of parietal cells along the pit-gland axis [J].
Karam, SM ;
Yao, XB ;
Forte, JG .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 1997, 272 (01) :G161-G171
[10]   Genotyping of S-mephenytoin 4'-hydroxylation in an extended Japanese population [J].
Kubota, T ;
Chiba, K ;
Ishizaki, T .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 1996, 60 (06) :661-666