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＜博士論文＞
NSAIDs起因性小腸粘膜傷害に対するPPIの作用と薬剤代謝酵素遺伝子多型との関連の検討
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| 概要 | BACKGROUND:Simultaneous use of proton pump inhibitors (PPIs) has been shown to increase the risk of nonsteroidal anti-inflammatory drug (NSAID)-induced small bowel injury. AIM:To investigate whether po...lymorphisms of the cytochrome P450 2C19 gene (CYP2C19), encoding a key metabolising enzyme for PPIs, are associated with small bowel injury induced by celecoxib in combination with the PPI rabeprazole. METHODS:Study participants included 55 healthy Japanese volunteers, who participated in the PPI-NSAID Kyushu University Study using video capsule endoscopy. For 2 weeks, 26 subjects were treated with celecoxib plus rabeprazole (rabeprazole group), and 29 subjects received celecoxib plus placebo (placebo group). All subjects were genotyped for CYP2C19 using real-time fluorescent polymerase chain reaction. Subjects were sub-classified as poor metabolizers or extensive metabolizers. The incidence and number of small bowel injuries were compared between poor metabolizers and extensive metabolizers in each group. RESULTS:In the rabeprazole group, the incidence of small bowel injuries was significantly higher in poor metabolizers than in extensive metabolizers (85.7% vs 31.6%, P=.026). The number of mucosal injuries in the rabeprazole group was also significantly higher in poor metabolizers compared with extensive metabolizers (median [range] 3 [0-31] vs 0 [0-7], P=.01). In addition, we found a significant interaction between CYP2C19 genotype and concomitant use of rabeprazole in subjects at risk for celecoxib-induced small bowel injury. CONCLUSIONS:The CYP2C19 genotype might be associated with the risk of small bowel injury when celecoxib is combined with rabeprazole.続きを見る |
本文ファイル
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med3134_abstract
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108 KB | 464 | 要旨 | |
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med3134_summary
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108 KB | 177 | 要約 | |
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med3134_review
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171 KB | 215 | 審査結果要旨 |
詳細
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| 登録日 | 2018.05.30 |
| 更新日 | 2018.08.31 |