• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

质子泵抑制剂维持治疗期间CYP2C19基因多态性对反流性食管炎复发的影响。

Influences of CYP2C19 polymorphism on recurrence of reflux esophagitis during proton pump inhibitor maintenance therapy.

作者信息

Saitoh Toshihito, Otsuka Hiroko, Kawasaki Takahiro, Endo Hitoshi, Iga Daijirou, Tomimatsu Masahiko, Fukushima Yasushi, Katsube Takao, Ogawa Kenji, Otsuka Kuniaki

机构信息

Department of Internal Medicine, Tokyo Women's Medical University, Medical Center East, Tokyo, Japan.

出版信息

Hepatogastroenterology. 2009 May-Jun;56(91-92):703-6.

PMID:19621685
Abstract

BACKGROUND/AIMS: Patients with erosive gastroesophageal reflux disease (GERD) have rapid recurrence after treatment withdrawal. The aim is to study the influences of CYP2C19 polymorphism on recurrence of GERD during proton pump inhibitor maintenance therapy.

METHODOLOGY

Ninety-nine patients with initial healing of GERD (judged by endoscopy) after 8 wk of treatment with PPIs were enrolled into maintenance therapy for 6 mo with rabeprazole (10 mg/day), omeprazole (20 mg/day) or lansoprazole (15 mg/day). The recurrence of GERD symptoms in the maintenance therapy was assessed by a QUEST questionnaire.

RESULTS

The recurrence rate of GERD symptoms in the group of CYP2C19 homozygous extensive metabolizers (38.5%) was significantly greater than those in groups of heterozygous extensive metabolizers (10.9%) and poor metabolizers (5.6%). The recurrence rates in patients treated with omeprazole (25%) and lansoprazole (30.8%) were significantly greater than that with rabeprazole (4.4%). The gender, age and H. pylori did not significantly affect the rate.

CONCLUSIONS

The CYP2C19 genotypes affected the recurrence rate of GERD symptoms during PPI maintenance therapy. The reason for the low recurrence rate with 10 mg/day rabeprazole possibly is due to its sufficient acid suppression independent of CYP2C19 genotypes in Japanese patients.

摘要

背景/目的:糜烂性胃食管反流病(GERD)患者在停药后易快速复发。目的是研究CYP2C19基因多态性对质子泵抑制剂维持治疗期间GERD复发的影响。

方法

99例在接受质子泵抑制剂(PPIs)治疗8周后初次愈合(通过内镜检查判断)的GERD患者,采用雷贝拉唑(10毫克/天)、奥美拉唑(20毫克/天)或兰索拉唑(15毫克/天)进行6个月的维持治疗。通过QUEST问卷评估维持治疗期间GERD症状的复发情况。

结果

CYP2C19纯合子广泛代谢者组的GERD症状复发率(38.5%)显著高于杂合子广泛代谢者组(10.9%)和慢代谢者组(5.6%)。接受奥美拉唑(25%)和兰索拉唑(30.8%)治疗的患者复发率显著高于接受雷贝拉唑(4.4%)治疗的患者。性别、年龄和幽门螺杆菌对复发率无显著影响。

结论

CYP2C19基因分型影响PPI维持治疗期间GERD症状的复发率。日本患者中10毫克/天雷贝拉唑复发率低的原因可能是其抑酸作用充分,且不受CYP2C19基因分型影响。

相似文献

1
Influences of CYP2C19 polymorphism on recurrence of reflux esophagitis during proton pump inhibitor maintenance therapy.质子泵抑制剂维持治疗期间CYP2C19基因多态性对反流性食管炎复发的影响。
Hepatogastroenterology. 2009 May-Jun;56(91-92):703-6.
2
Role of cytochrome P450 2C19 genetic polymorphisms in the therapeutic efficacy of omeprazole in Iranian patients with erosive reflux esophagitis.细胞色素 P450 2C19 基因多态性在伊朗糜烂性反流性食管炎患者奥美拉唑治疗疗效中的作用。
Arch Iran Med. 2010 Sep;13(5):406-12.
3
Characteristics of refractory gastroesophageal reflux disease (GERD) symptoms -is switching proton pump inhibitors based on the patient's CYP2C19 genotype an effective management strategy?难治性胃食管反流病(GERD)症状的特征——基于患者细胞色素P450 2C19(CYP2C19)基因型更换质子泵抑制剂是否为一种有效的管理策略?
Intern Med. 2015;54(2):97-105. doi: 10.2169/internalmedicine.54.3412. Epub 2015 Jan 15.
4
Influence of cytochrome P450 2C19 genetic polymorphism and dosage of rabeprazole on accuracy of proton-pump inhibitor testing in Chinese patients with gastroesophageal reflux disease.细胞色素P450 2C19基因多态性及雷贝拉唑剂量对中国胃食管反流病患者质子泵抑制剂检测准确性的影响
J Gastroenterol Hepatol. 2007 Aug;22(8):1286-92. doi: 10.1111/j.1440-1746.2007.04942.x. Epub 2007 Jun 7.
5
CYP2C19 genotype is associated with symptomatic recurrence of GERD during maintenance therapy with low-dose lansoprazole.CYP2C19基因分型与低剂量兰索拉唑维持治疗期间胃食管反流病的症状复发有关。
Eur J Clin Pharmacol. 2009 Jul;65(7):693-8. doi: 10.1007/s00228-009-0628-5. Epub 2009 Mar 4.
6
Factors associated with residual gastroesophageal reflux disease symptoms in patients receiving proton pump inhibitor maintenance therapy.接受质子泵抑制剂维持治疗的患者中与残留胃食管反流病症状相关的因素。
World J Gastroenterol. 2017 Mar 21;23(11):2060-2067. doi: 10.3748/wjg.v23.i11.2060.
7
The effects of lansoprazole on erosive reflux oesophagitis are influenced by CYP2C19 polymorphism.兰索拉唑对糜烂性反流性食管炎的疗效受细胞色素P450 2C19基因多态性的影响。
Aliment Pharmacol Ther. 2003 Apr 1;17(7):965-73. doi: 10.1046/j.1365-2036.2003.01539.x.
8
Randomized open trial for comparison of proton pump inhibitors in triple therapy for Helicobacter pylori infection in relation to CYP2C19 genotype.关于CYP2C19基因型,质子泵抑制剂在幽门螺杆菌感染三联疗法中的比较:一项随机开放试验
J Gastroenterol Hepatol. 2002 Jul;17(7):748-53. doi: 10.1046/j.1440-1746.2002.02790.x.
9
Review article: relationship between the metabolism and efficacy of proton pump inhibitors--focus on rabeprazole.综述文章:质子泵抑制剂的代谢与疗效之间的关系——聚焦雷贝拉唑
Aliment Pharmacol Ther. 2004 Nov;20 Suppl 6:11-9. doi: 10.1111/j.1365-2036.2004.02161.x.
10
Clinical impact of CYP2C19 polymorphism on the action of proton pump inhibitors: a review of a special problem.CYP2C19基因多态性对质子泵抑制剂作用的临床影响:一个特殊问题的综述
Int J Clin Pharmacol Ther. 2006 Jul;44(7):297-302. doi: 10.5414/cpp44297.

引用本文的文献

1
Cost-Utility Analysis of CYP2C19 Genotype Detection for Selection of Acid-Suppressive Therapy with Lansoprazole or Vonoprazan for Patients with Reflux Esophagitis in China.中国反流性食管炎患者应用兰索拉唑或沃诺拉赞进行抑酸治疗时 CYP2C19 基因型检测的成本-效用分析。
Clin Drug Investig. 2022 Oct;42(10):839-851. doi: 10.1007/s40261-022-01188-w. Epub 2022 Aug 22.
2
Pharmacogenomics fail to explain proton pump inhibitor refractory esophagitis in pediatric esophageal atresia.药物基因组学未能解释儿科食管闭锁中质子泵抑制剂难治性食管炎。
Neurogastroenterol Motil. 2022 Jan;34(1):e14217. doi: 10.1111/nmo.14217. Epub 2021 Aug 1.
3
Challenges and lessons learned from clinical pharmacogenetic implementation of multiple gene-drug pairs across ambulatory care settings.
从多个基因-药物组合在门诊环境中的临床药物遗传学实施中获得的挑战和经验教训。
Genet Med. 2019 Oct;21(10):2264-2274. doi: 10.1038/s41436-019-0500-7. Epub 2019 Mar 30.
4
Proton pump inhibitors: from CYP2C19 pharmacogenetics to precision medicine.质子泵抑制剂:从 CYP2C19 药物遗传学到精准医学。
Expert Opin Drug Metab Toxicol. 2018 Apr;14(4):447-460. doi: 10.1080/17425255.2018.1461835. Epub 2018 Apr 12.
5
A review of medical therapy for proton pump inhibitor nonresponsive gastroesophageal reflux disease.质子泵抑制剂无反应性胃食管反流病的药物治疗综述
Dis Esophagus. 2017 Sep 1;30(9):1-15. doi: 10.1093/dote/dox055.
6
Gastrointestinal symptoms associated with gastroesophageal reflux disease, and their relapses after treatment with proton pump inhibitors: A systematic review.与胃食管反流病相关的胃肠道症状及其质子泵抑制剂治疗后的复发:一项系统综述。
Electron Physician. 2017 Jun 25;9(6):4597-4605. doi: 10.19082/4597. eCollection 2017 Jun.
7
Maintenance therapy of gastroesophageal reflux disease.胃食管反流病的维持治疗
Clin J Gastroenterol. 2010 Apr;3(2):61-8. doi: 10.1007/s12328-010-0139-z. Epub 2010 Feb 19.
8
Genetic polymorphisms of CYP2C19 and IL1B have no influence on esomeprazole treatment for mild erosive esophagitis.CYP2C19和IL1B的基因多态性对艾司奥美拉唑治疗轻度糜烂性食管炎没有影响。
Kaohsiung J Med Sci. 2015 May;31(5):255-9. doi: 10.1016/j.kjms.2015.01.006. Epub 2015 Mar 10.
9
Individualized therapy for gastroesophageal reflux disease: potential impact of pharmacogenetic testing based on CYP2C19.基于 CYP2C19 的个体化治疗胃食管反流病:药物遗传学检测的潜在影响。
Mol Diagn Ther. 2012 Aug 1;16(4):223-34. doi: 10.1007/BF03262211.
10
The role of pharmacogenetics in nonmalignant gastrointestinal diseases.药物遗传学在非恶性胃肠道疾病中的作用。
Nat Rev Gastroenterol Hepatol. 2012 Feb 7;9(3):173-84. doi: 10.1038/nrgastro.2012.2.