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质子泵抑制剂有此问题:替戈拉赞会影响胃排空并产生消化不良症状吗?

PPIs Have It: Does Tegoprazan Affect Gastric Emptying and Produce Dyspeptic Symptoms?

作者信息

Remes-Troche José María

机构信息

Laboratorio de Fisiología Digestiva y Motilidad Gastrointestinal, Instituto de Investigaciones Médico-Biológicas, Universidad Veracruzana, Iturbide s/n entre Carmen Serdán y 20 de Noviembre, col. Centro, Veracruz, Veracruz, Mexico.

出版信息

Dig Dis Sci. 2025 Apr;70(4):1283-1285. doi: 10.1007/s10620-025-08857-8. Epub 2025 Feb 19.

DOI:10.1007/s10620-025-08857-8
PMID:39971829
Abstract

The potassium-competitive acid blockers (P-CABs) are a novel class of potent antisecretory drugs that unlike the proton pump inhibitors (PPIs) are not dependent on activated proton pumps, acting near maximally from the first dose, a pharmacokinetic advantage over PPIs. Tegoprazan, a novel P-CAB, offers potent and rapid acid suppression without delaying gastric emptying, distinguishing it from PPIs. This commentary contextualizes these results within the broader landscape of functional dyspepsia management, highlighting the potential benefits of tegoprazan in patients requiring antisecretory therapy, emphasizing the need for further research into its long-term impacts on motility, gut microbiota composition, and symptomatology. This analysis underscores how P-CABs may redefine antisecretory therapies.

摘要

钾离子竞争性酸阻滞剂(P-CABs)是一类新型强效抗分泌药物,与质子泵抑制剂(PPIs)不同,它们不依赖于激活的质子泵,从首剂起就能近乎最大程度地发挥作用,这是相对于PPIs的药代动力学优势。替戈拉赞是一种新型P-CAB,能强效快速抑制胃酸分泌且不延迟胃排空,这使其有别于PPIs。本述评将这些结果置于功能性消化不良管理的更广阔背景中,强调替戈拉赞在需要抗分泌治疗的患者中的潜在益处,强调有必要进一步研究其对动力、肠道微生物群组成和症状学的长期影响。该分析强调了P-CABs如何可能重新定义抗分泌治疗。

相似文献

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PPIs Have It: Does Tegoprazan Affect Gastric Emptying and Produce Dyspeptic Symptoms?质子泵抑制剂有此问题:替戈拉赞会影响胃排空并产生消化不良症状吗?
Dig Dis Sci. 2025 Apr;70(4):1283-1285. doi: 10.1007/s10620-025-08857-8. Epub 2025 Feb 19.
2
Effects of Tegoprazan, Potassium-Competitive Acid Blocker, on the Gastric Emptying and Postprandial Symptoms in Healthy Humans.钾离子竞争性酸阻滞剂替戈拉赞对健康人胃排空及餐后症状的影响。
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Br J Clin Pharmacol. 2022 Jul;88(7):3288-3296. doi: 10.1111/bcp.15268. Epub 2022 Feb 23.

本文引用的文献

1
Efficacy of Tegoprazan in Patients With Functional Dyspepsia: A Prospective, Multicenter, Single-arm Study.替戈拉赞治疗功能性消化不良患者的疗效:一项前瞻性、多中心、单臂研究。
J Neurogastroenterol Motil. 2024 Jul 30;30(3):313-321. doi: 10.5056/jnm23150. Epub 2024 May 4.
2
Incidence of Small Intestinal Bacterial Overgrowth and Symptoms After 7 Days of Proton Pump Inhibitor Use: A Study on Healthy Volunteers.质子泵抑制剂使用 7 天后小肠细菌过度生长和症状的发生率:一项健康志愿者研究。
Dig Dis Sci. 2024 Jan;69(1):209-215. doi: 10.1007/s10620-023-08162-2. Epub 2023 Nov 1.
3
Prevalence of small intestinal bacterial overgrowth in patients with gastroparesis: a systematic review and meta-analysis.
胃轻瘫患者小肠细菌过度生长的患病率:一项系统评价和荟萃分析。
Gastroenterol Hepatol Bed Bench. 2023;16(1):438-447. doi: 10.22037/ghfbb.v16i1.2652.
4
Vonoprazan Therapy is as Effective for Functional Dyspepsia without Heartburn as Acotiamide Therapy.Vonoprazan 治疗功能性消化不良(无烧心症状)的疗效与 Acotiamide 相当。
J Gastrointestin Liver Dis. 2023 Mar 31;32(1):23-29. doi: 10.15403/jgld-4837.
5
Administration of a standard dose of vonoprazan fumarate delays gastric emptying in Japanese healthy adults: a prospective clinical trial.标准剂量富马酸沃克索拉唑对日本健康成年人胃排空有延迟作用:一项前瞻性临床试验。
J Gastroenterol. 2021 Aug;56(8):722-731. doi: 10.1007/s00535-021-01801-3. Epub 2021 Jun 22.
6
Functional Dyspepsia - A Revolution in Management.功能性消化不良——管理上的一场革命。
Am J Gastroenterol. 2018 Oct;113(10):1420-1422. doi: 10.1038/s41395-018-0264-8. Epub 2018 Sep 4.
7
Tegoprazan, a Novel Potassium-Competitive Acid Blocker to Control Gastric Acid Secretion and Motility.替戈拉赞,一种新型钾离子竞争性酸阻滞剂,用于控制胃酸分泌和运动。
J Pharmacol Exp Ther. 2018 Feb;364(2):275-286. doi: 10.1124/jpet.117.244202. Epub 2017 Nov 27.
8
Effects of proton pump inhibitors on gastric emptying: a systematic review.质子泵抑制剂对胃排空的影响:系统评价。
Dig Dis Sci. 2010 Sep;55(9):2431-40. doi: 10.1007/s10620-009-1076-x. Epub 2009 Dec 10.
9
Generation of dyspeptic symptoms by direct acid infusion into the stomach of healthy Japanese subjects.通过直接向健康日本受试者的胃内注入酸来诱发消化不良症状。
Aliment Pharmacol Ther. 2007 Jul 15;26(2):257-64. doi: 10.1111/j.1365-2036.2007.03367.x.