Protocol for a randomised 'screen-and-treat' Helicobacter pylori eradication trial in 14-18-years-old adolescents residing in three regions of Chile: effectiveness and microbiological host implications.

IF 2.3 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL BMJ Open Pub Date : 2025-01-30 DOI:10.1136/bmjopen-2024-084984
Sergio George, Yalda Lucero, Camila Cabrera, Beatriz Zabala Torres, Lilian Fernández, Nora Mamani, Anne Lagomarcino, Ximena Aguilera, Miguel O'Ryan
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Abstract

Introduction: Gastric cancer is a major global health concern, being the final stage of a long-term process, primarily associated with Helicobacter pylori (H. pylori) infection. Early childhood acquisition of H. pylori with low spontaneous eradication rates underscores the need for preventive measures. Our previous pilot treatment study revealed high eradication rates, favourable tolerance profile and a decline in serum biomarkers indicative of gastric damage in asymptomatic school-aged children. The purpose of this study is to determine the potential benefit of a 'screen-and-treat' strategy targeting persistently infected, asymptomatic adolescents. Specific aims are to assess eradication efficacy, its clinical and molecular outcomes and potential clinical and microbiological side effects.

Methods and analysis: The screening phase will involve testing 500-1000 asymptomatic adolescents aged 14-18 from three cities in Chile using the urea breath test (UBT) to identify 210 participants with persistent infection. They will proceed to a randomised, non-blinded, controlled trial, receiving either a sequential eradication scheme for H. pylori or no treatment. Follow-up will span up to 24 months post-treatment, involving UBT, gastroenterological assessments and blood and stool sample collections. Concurrently, a subset of 60 uninfected adolescents will undergo matched follow-up. Enzyme-linked immunosorbent assay (ELISA) commercial kits will evaluate gastric damage biomarkers in serum (pepsinogen I and II, gastrin-17, VCAM-1, CXCL13). Stool samples will be employed for Escherichia coli and Enterococcus spp-culture, assessing AMR via the disk diffusion method. H. pylori clarithromycin resistance will be determined by molecular method from stool samples. The gut microbiome will be characterised by amplifying and sequencing the 16S rRNA gene from stool samples, followed by bioinformatics analysis.

Ethics and dissemination: Approved by the Human Research Ethics Committee at the Faculty of Medicine, University of Chile (073-2022). Findings will be disseminated in peer-reviewed journals and scientific meetings to guide future practices.

Trial registration number: NCT05926804.

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在智利三个地区的14-18岁青少年中进行的随机“筛查和治疗”幽门螺杆菌根除试验方案:有效性和微生物宿主影响
导论:胃癌是一个主要的全球健康问题,是一个长期过程的最后阶段,主要与幽门螺杆菌(H. pylori)感染有关。儿童早期获得幽门螺杆菌,自发根除率低,强调需要采取预防措施。我们之前的试点治疗研究显示,在无症状学龄儿童中,高根除率、良好的耐受性和表明胃损伤的血清生物标志物下降。本研究的目的是确定针对持续感染的无症状青少年的“筛查和治疗”策略的潜在益处。具体目的是评估根除效果、临床和分子结果以及潜在的临床和微生物副作用。方法和分析:筛查阶段将包括使用尿素呼吸试验(UBT)对来自智利三个城市的500-1000名14-18岁无症状青少年进行检测,以确定210名持续感染的参与者。他们将进入一项随机、非盲、对照试验,要么接受幽门螺杆菌的顺序根除计划,要么不接受治疗。随访将在治疗后长达24个月,包括UBT、胃肠病学评估以及血液和粪便样本收集。同时,将对60名未感染青少年进行相应的随访。酶联免疫吸附试验(ELISA)商业化试剂盒将评估血清中的胃损伤生物标志物(胃蛋白酶原I和II、胃泌素-17、VCAM-1、CXCL13)。粪便样本将用于大肠杆菌和肠球菌的培养,通过圆盘扩散法评估AMR。采用分子法从粪便样品中检测幽门螺杆菌克拉霉素耐药性。肠道微生物组将通过从粪便样本中扩增和测序16S rRNA基因来表征,然后进行生物信息学分析。伦理与传播:经智利大学医学院人类研究伦理委员会批准(073-2022)。研究结果将在同行评议的期刊和科学会议上传播,以指导未来的实践。试验注册号:NCT05926804。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMJ Open
BMJ Open MEDICINE, GENERAL & INTERNAL-
CiteScore
4.40
自引率
3.40%
发文量
4510
审稿时长
2-3 weeks
期刊介绍: BMJ Open is an online, open access journal, dedicated to publishing medical research from all disciplines and therapeutic areas. The journal publishes all research study types, from study protocols to phase I trials to meta-analyses, including small or specialist studies. Publishing procedures are built around fully open peer review and continuous publication, publishing research online as soon as the article is ready.
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