George Sergio, Lucero Yalda, Cabrera Camila, Zabala Torres Beatriz, Fernández Lilian, Mamani Nora, Lagomarcino Anne, Aguilera Ximena, O'Ryan Miguel
Department of Pediatrics and Pediatric Surgery (Eastern Campus), Luis Calvo Mackenna Hospital, Faculty of Medicine, Universidad de Chile, Santiago de Chile, Chile.
Department of Pediatrics and Pediatric Surgery (Northern Campus), Dr. Roberto del Río Hospital, Faculty of Medicine, Universidad de Chile, Santiago de Chile, Chile.
BMJ Open. 2025 Jan 30;15(1):e084984. doi: 10.1136/bmjopen-2024-084984.
Gastric cancer is a major global health concern, being the final stage of a long-term process, primarily associated with () infection. Early childhood acquisition of 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.
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 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 and spp-culture, assessing AMR via the disk diffusion method. 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.
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.
NCT05926804.
胃癌是全球主要的健康问题,是一个长期过程的最终阶段,主要与()感染有关。儿童早期感染且自发清除率低凸显了采取预防措施的必要性。我们之前的试点治疗研究显示,在无症状学龄儿童中根除率高、耐受性良好,且表明胃损伤的血清生物标志物有所下降。本研究的目的是确定针对持续感染的无症状青少年的“筛查与治疗”策略的潜在益处。具体目标是评估根除效果、其临床和分子结果以及潜在的临床和微生物学副作用。
筛查阶段将涉及使用尿素呼气试验(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,以识别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,接受针对()的序贯根除方案或不接受治疗。随访将持续至治疗后24个月,包括UBT、胃肠病学评估以及血液和粪便样本采集。同时,60名未感染的青少年子集将进行匹配随访。酶联免疫吸附测定(ELISA)商业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、血管细胞黏附分子 - 1、CXC趋化因子配体13)。粪便样本将用于()和()菌种培养,通过纸片扩散法评估抗菌药物耐药性。粪便样本中的克拉霉素耐药性将通过分子方法确定。肠道微生物群将通过对粪便样本中的16S rRNA基因进行扩增和测序来表征,随后进行生物信息学分析。
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审期刊和科学会议上发表,以指导未来的实践。
NCT05926804。