elexacaftor/tezacaftor/ivacaftor 对囊性纤维化青少年口咽部元基因组的纵向影响。

IF 5.4 2区 医学 Q1 RESPIRATORY SYSTEM Journal of Cystic Fibrosis Pub Date : 2024-10-14 DOI:10.1016/j.jcf.2024.10.001
Ruth Steinberg, Alexander Moeller, Amanda Gisler, Nadja Mostacci, Markus Hilty, Jakob Usemann
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引用次数: 0

摘要

背景:三联调节疗法 elexacaftor/tezacaftor/ivacaftor (ETI) 可改善晚期肺病囊性纤维化患者(pwCF)的肺功能,并对呼吸道微生物群产生影响。然而,与成年囊性纤维化患者相比,青少年囊性纤维化患者的细菌病原体定植较少,但他们的微生物群已经与健康人不同。本研究旨在纵向分析 ETI 对以轻度 CF 肺病为主的青少年呼吸道元基因组的影响:在这项前瞻性观察研究中,我们纳入了年龄在 12-20 岁、至少有一个 F508del 基因突变的 pwCF,他们在开始接受 ETI 治疗前后收集了口咽拭子,在三个月内每周两次到每两周一次。我们进行了全元基因组枪式测序,然后进行了宿主 DNA 筛选和分类分析。我们使用线性和加性混合效应模型来研究微生物组的纵向发展,这些模型对已知的混杂因素进行了调整,并对多重测试进行了校正。我们分析了细菌的多样性、丰度和菌株级系统发育:结果:我们分析了 20 个 pwCF 的 297 份拭子的元基因组数据。微生物组的组成在接受 ETI 治疗后发生了变化。随着时间的推移,我们观察到微生物组略有多样化(Inv Simpson, Coef 0.085, 95 %CI 0.003, 0.17, p = 0.04)。菌株水平分析和聚类显示,即使在 ETI 治疗期间,最常见细菌种类的菌株保留率也很高:结论:在三个月的 ETI 治疗期间,共生菌增多,这可能有助于防止细菌病原体的过度生长。
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Longitudinal effects of elexacaftor/tezacaftor/ivacaftor on the oropharyngeal metagenome in adolescents with cystic fibrosis.

Background: Triple modulator therapy elexacaftor/tezacaftor/ivacaftor (ETI) improves lung function and impacts upon the respiratory microbiome in people with Cystic fibrosis (pwCF) with advanced lung disease. However, adolescents with cystic fibrosis (CF) are less colonized with bacterial pathogens than adult pwCF but their microbiota already differs from healthy individuals. The aim of this study was to longitudinally analyze the impact of ETI on the respiratory metagenome in adolescents with predominantly mild CF lung disease.

Methods: In this prospective observational study, we included pwCF aged 12-20 years with at least one F508del mutation, who collected oropharyngeal swabs before and after initiation of ETI therapy twice per week to biweekly over three months. We performed whole metagenome shotgun sequencing, followed by host DNA filtering and taxonomic profiling. We used linear and additive mixed effects models adjusted for known confounders and corrected for multiple testing to study longitudinal development of the microbiome. We analyzed bacterial diversity, abundance, and strain-level phylogeny.

Results: We analyzed the metagenomic data of 297 swabs of 20 pwCF. Microbiome composition changed after initiation of ETI therapy. We observed a slight diversification of the microbiome over time (Inv Simpson, Coef 0.085, 95 %CI 0.003, 0.17, p = 0.04). Strain-level analysis and clustering showed that strain retention of the most frequent bacterial species is predominant even during ETI therapy.

Conclusions: During three months of ETI therapy, commensal bacteria increased, which may help to prevent overgrowth of bacterial pathogens.

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来源期刊
Journal of Cystic Fibrosis
Journal of Cystic Fibrosis 医学-呼吸系统
CiteScore
10.10
自引率
13.50%
发文量
1361
审稿时长
50 days
期刊介绍: The Journal of Cystic Fibrosis is the official journal of the European Cystic Fibrosis Society. The journal is devoted to promoting the research and treatment of cystic fibrosis. To this end the journal publishes original scientific articles, editorials, case reports, short communications and other information relevant to cystic fibrosis. The journal also publishes news and articles concerning the activities and policies of the ECFS as well as those of other societies related the ECFS.
期刊最新文献
What does it mean to be "healthy" when taking elexacaftor/tezacaftor/ivacaftor (ETI)? A qualitative study. Process and validity of linking cystic fibrosis patient registry with national Medicaid databases. Characterization of 223 infants with CFTR-related metabolic syndrome/Cystic fibrosis screen positive, inconclusive diagnosis (CRMS/CFSPID) identified during the first three years of newborn screening via IRT-DNA-SEQ in New York State. A W1282X cystic fibrosis mouse allows the study of pharmacological and gene-editing therapeutics to restore CFTR function. Elexacaftor/tezacaftor/ivacaftor efficacy in intestinal organoids with rare CFTR variants in comparison to CFTR-F508del and CFTR-wild type controls.
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