Applied Sciences, Northumbria University Faculty of Health and Life Sciences, Newcastle upon Tyne, England, UK.
Microbial Environments, Hub for Biotechnology in the Built Environment, Newcastle upon Tyne, England, UK.
Arch Dis Child Fetal Neonatal Ed. 2023 May;108(3):272-279. doi: 10.1136/archdischild-2022-324477. Epub 2022 Nov 17.
To determine the impact of supplemental bovine lactoferrin on the gut microbiome and metabolome of preterm infants.
Cohort study nested within a randomised controlled trial (RCT). Infants across different trial arms were matched on several clinical variables. Bacteria and metabolite compositions of longitudinal stool and urine samples were analysed to investigate the impact of lactoferrin supplementation.
Thirteen UK hospitals participating in a RCT of lactoferrin.
479 infants born <32 weeks' gestation between June 2016 and September 2017.
10 990 stool and 22 341 urine samples were collected. Analyses of gut microbiome (1304 stools, 201 infants), metabolites (171 stools, 83 infants; 225 urines, 90 infants) and volatile organic compounds (314 stools, 117 infants) were performed. Gut microbiome Shannon diversity at 34 weeks corrected age was not significantly different between infants in the lactoferrin (mean=1.24) or placebo (mean=1.06) groups (p=0.11). Lactoferrin receipt explained less than 1% variance in microbiome compositions between groups. Metabolomic analysis identified six discriminative features between trial groups. Hospital site (16%) and postnatal age (6%) explained the greatest variation in microbiome composition.
This multiomic study identified minimal impacts of lactoferrin but much larger impacts of hospital site and postnatal age. This may be due to the specific lactoferrin product used, but more likely supports the findings of the RCT in which this study was nested, which showed no impact of lactoferrin on reducing rates of sepsis. Multisite mechanistic studies nested within RCTs are feasible and help inform trial interpretation and future trial design.
确定补充牛乳铁蛋白对早产儿肠道微生物组和代谢组的影响。
嵌套于随机对照试验(RCT)的队列研究。在不同试验组的婴儿在多个临床变量上进行匹配。对纵向粪便和尿液样本的细菌和代谢物组成进行分析,以研究乳铁蛋白补充的影响。
英国 13 家参与乳铁蛋白 RCT 的医院。
2016 年 6 月至 2017 年 9 月期间出生<32 周的 479 名婴儿。
共收集了 10990 份粪便和 22341 份尿液样本。对肠道微生物组(1304 份粪便,201 名婴儿)、代谢物(171 份粪便,83 名婴儿;225 份尿液,90 名婴儿)和挥发性有机化合物(314 份粪便,117 名婴儿)进行了分析。34 周校正年龄时,乳铁蛋白组(均值=1.24)和安慰剂组(均值=1.06)婴儿的肠道微生物组 Shannon 多样性无显著差异(p=0.11)。乳铁蛋白的摄入对组间微生物组组成的差异解释不到 1%。代谢组学分析确定了两组之间的六个有区别的特征。医院地点(16%)和出生后年龄(6%)解释了微生物组组成最大的变异。
这项多组学研究发现乳铁蛋白的影响很小,但医院地点和出生后年龄的影响很大。这可能是由于使用了特定的乳铁蛋白产品,但更可能支持这项研究嵌套的 RCT 的研究结果,该 RCT 表明乳铁蛋白对降低败血症发生率没有影响。嵌套于 RCT 的多地点机制研究是可行的,并有助于为试验解释和未来的试验设计提供信息。