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中重度早产儿肠道微生物组可逆性紊乱:一项随机对照试验的结果。

Reversible aberrancies in gut microbiome of moderate and late preterm infants: results from a randomized, controlled trial.

机构信息

Department of Pediatrics and Adolescent medicine, Turku University Hospital, Turku, Finland.

Institute of Clinical Medicine, University of Turku, Turku, Finland.

出版信息

Gut Microbes. 2023 Dec;15(2):2283913. doi: 10.1080/19490976.2023.2283913. Epub 2023 Nov 27.

Abstract

The aim of this study was to obtain insight into the composition and function of the deviant gut microbiome throughout infancy in children born moderately and late preterm and their response to microbiome modulation. We characterized the longitudinal development of the gut microbiome from birth to the age of 12 months by metagenomic sequencing in 43 moderate and late preterm children participating in a randomized, controlled trial (ClinicalTrials.gov/no.NCT00167700) assessing the impact of a probiotic ( GG, ATCC 53,103, currently ) and a prebiotic (galacto-oligosaccharide and polydextrose mixture, 1:1) intervention as compared to a placebo administered from 3 to 60 days of life. In addition, 9 full-term, vaginally delivered, breast-fed infants, who remained healthy long-term were included as references. Significant differences in taxonomy, but not in functional potential, were found when comparing the gut microbiome composition of preterm and full-term infants during the first month of life. However, the gut microbiome of preterm infants resembled that of full-term infants by 6 months age. Probiotic and prebiotic treatments were found to mitigate the shift in the microbiome of preterm infants by accelerating -dominated gut microbiome in beta diversity analysis. This study provides intriguing information regarding the establishment of the gut microbiome in children born moderately and late preterm, representing the majority of children born preterm. Specific pro- and prebiotics may reverse the proinflammatory gut microbiome composition during the vulnerable period, when the microbiome is low in resilience and susceptible to environmental exposure and simultaneously promotes immunological and metabolic maturation.

摘要

本研究旨在深入了解中晚期早产儿婴儿在整个婴儿期肠道微生物组的组成和功能,以及其对微生物组调节的反应。我们通过对 43 名参与随机对照试验(ClinicalTrials.gov/no.NCT00167700)的中晚期早产儿进行宏基因组测序,描述了肠道微生物组从出生到 12 个月的纵向发育情况,该试验评估了益生菌( GG ,ATCC 53,103 ,目前)和益生元(半乳糖 - 低聚糖和聚右旋糖混合物,1:1)干预对肠道微生物组的影响与生命 3 至 60 天内给予安慰剂相比。此外,还纳入了 9 名足月、阴道分娩、母乳喂养的婴儿作为参考,这些婴儿长期保持健康。在生命的第一个月,当比较早产儿和足月儿的肠道微生物组组成时,发现了分类学上的显著差异,但功能潜力没有差异。然而,到 6 个月时,早产儿的肠道微生物组与足月儿的肠道微生物组相似。益生菌和益生元治疗被发现通过加速β多样性分析中占主导地位的微生物组来减轻早产儿肠道微生物组的转移。这项研究提供了关于中晚期早产儿出生的儿童肠道微生物组建立的有趣信息,这些儿童占早产儿的大多数。特定的益生菌和益生元可能会在肠道微生物组易受环境暴露影响且同时促进免疫和代谢成熟的脆弱时期逆转促炎肠道微生物组组成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2bd/10730193/7f2b7e224e8c/KGMI_A_2283913_F0001_OC.jpg

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