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以牛奶来源的低聚糖为基础的配方奶粉可使足月婴儿的肠道微生物群更接近母乳喂养婴儿的肠道微生物群,并改善肠道免疫防御:一项随机对照试验。

Term infant formula supplemented with milk-derived oligosaccharides shifts the gut microbiota closer to that of human milk-fed infants and improves intestinal immune defense: a randomized controlled trial.

机构信息

Asian Hospital and Medical Center, Muntinlupa City, Philippines.

Nestlé Institute of Health Sciences, Nestlé Research, Lausanne, Switzerland.

出版信息

Am J Clin Nutr. 2022 Jan 11;115(1):142-153. doi: 10.1093/ajcn/nqab336.

DOI:10.1093/ajcn/nqab336
PMID:34617558
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8755036/
Abstract

BACKGROUND

Bovine milk-derived oligosaccharides (MOS) containing primarily galacto-oligosaccharides with inherent concentrations of sialylated oligosaccharides can be added to infant formula to enhance the oligosaccharide profile.

OBJECTIVE

To investigate the effects of an MOS-supplemented infant formula on gut microbiota and intestinal immunity.

METHODS

In a double-blind, randomized, controlled trial, healthy term formula-fed infants aged 21-26 d either received an intact protein cow milk-based formula (control group, CG, n = 112) or the same formula containing 7.2 g MOS/L (experimental group, EG, n = 114) until the age of 6 mo. Exclusively human milk-fed infants (HFI, n = 70) from an observational study served as the reference. Fecal samples collected at baseline, and the ages of 2.5 and 4 mo were assessed for microbiota (16S ribosomal RNA-based approaches), metabolites, and biomarkers of gut health and immune response.

RESULTS

Aged 2.5 and 4 mo, redundancy analysis (P = 0.002) and average phylogenetic distance (P < 0.05) showed that the overall microbiota composition in EG was different from CG and closer to that of HFI. Similarly, EG caesarean-born infants were different from CG caesarean- or vaginally born infants and approaching HFI vaginally born infants. Relative bifidobacteria abundance was higher in EG compared with CG (P < 0.05) approaching HFI. At the age of 4 mo, counts of Clostridioides difficile and Clostridium perfringens were ∼90% (P < 0.001) and ∼65% (P < 0.01) lower in EG compared with CG, respectively. Geometric LS mean (95% CI) fecal secretory IgA in EG was twice that of CG [70 (57, 85) compared with 34 (28, 42) mg/g, P < 0.001] and closer to HFI. Fecal oral polio vaccine-specific IgA was ∼50% higher in EG compared with CG (P = 0.065). Compared with CG, EG and HFI had lower fecal calcium excretion (by ∼30%, P < 0.005) and fecal pH (P < 0.001), and higher lactate concentration (P < 0.001).

CONCLUSIONS

Infant formula with MOS shifts the gut microbiota and metabolic signature closer to that of HFI, has a strong bifidogenic effect, reduces fecal pathogens, and improves the intestinal immune response.

摘要

背景

牛源低聚糖(MOS)主要含有半乳糖低聚糖,具有固有浓度的唾液酸化低聚糖,可以添加到婴儿配方奶粉中,以增强低聚糖谱。

目的

研究添加 MOS 的婴儿配方奶粉对肠道微生物群和肠道免疫的影响。

方法

在一项双盲、随机、对照试验中,年龄在 21-26 天的健康足月配方奶喂养婴儿分别接受完整蛋白牛乳基配方(对照组,CG,n=112)或含有 7.2g MOS/L 的相同配方(实验组,EG,n=114),直至 6 月龄。来自观察性研究的纯人乳喂养婴儿(HFI,n=70)作为参考。在基线时、2.5 月龄和 4 月龄采集粪便样本,用于评估肠道健康和免疫反应的微生物群(16S 核糖体 RNA 方法)、代谢物和生物标志物。

结果

2.5 月龄和 4 月龄时,冗余分析(P=0.002)和平均系统发育距离(P<0.05)表明,EG 的整体微生物群组成与 CG 不同,与 HFI 更接近。同样,EG 剖宫产出生的婴儿与 CG 剖宫产或阴道出生的婴儿不同,与 HFI 阴道出生的婴儿接近。与 CG 相比,EG 中的双歧杆菌相对丰度更高(P<0.05),接近 HFI。4 月龄时,与 CG 相比,艰难梭菌和产气荚膜梭菌的计数分别降低了约 90%(P<0.001)和 65%(P<0.01)。EG 的粪便分泌型 IgA 的几何 LS 均值(95%CI)是 CG 的两倍[70(57,85)比 34(28,42)mg/g,P<0.001],与 HFI 更接近。与 CG 相比,EG 中的口服脊髓灰质炎疫苗特异性 IgA 高约 50%(P=0.065)。与 CG 相比,EG 和 HFI 的粪便钙排泄量减少约 30%(P<0.005),粪便 pH 值降低(P<0.001),乳酸浓度升高(P<0.001)。

结论

添加 MOS 的婴儿配方奶粉使肠道微生物群和代谢特征更接近 HFI,具有强烈的双歧杆菌作用,减少粪便病原体,改善肠道免疫反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92ba/8755036/9ebfe92a4095/nqab336fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92ba/8755036/b4ea57d29b0f/nqab336fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92ba/8755036/a05b988451bc/nqab336fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92ba/8755036/94af7dced5dc/nqab336fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92ba/8755036/cbec735d386e/nqab336fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92ba/8755036/8167a1960098/nqab336fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92ba/8755036/9ebfe92a4095/nqab336fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92ba/8755036/b4ea57d29b0f/nqab336fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92ba/8755036/a05b988451bc/nqab336fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92ba/8755036/94af7dced5dc/nqab336fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92ba/8755036/cbec735d386e/nqab336fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92ba/8755036/8167a1960098/nqab336fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92ba/8755036/9ebfe92a4095/nqab336fig6.jpg

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