ArticleFrontiers in microbiology2025
Effects of galactooligosaccharides on maternal metabolism and the gut microbiota during pregnancy.
Article in Frontiers in microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
1 citing paper in PubMed.
- The bidirectional gut microbiota-inflammation axis in gestational diabetes mellitus: pathogenesis, long-term outcomes, and therapeutic perspectives.Frontiers in endocrinology · 2026Review
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5 authors.
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Abstract
Background: The gut microbiota of pregnant women changes dynamically throughout gestation, adapting to the physiological changes of pregnancy. At the same time, dysbacteriosis is involved in the pathophysiological processes of pregnancy-related diseases. Research on gut microbiota and gestational diabetes mellitus (GDM) is relatively extensive, and targeting the gut microbiota may improve maternal health. Dietary supplements such as prebiotics improve metabolic immune function in pregnant women by stimulating the growth of beneficial bacteria and promoting the production of short-chain fatty acids (SCFAs). Previous animal studies suggest that prebiotic preparations derived from galactooligosaccharides (GOS) in human milk are superior to other prebiotics. Objective: This study aims to explore the systemic effects of GOS targeting the gut microbiota on the levels of metabolism, immunity, and circulating SCFAs. Materials and methods: (1) A total of 135 pregnant women with available delivery outcomes and matched BMI were included in the analysis. From the first trimester (T1), the GOS group and the control group received GOS and fructooligosaccharide (FOS) preparations, respectively. Before the intervention (T1) and after the intervention (T2), blood samples were collected from pregnant women for LC-MS metabolomic analysis and targeted detection of short-chain fatty acids. At the same time, clinical information, metabolic indicators, and the GDM incidence rate were compared between groups, and subgroup analyses were conducted for overweight and obese participants. Statistical analyses included the t-test, the nonparametric Wilcoxon test, and the Results: (1) Non-target metabolites identified several metabolites with inter-group differences: cyclamate, reserpic acid, and phenylbenzimidazole sulfonic acid were relatively higher in the GOS group. Pathway analysis indicated enrichment in butyrate, propionate, and other SCFA-related metabolic pathways, as well as in cysteine and methionine metabolism. (2) The targeted metabolites of SCFAs were further analyzed, and the effects of the intervention on SCFAs were compared. After GOS intervention, the levels of acetic acid, propionic acid, butyric acid, and hexanoic acid all increased ( Conclusion: GOS preparations containing ingredients derived from human milk may target the gut microbiota to promote the production of hexanoic acid, thereby improving lipid metabolism and inflammation, and may be beneficial for overweight and obese people with GDM.
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