Evidence map›Paper›PMID 30792016›Full record

ArticleMolecular metabolism2019

Synbiotic-driven improvement of metabolic disturbances is associated with changes in the gut microbiome in diet-induced obese mice.

Xinxin Ke, Alesia Walker, Sven-Bastiaan Haange, Ilias Lagkouvardos, Yuwen Liu, Philippe Schmitt-Kopplin, Martin von Bergen, Nico Jehmlich, Xin He, Thomas Clavel and 1 more

Open access · goldAbstract read
In one paragraph

Article in Molecular metabolism, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed, 2 pooled it
6.7field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

77 citing papers in PubMed, 2 syntheses or guidelines pooled it, 155 citations in OpenAlex.

  1. New Mediators in the Crosstalk between Different Adipose Tissues.International journal of molecular sciences · 2024
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  17. Synbiotic Administration of d-Tagatose andFood science & nutrition · 2025
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17 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 5 institutions in 4 countries.

Xinxin KeSchool of Life Sciences, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong, China.
Alesia WalkerResearch Unit Analytical BioGeoChemistry, HelmholtzZentrum München, Neuherberg, Germany.
Sven-Bastiaan HaangeHelmholtz-Centre for Environmental Research-UFZ, Department of Molecular Systems Biology, Leipzig, Germany.
Ilias LagkouvardosZIEL Institute for Food and Health, Technical University of Munich, Freising, Germany.
Yuwen LiuDepartment of Human Genetics, The University of Chicago, Chicago, IL, 60615, USA; Department of Pig Genomic Design and Breeding, Agricultural Genome Institute at Shenzhen, Chinese Academy of Agricultural Sciences, Shenzhen 518124, China.
Philippe Schmitt-KopplinResearch Unit Analytical BioGeoChemistry, HelmholtzZentrum München, Neuherberg, Germany; ZIEL Institute for Food and Health, Technical University of Munich, Freising, Germany; Chair of Analytical Food Chemistry, Technische Universität München, Freising-Weihenstephan, Germany.
Martin von BergenHelmholtz-Centre for Environmental Research-UFZ, Department of Molecular Systems Biology, Leipzig, Germany.
Nico JehmlichHelmholtz-Centre for Environmental Research-UFZ, Department of Molecular Systems Biology, Leipzig, Germany.
Xin HeDepartment of Human Genetics, The University of Chicago, Chicago, IL, 60615, USA.
Thomas ClavelZIEL Institute for Food and Health, Technical University of Munich, Freising, Germany; University Hospital of RWTH Aachen, Functional Microbiome Research Group, Institute of Medical Microbiology, Aachen, Germany.
Peter C K CheungSchool of Life Sciences, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong, China. Electronic address: petercheung@cuhk.edu.hk.
Helmholtz Centre for Environmental Research · DEChinese University of Hong Kong · HKHelmholtz Zentrum München · DELeibniz-Institute for Food Systems Biology at the Technical University of Munich · DEUniversity of Chicago · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe gut microbiota is an important influencing factor of metabolic health. Although dietary interventions with probiotics, prebiotics, and synbiotics can be effective means to regulate obesity and associated comorbidities, the underlying shifts in gut microbial communities, especially at the functional level, have not been characterized in great details. In this study, we sought to investigate the effects of synbiotics on the regulation of gut microbiota and the alleviation of high-fat diet (HFD)-induced metabolic disorders in mice.

methodsSpecific pathogen-free (SPF) male C57BL/6J mice were fed diets with either 10% (normal diet, ND) or 60% (high-fat diet, HFD) of total calories from fat (lard). Dietary interventions in the HFD-fed mice included (i) probiotic (Bifidobacterium animalis subsp. lactis and Lactobacillus paracasei subsp. paracasei DSM 46331), (ii) prebiotic (oat β-glucan), and (iii) synbiotic (a mixture of i and ii) treatments for 12 weeks. Besides detailed characterization of host metabolic parameters, a multi-omics approach was used to systematically profile the microbial signatures at both the phylogenetic and functional levels using 16S rRNA gene sequencing, metaproteomics and targeted metabolomics analysis.

resultsThe synbiotic intervention significantly reduced body weight gain and alleviated features of metabolic complications. At the phylogenetic level, the synbiotic treatment significantly reversed HFD-induced changes in microbial populations, both in terms of richness and the relative abundance of specific taxa. Potentially important species such as Faecalibaculum rodentium and Alistipes putredinis that might mediate the beneficial effects of the synbiotic were identified. At the functional level, short-chain fatty acid and bile acid profiles revealed that all dietary interventions significantly restored cecal levels of acetate, propionate, and butyrate, while the synbiotic treatment reduced the bile acid pools most efficiently. Metaproteomics revealed that the effects of the synbiotic intervention might be mediated through metabolic pathways involved in carbohydrate, amino acid, and energy metabolisms.

conclusionsOur results suggested that dietary intervention using the novel synbiotic can alleviate HFD-induced weight gain and restore gut microbial ecosystem homeostasis phylogenetically and functionally.

Indexed as

Gastrointestinal MicrobiomeSynbioticsAnimalsDiet, High-FatMaleMiceMice, Inbred C57BLMice, ObeseObesityDietary interventionGut microbiotaHigh-fat dietObesitySynbiotics

Identifiers

PMID30792016
PMCPMC6437638
OpenAlexW2914150653

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.