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      Supplementation with Akkermansia muciniphila in overweight and obese human volunteers: a proof-of-concept exploratory study

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          Abstract

          Metabolic syndrome is characterized by a constellation of comorbidities that predispose individuals to an increased risk of developing cardiovascular pathologies as well as type 2 diabetes mellitus (T2DM) 1 . The gut microbiota is considered as a new key contributor involved in the onset of obesity-related disorders 2 . In humans, studies have provided evidence for a negative correlation between Akkermansia muciniphila abundance and overweight, obesity, untreated T2DM, or hypertension 38 . As the administration of A.muciniphila has never been investigated in humans, we conducted a randomized double-blind placebo-controlled pilot study in overweight/obese insulin resistant volunteers, 40 were enroled and 32 completed the trial. The primary endpoints were on safety, tolerability and metabolic parameters (i.e., insulin resistance, circulating lipids, visceral adiposity, body mass). The secondary outcomes were the gut barrier function (i.e., plasma lipopolysacharrides (LPS) and gut microbiota composition. In this single-center study, we demonstrated that daily oral supplementation of 10 10 bacteria either alive or pasteurized A.muciniphila for 3 months was safe and well tolerated. Compared to the Placebo, pasteurized A.muciniphila improved insulin sensitivity (+28.62±7.02%, P=0.002), reduced insulinemia (-34.08±7.12%, P=0.006) and plasma total cholesterol (-8.68±2.38%, P=0.02). Pasteurized A.muciniphila supplementation slightly decreased body weight (-2.27±0.92kg, P=0.091) as compared to the Placebo group, and fat mass (-1.37±0.82kg, P=0.092) and hip circumference (-2.63±1.14cm, P = 0.091) as compared to baseline. After 3 months of supplementation, A.muciniphila reduced the levels of relevant blood markers of liver dysfunction and inflammation while the overall gut microbiome structure was unaffected. In conclusion, this proof-of-concept study (NCT02637115) shows that the intervention was safe and well-tolerated and that the supplementation with A.muciniphila improves several metabolic paramaters.

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          Recovery of ethanol-induced Akkermansia muciniphila depletion ameliorates alcoholic liver disease.

          Alcoholic liver disease (ALD) is a global health problem with limited therapeutic options. Intestinal barrier integrity and the microbiota modulate susceptibility to ALD. Akkermansia muciniphila, a Gram-negative intestinal commensal, promotes barrier function partly by enhancing mucus production. The aim of this study was to investigate microbial alterations in ALD and to define the impact of A. muciniphila administration on the course of ALD.
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            Compositional analysis: a valid approach to analyze microbiome high-throughput sequencing data.

            A workshop held at the 2015 annual meeting of the Canadian Society of Microbiologists highlighted compositional data analysis methods and the importance of exploratory data analysis for the analysis of microbiome data sets generated by high-throughput DNA sequencing. A summary of the content of that workshop, a review of new methods of analysis, and information on the importance of careful analyses are presented herein. The workshop focussed on explaining the rationale behind the use of compositional data analysis, and a demonstration of these methods for the examination of 2 microbiome data sets. A clear understanding of bioinformatics methodologies and the type of data being analyzed is essential, given the growing number of studies uncovering the critical role of the microbiome in health and disease and the need to understand alterations to its composition and function following intervention with fecal transplant, probiotics, diet, and pharmaceutical agents.
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              Akkermansia muciniphilainduces gut microbiota remodelling and controls islet autoimmunity in NOD mice

              Intestinal microbiota is implicated in the pathogenesis of autoimmune type 1 diabetes in humans and in non-obese diabetic (NOD) mice, but evidence on its causality and on the role of individual microbiota members is limited. We investigated if different diabetes incidence in two NOD colonies was due to microbiota differences and aimed to identify individual microbiota members with potential significance.
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                Author and article information

                Journal
                9502015
                Nat Med
                Nat. Med.
                Nature medicine
                1078-8956
                1546-170X
                01 July 2019
                01 July 2019
                05 June 2019
                01 January 2020
                : 25
                : 7
                : 1096-1103
                Affiliations
                [1 ]Metabolism and Nutrition Research Group, Louvain Drug Research Institute, Walloon Excellence in Life Sciences and BIOtechnology (WELBIO), UCLouvain, Université catholique de Louvain, Brussels, Belgium
                [2 ]Laboratory of Molecular Bacteriology- Department of Microbiology and Immunology, KU Leuven, Leuven, Belgium
                [3 ]Center for Microbiology, VIB, Leuven, Belgium
                [4 ]Pôle EDIN, Institut de Recherches Expérimentales et Cliniques IREC, UCLouvain, Université Catholique de Louvain, Belgium
                [5 ]Division of Endocrinology and Nutrition, Cliniques Universitaires St-Luc, Brussels, Belgium
                [6 ]Metabolism and Nutrition Research Group, Louvain Drug Research Institute, UCLouvain, Université catholique de Louvain, Brussels, Belgium
                [7 ]Laboratory of Microbiology, Wageningen University, Wageningen, the Netherlands
                [8 ]Human Microbiome Research Program, Faculty of Medicine, University of Helsinki, Helsinki, Finland
                Author notes
                [# ]Correspondence to: Patrice.cani@ 123456uclouvain.be , Prof. Patrice D. Cani, UCLouvain, Université catholique de Louvain, LDRI, Metabolism and Nutrition research group, Av. E. Mounier, 73 box B1.73.11, B-1200 Brussels, Belgium. Phone: +32 2 764 73 97
                [*]

                These first authors contributed equally to this work

                [9]

                These senior authors contributed equally

                Article
                EMS83212
                10.1038/s41591-019-0495-2
                6699990
                31263284
                503d0504-fab0-4932-a5d0-107df38f9933

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