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      Bacterial Taxa and Functions Are Predictive of Sustained Remission Following Exclusive Enteral Nutrition in Pediatric Crohn’s Disease

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          Abstract

          Background

          The gut microbiome is extensively involved in induction of remission in pediatric Crohn’s disease (CD) patients by exclusive enteral nutrition (EEN). In this follow-up study of pediatric CD patients undergoing treatment with EEN, we employ machine learning models trained on baseline gut microbiome data to distinguish patients who achieved and sustained remission (SR) from those who did not achieve remission nor relapse (non-SR) by 24 weeks.

          Methods

          A total of 139 fecal samples were obtained from 22 patients (8–15 years of age) for up to 96 weeks. Gut microbiome taxonomy was assessed by 16S rRNA gene sequencing, and functional capacity was assessed by metagenomic sequencing. We used standard metrics of diversity and taxonomy to quantify differences between SR and non-SR patients and to associate gut microbial shifts with fecal calprotectin (FCP), and disease severity as defined by weighted Pediatric Crohn’s Disease Activity Index. We used microbial data sets in addition to clinical metadata in random forests (RFs) models to classify treatment response and predict FCP levels.

          Results

          Microbial diversity did not change after EEN, but species richness was lower in low-FCP samples (<250 µg/g). An RF model using microbial abundances, species richness, and Paris disease classification was the best at classifying treatment response (area under the curve [AUC] = 0.9). KEGG Pathways also significantly classified treatment response with the addition of the same clinical data (AUC = 0.8). Top features of the RF model are consistent with previously identified IBD taxa, such as Ruminococcaceae and Ruminococcus gnavus.

          Conclusions

          Our machine learning approach is able to distinguish SR and non-SR samples using baseline microbiome and clinical data.

          Abstract

          Here, authors present a follow-up on a cohort of 22 pediatric CD patients undergoing EEN treatment to induce remission. They leverage machine learning techniques to show that the baseline microbiome with clinical metadata can predict sustained remission.

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          Most cited references25

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          Roles for Intestinal Bacteria, Viruses, and Fungi in Pathogenesis of Inflammatory Bowel Diseases and Therapeutic Approaches.

          Intestinal microbiota are involved in the pathogenesis of Crohn's disease, ulcerative colitis, and pouchitis. We review the mechanisms by which these gut bacteria, fungi, and viruses mediate mucosal homeostasis via their composite genes (metagenome) and metabolic products (metabolome). We explain how alterations to their profiles and functions under conditions of dysbiosis contribute to inflammation and effector immune responses that mediate inflammatory bowel diseases (IBD) in humans and enterocolitis in mice. It could be possible to engineer the intestinal environment by modifying the microbiota community structure or function to treat patients with IBD-either with individual agents, via dietary management, or as adjuncts to immunosuppressive drugs. We summarize the latest information on therapeutic use of fecal microbial transplantation and propose improved strategies to selectively normalize the dysbiotic microbiome in personalized approaches to treatment.
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            Mechanisms of Disease: Inflammatory Bowel Diseases

            Inflammatory bowel diseases (IBDs), represented by Crohn disease and ulcerative colitis, are associated with major morbidity in Western countries and with increasing incidence in the developing world. Although analysis of the genome of patients with IBD, especially through genome-wide association studies, has unraveled multiple pathways involved in IBD pathogenesis, only part of IBD heritability has been explained by genetic studies. This finding has revealed that environmental factors also play a major role in promoting intestinal inflammation, mostly through their effects in the composition of the microbiome. However, in order for microbial dysbiosis to result in uncontrolled intestinal inflammation, the intestinal barrier formed by intestinal epithelial cells and the innate immune system should also be compromised. Finally, activation of the immune system depends on the working balance between effector and regulatory cells present in the intestinal mucosa, which have also been found to be dysregulated in this patient population. Therefore, IBD pathogenesis is a result of the interplay of genetic susceptibility and environmental impact on the microbiome that through a weakened intestinal barrier will lead to inappropriate intestinal immune activation. In this article, we will review the mechanisms proposed to cause IBD from the genetic, environmental, intestinal barrier, and immunologic perspectives.
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              GLUMIP 2.0: SAS/IML Software for Planning Internal Pilots.

              Internal pilot designs involve conducting interim power analysis (without interim data analysis) to modify the final sample size. Recently developed techniques have been described to avoid the type I error rate inflation inherent to unadjusted hypothesis tests, while still providing the advantages of an internal pilot design. We present GLUMIP 2.0, the latest version of our free SAS/IML software for planning internal pilot studies in the general linear univariate model (GLUM) framework. The new analytic forms incorporated into the updated software solve many problems inherent to current internal pilot techniques for linear models with Gaussian errors. Hence, the GLUMIP 2.0 software makes it easy to perform exact power analysis for internal pilots under the GLUM framework with independent Gaussian errors and fixed predictors.
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                Author and article information

                Journal
                Inflamm Bowel Dis
                Inflamm. Bowel Dis
                ibd
                Inflammatory Bowel Diseases
                Oxford University Press (US )
                1078-0998
                1536-4844
                July 2020
                21 January 2020
                21 January 2020
                : 26
                : 7
                : 1026-1037
                Affiliations
                [1 ] Department of Pharmacology, Dalhousie University , Halifax, Canada
                [2 ] Department of Pediatrics, Dalhousie University , Halifax, Canada
                [3 ] Department of Biology, Dalhousie University , Halifax, Canada
                [4 ] Department of Mathematics & Statistics, Dalhousie University , Halifax, Canada
                [5 ] Integrated Microbiome Resource (IMR), Dalhousie University , Halifax, Canada
                [6 ] Tytgat Institute for Liver and Intestinal Research, Amsterdam Gastroenterology and Metabolism, Academic Medical Center, University of Amsterdam , Amsterdam, the Netherlands
                [7 ] Department of Pediatrics, Division of Pediatric Gastroenterology & Nutrition, Emma Children’s Hospital, Academic Medical Center, University of Amsterdam , Amsterdam, the Netherlands
                Author notes
                Address correspondence to: Johan Van Limbergen MD, FRCPCH, PhD, Afdeling Kindergeneeskunde/Maag-, Darm- en Leverziekten, Locatie AMC, H7-228, Meibergdreef 9, 1105 AZ Amsterdam, the Netherlands. E-mail: j.e.vanlimbergen@ 123456amsterdamumc.nl .
                Article
                izaa001
                10.1093/ibd/izaa001
                7301407
                31961432
                5059890f-9d6e-41d3-80e7-7f514074167e
                © 2020 Crohn’s & Colitis Foundation. Published by Oxford University Press on behalf of Crohn’s & Colitis Foundation.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License ( http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

                History
                : 29 July 2019
                : 16 December 2019
                Page count
                Pages: 12
                Funding
                Funded by: Canadian Institutes of Health Research, DOI 10.13039/501100000024;
                Funded by: Canadian Association of Gastroenterology, DOI 10.13039/501100000149;
                Funded by: Crohn's and Colitis Canada, DOI 10.13039/501100007658;
                Funded by: Canadian Foundation of Innovation John R. Evans Leadership;
                Award ID: 35235
                Award ID: 36764
                Funded by: Nova Scotia Health Research Foundation, DOI 10.13039/501100000194;
                Categories
                Basic Science Research
                AcademicSubjects/MED00260

                Gastroenterology & Hepatology
                pediatric crohn’s disease,exclusive enteral nutrition,gut microbiome,nutrition in pediatrics

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