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      Interpretable Machine Learning Framework Reveals Robust Gut Microbiome Features Associated With Type 2 Diabetes

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          Abstract

          OBJECTIVE

          To identify the core gut microbial features associated with type 2 diabetes risk and potential demographic, adiposity, and dietary factors associated with these features.

          RESEARCH DESIGN AND METHODS

          We used an interpretable machine learning framework to identify the type 2 diabetes–related gut microbiome features in the cross-sectional analyses of three Chinese cohorts: one discovery cohort ( n = 1,832, 270 cases of type 2 diabetes) and two validation cohorts (cohort 1: n = 203, 48 cases; cohort 2: n = 7,009, 608 cases). We constructed a microbiome risk score (MRS) with the identified features. We examined the prospective association of the MRS with glucose increment in 249 participants without type 2 diabetes and assessed the correlation between the MRS and host blood metabolites ( n = 1,016). We transferred human fecal samples with different MRS levels to germ-free mice to confirm the MRS–type 2 diabetes relationship. We then examined the prospective association of demographic, adiposity, and dietary factors with the MRS ( n = 1,832).

          RESULTS

          The MRS (including 14 microbial features) consistently associated with type 2 diabetes, with risk ratio for per 1-unit change in MRS 1.28 (95% CI 1.23–1.33), 1.23 (1.13–1.34), and 1.12 (1.06–1.18) across three cohorts. The MRS was positively associated with future glucose increment ( P < 0.05) and was correlated with a variety of gut microbiota–derived blood metabolites. Animal study further confirmed the MRS–type 2 diabetes relationship. Body fat distribution was found to be a key factor modulating the gut microbiome–type 2 diabetes relationship.

          CONCLUSIONS

          Our results reveal a core set of gut microbiome features associated with type 2 diabetes risk and future glucose increment.

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          Most cited references36

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          QIIME allows analysis of high-throughput community sequencing data.

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            pROC: an open-source package for R and S+ to analyze and compare ROC curves

            Background Receiver operating characteristic (ROC) curves are useful tools to evaluate classifiers in biomedical and bioinformatics applications. However, conclusions are often reached through inconsistent use or insufficient statistical analysis. To support researchers in their ROC curves analysis we developed pROC, a package for R and S+ that contains a set of tools displaying, analyzing, smoothing and comparing ROC curves in a user-friendly, object-oriented and flexible interface. Results With data previously imported into the R or S+ environment, the pROC package builds ROC curves and includes functions for computing confidence intervals, statistical tests for comparing total or partial area under the curve or the operating points of different classifiers, and methods for smoothing ROC curves. Intermediary and final results are visualised in user-friendly interfaces. A case study based on published clinical and biomarker data shows how to perform a typical ROC analysis with pROC. Conclusions pROC is a package for R and S+ specifically dedicated to ROC analysis. It proposes multiple statistical tests to compare ROC curves, and in particular partial areas under the curve, allowing proper ROC interpretation. pROC is available in two versions: in the R programming language or with a graphical user interface in the S+ statistical software. It is accessible at http://expasy.org/tools/pROC/ under the GNU General Public License. It is also distributed through the CRAN and CSAN public repositories, facilitating its installation.
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              Greengenes, a Chimera-Checked 16S rRNA Gene Database and Workbench Compatible with ARB

              A 16S rRNA gene database ( http://greengenes.lbl.gov ) addresses limitations of public repositories by providing chimera screening, standard alignment, and taxonomic classification using multiple published taxonomies. It was found that there is incongruent taxonomic nomenclature among curators even at the phylum level. Putative chimeras were identified in 3% of environmental sequences and in 0.2% of records derived from isolates. Environmental sequences were classified into 100 phylum-level lineages in the Archaea and Bacteria .
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                Author and article information

                Journal
                Diabetes Care
                Diabetes Care
                diacare
                dcare
                Diabetes Care
                Diabetes Care
                American Diabetes Association
                0149-5992
                1935-5548
                February 2021
                7 December 2020
                7 December 2020
                : 44
                : 2
                : 358-366
                Affiliations
                [1] 1Key Laboratory of Growth Regulation and Translational Research of Zhejiang Province, School of Life Sciences, Westlake University, Hangzhou, China
                [2] 2Guangdong Provincial Key Laboratory of Food, Nutrition and Health, Department of Epidemiology, School of Public Health, Sun Yat-sen University, Guangzhou, China
                [3] 3Microbiome Medicine Center, Division of Laboratory Medicine, Zhujiang Hospital, Southern Medical University, Guangzhou, China
                [4] 4Institute of Basic Medical Sciences, Westlake Institute for Advanced Study, Hangzhou, China
                [5] 5State Key Laboratory of Organ Failure Research, Southern Medical University, Guangzhou, China
                [6] 6Westlake Laboratory of Life Sciences and Biomedicine, Hangzhou, China
                Author notes
                Corresponding authors: Ju-Sheng Zheng, zhengjusheng@ 123456westlake.edu.cn , and Yu-ming Chen, chenyum@ 123456mail.sysu.edu.cn
                Author information
                https://orcid.org/0000-0003-1658-5528
                https://orcid.org/0000-0001-6560-4890
                Article
                201536
                10.2337/dc20-1536
                7818326
                33288652
                1854d7c9-33d2-434d-946b-4d96a3b50629
                © 2020 by the American Diabetes Association

                Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. More information is available at https://www.diabetesjournals.org/content/license.

                History
                : 22 June 2020
                : 23 October 2020
                Page count
                Figures: 2, Tables: 2, Equations: 0, References: 39, Pages: 9
                Funding
                Funded by: Zhejiang Province Ten-thousand Talents Program
                Award ID: 81903316
                Award ID: 81773416
                Award ID: 101396522001
                Funded by: 5010 Program for Clinical Research
                Award ID: 81903316
                Award ID: 81773416
                Award ID: 2007032
                Categories
                0406
                Epidemiology/Health Services Research

                Endocrinology & Diabetes
                Endocrinology & Diabetes

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