Literature DB >> 31702998

A Bayesian framework for identifying consistent patterns of microbial abundance between body sites.

Richard Meier1, Jeffrey A Thompson1, Mei Chung2, Naisi Zhao2, Karl T Kelsey3, Dominique S Michaud2, Devin C Koestler1.   

Abstract

Recent studies have found that the microbiome in both gut and mouth are associated with diseases of the gut, including cancer. If resident microbes could be found to exhibit consistent patternpan>s between the mouth anpan>d gut, disease status could potentially be assessed non-invasively through profiling of oral samples. Currently, there exists no generally applicable method to test for such associations. Here we present a Bayesianpan> framework to identify microbes that exhibit consistent patternpan>s between body sites, with respect to a phenotypic variable. For a given operational taxonomic unit (OTU), a Bayesianpan> regression model is used to obtain Markov-Chain Monte Carlo estimates of abundanpan>ce among strata, calculate a correlation statistic, anpan>d conduct a formal test based on its posterior distribution. Extensive simulation studies demonstrate overall viability of the approach, anpan>d provide information on what factors affect its performanpan>ce. Applying our method to a dataset containing oral anpan>d pan> class="Species">gut microbiome samples from 77 pancreatic cancer patients revealed several OTUs exhibiting consistent patterns between gut and mouth with respect to disease subtype. Our method is well powered for modest sample sizes and moderate strength of association and can be flexibly extended to other research settings using any currently established Bayesian analysis programs.

Entities:  

Keywords:  Bayesian; association; consistent pattern; microbial abundance; microbiome; zero-inflated beta regression

Mesh:

Year:  2019        PMID: 31702998      PMCID: PMC7944583          DOI: 10.1515/sagmb-2019-0027

Source DB:  PubMed          Journal:  Stat Appl Genet Mol Biol        ISSN: 1544-6115


  18 in total

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8.  Plasma antibodies to oral bacteria and risk of pancreatic cancer in a large European prospective cohort study.

Authors:  Dominique S Michaud; Jacques Izard; Charlotte S Wilhelm-Benartzi; Doo-Ho You; Verena A Grote; Anne Tjønneland; Christina C Dahm; Kim Overvad; Mazda Jenab; Veronika Fedirko; Marie Christine Boutron-Ruault; Françoise Clavel-Chapelon; Antoine Racine; Rudolf Kaaks; Heiner Boeing; Jana Foerster; Antonia Trichopoulou; Pagona Lagiou; Dimitrios Trichopoulos; Carlotta Sacerdote; Sabina Sieri; Domenico Palli; Rosario Tumino; Salvatore Panico; Peter D Siersema; Petra H M Peeters; Eiliv Lund; Aurelio Barricarte; José-María Huerta; Esther Molina-Montes; Miren Dorronsoro; J Ramón Quirós; Eric J Duell; Weimin Ye; Malin Sund; Björn Lindkvist; Dorthe Johansen; Kay-Tee Khaw; Nick Wareham; Ruth C Travis; Paolo Vineis; H Bas Bueno-de-Mesquita; Elio Riboli
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10.  A marginalized two-part Beta regression model for microbiome compositional data.

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Journal:  PLoS Comput Biol       Date:  2018-07-23       Impact factor: 4.475

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  1 in total

1.  Comparisons of oral, intestinal, and pancreatic bacterial microbiomes in patients with pancreatic cancer and other gastrointestinal diseases.

Authors:  Mei Chung; Naisi Zhao; Richard Meier; Devin C Koestler; Guojun Wu; Erika de Castillo; Bruce J Paster; Kevin Charpentier; Jacques Izard; Karl T Kelsey; Dominique S Michaud
Journal:  J Oral Microbiol       Date:  2021-02-14       Impact factor: 5.474

  1 in total

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