Literature DB >> 25957468

Testing in Microbiome-Profiling Studies with MiRKAT, the Microbiome Regression-Based Kernel Association Test.

Ni Zhao1, Jun Chen2, Ian M Carroll3, Tamar Ringel-Kulka4, Michael P Epstein5, Hua Zhou6, Jin J Zhou7, Yehuda Ringel3, Hongzhe Li8, Michael C Wu9.   

Abstract

High-throughput sequencing technology has enabled population-based studies of the role of the human microbiome in disease etiology and exposure response. Distance-based analysis is a popular strategy for evaluating the overall association between microbiome diversity and outcome, wherein the phylogenetic distance between individuals' microbiome profiles is computed and tested for association via permutation. Despite their practical popularity, distance-based approaches suffer from important challenges, especially in selecting the best distance and extending the methods to alternative outcomes, such as survival outcomes. We propose the microbiome regression-based kernel association test (MiRKAT), which directly regresses the outcome on the microbiome profiles via the semi-parametric kernel machine regression framework. MiRKAT allows for easy covariate adjustment and extension to alternative outcomes while non-parametrically modeling the microbiome through a kernel that incorporates phylogenetic distance. It uses a variance-component score statistic to test for the association with analytical p value calculation. The model also allows simultaneous examination of multiple distances, alleviating the problem of choosing the best distance. Our simulations demonstrated that MiRKAT provides correctly controlled type I error and adequate power in detecting overall association. "Optimal" MiRKAT, which considers multiple candidate distances, is robust in that it suffers from little power loss in comparison to when the best distance is used and can achieve tremendous power gain in comparison to when a poor distance is chosen. Finally, we applied MiRKAT to real microbiome datasets to show that microbial communities are associated with smoking and with fecal protease levels after confounders are controlled for.
Copyright © 2015 The American Society of Human Genetics. Published by Elsevier Inc. All rights reserved.

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Year:  2015        PMID: 25957468      PMCID: PMC4570290          DOI: 10.1016/j.ajhg.2015.04.003

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  27 in total

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  106 in total

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7.  The respiratory tract microbiome and its relationship to lung cancer and environmental exposures found in rural china.

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8.  Cigarette smoking and oral microbiota in low-income and African-American populations.

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9.  Phylogeny-corrected identification of microbial gene families relevant to human gut colonization.

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