Testing microbiome associations with survival times at both the community and individual taxon levels

• Type of Material: Article
• Authors: Yingtian Hu, Emory University; Yunxiao Li, Emory University; Glen Satten, Emory University; Yijuan Hu, Emory University
• Language: English
• Date: 2022-09-01
• Publisher: Emory University Libraries
• Publication Version: Author Accepted Manuscript (After Peer Review)
• Copyright Statement: © 2022 Hu et al
• Final Published Version (URL): http://dx.doi.org/10.1371/journal.pcbi.1010509
• Title of Journal or Parent Work: PLoS Computational Biology
• Volume: 18
• Issue: 9
• Start Page: e1010509
• End Page: e1010509
• Grant/Funding Information: This research was supported by the National Institutes of Health awards R01GM116065 (YJH, GAS) and R01GM141074 (YJH, GAS). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
• Keywords: Sample Size; Proportional Hazards Models; Microbiota; Linear Models; Gastrointestinal Microbiome
• Research Categories: Biology, Biostatistics; Health Sciences, Obstetrics and Gynecology

Abstract

Finding microbiome associations with possibly censored survival times is an important problem, especially as specific taxa could serve as biomarkers for disease prognosis or as targets for therapeutic interventions. The two existing methods for survival outcomes, MiRKAT-S and OMiSA, are restricted to testing associations at the community level and do not provide results at the individual taxon level. An ad hoc approach testing each taxon with a survival outcome using the Cox proportional hazard model may not perform well in the microbiome setting with sparse count data and small sample sizes. Methods We have previously developed the linear decomposition model (LDM) for testing continuous or discrete outcomes that unifies community-level and taxon-level tests into one framework. Here we extend the LDM to test survival outcomes. We propose to use the Martingale residuals or the deviance residuals obtained from the Cox model as continuous covariates in the LDM. We further construct tests that combine the results of analyzing each set of residuals separately. Finally, we extend PERMANOVA, the most commonly used distance-based method for testing community-level hypotheses, to handle survival outcomes in a similar manner. Results Using simulated data, we showed that the LDM-based tests preserved the false discovery rate for testing individual taxa and had good sensitivity. The LDM-based community-level tests and PERMANOVA-based tests had comparable or better power than MiRKAT-S and OMiSA. An analysis of data on the association of the gut microbiome and the time to acute graft-versus-host disease revealed several dozen associated taxa that would not have been achievable by any community-level test, as well as improved community-level tests by the LDM and PERMANOVA over those obtained using MiRKAT-S and OMiSA. Conclusions Unlike existing methods, our new methods are capable of discovering individual taxa that are associated with survival times, which could be of important use in clinical settings.