06: Bayesian Sparse Regression for the Association of Microbiome Profiles with Metabolite Abundance

Christine Peterson Co-Author
University of Texas MD Anderson Cancer Center
 
Kai Jiang First Author
The University of Texas Health Science Center as Houston
 
Kai Jiang Presenting Author
The University of Texas Health Science Center as Houston
 
Monday, Aug 4: 10:30 AM - 12:20 PM
1680 
Contributed Posters 
Music City Center 
Numerous studies have shown that microbial metabolites, which represent the products of bacteria in the human gut, play a key role in shaping cancer risk and response to treatment. However, metabolite data typically contain a large proportion of missing values which are often recorded as zeros. These missing values may result from either low abundance or technical challenges in data processing. Moreover, given the compositionality of microbiome data, where the observed abundances can only be interpreted on a relative scale, standard variable selection methods are not applicable. In this project, we propose a novel Bayesian method to address challenges in both metabolite and microbiome data. Key features of our proposed model include adopting a z-prior to address the compositional characteristics of microbiome data and modeling the two different mechanisms of missing metabolite data. We demonstrate on simulated data that our proposed model can impute the unobserved true metabolite values and correctly select the relevant microbiome predictors. We illustrate our method on real data from a study on the interplay between the microbiome and metabolome in colorectal cancer.

Keywords

Bayesian variable selection

Compositional covariates

Metabolome outcome

Microbiome data analysis

Missing value imputation 

Abstracts


Main Sponsor

Biometrics Section