Bayesian Sparse Mediation Analysis with Targeted Penalization of Natural Indirect Effects.
Yanyi Song, Xiang Zhou, Jian Kang, Max T Aung, Min Zhang, Wei Zhao, Belinda L Needham, Sharon L R Kardia, Yongmei Liu, John D Meeker, Jennifer A Smith, Bhramar Mukherjee
Author Information
Yanyi Song: University of Michigan, Ann Arbor, MI, USA.
Xiang Zhou: University of Michigan, Ann Arbor, MI, USA.
Jian Kang: University of Michigan, Ann Arbor, MI, USA.
Max T Aung: University of Michigan, Ann Arbor, MI, USA.
Min Zhang: University of Michigan, Ann Arbor, MI, USA.
Wei Zhao: University of Michigan, Ann Arbor, MI, USA.
Belinda L Needham: University of Michigan, Ann Arbor, MI, USA.
Sharon L R Kardia: University of Michigan, Ann Arbor, MI, USA.
Yongmei Liu: Duke University, Durham, NC, USA.
John D Meeker: University of Michigan, Ann Arbor, MI, USA.
Jennifer A Smith: University of Michigan, Ann Arbor, MI, USA.
Bhramar Mukherjee: University of Michigan, Ann Arbor, MI, USA.
Causal mediation analysis aims to characterize an exposure's effect on an outcome and quantify the indirect effect that acts through a given mediator or a group of mediators of interest. With the increasing availability of measurements on a large number of potential mediators, like the epigenome or the microbiome, new statistical methods are needed to simultaneously accommodate high-dimensional mediators while directly target penalization of the natural indirect effect (NIE) for active mediator identification. Here, we develop two novel prior models for identification of active mediators in high-dimensional mediation analysis through penalizing NIEs in a Bayesian paradigm. Both methods specify a joint prior distribution on the exposure-mediator effect and mediator-outcome effect with either (a) a four-component Gaussian mixture prior or (b) a product threshold Gaussian prior. By jointly modeling the two parameters that contribute to the NIE, the proposed methods enable penalization on their product in a targeted way. Resultant inference can take into account the four-component composite structure underlying the NIE. We show through simulations that the proposed methods improve both selection and estimation accuracy compared to other competing methods. We applied our methods for an in-depth analysis of two ongoing epidemiologic studies: the Multi-Ethnic Study of Atherosclerosis (MESA) and the LIFECODES birth cohort. The identified active mediators in both studies reveal important biological pathways for understanding disease mechanisms.
