Multi-level Latent Variable Models for Coheritability Analysis in Electronic Health Records

TL;DR

This paper introduces a multi-level latent variable modeling framework for estimating heritability and coheritability in EHR data, effectively capturing complex familial and phenotypic structures.

Contribution

It presents a novel, scalable statistical approach using multi-level latent variables and GEE algorithms for joint heritability and genetic correlation estimation in diverse phenotypes.

Findings

Identified significant genetic correlations between mental health and metabolic phenotypes.

Demonstrated estimator consistency and validity through simulation studies.

Applied method to real EHR data revealing shared genetic influences.

Abstract

Electronic health records (EHRs) linked with familial relationship data offer a unique opportunity to investigate the genetic architecture of complex phenotypes at scale. However, existing heritability and coheritability estimation methods often fail to account for the intricacies of familial correlation structures, heterogeneity across phenotype types, and computational scalability. We propose a robust and flexible statistical framework for jointly estimating heritability and genetic correlation among continuous and binary phenotypes in EHR-based family studies. Our approach builds on multi-level latent variable models to decompose phenotypic covariance into interpretable genetic and environmental components, incorporating both within- and between-family variations. We derive iteration algorithms based on generalized equation estimations (GEE) for estimation. Simulation studies under various parameter configurations demonstrate that our estimators are consistent and yield valid inference across a range of realistic settings. Applying our methods to real-world EHR data from a large, urban health system, we identify significant genetic correlations between mental health conditions and endocrine/metabolic phenotypes, supporting hypotheses of shared etiology. This work provides a scalable and rigorous framework for coheritability analysis in high-dimensional EHR data and facilitates the identification of shared genetic influences in complex disease networks.