Estimating heritability and genetic correlations from large health datasets in the absence of genetic data

Abstract

Typically, estimating genetic parameters, such as disease heritability and between-disease genetic correlations, demands large datasets containing all relevant phenotypic measures and detailed knowledge of family relationships or, alternatively, genotypic and phenotypic data for numerous unrelated individuals. Here, we suggest an alternative, efficient estimation approach through the construction of two disease metrics from large health datasets: temporal disease prevalence curves and low-dimensional disease embeddings. We present eleven thousand heritability estimates corresponding to five study types: twins, traditional family studies, health records-based family studies, single nucleotide polymorphisms, and polygenic risk scores. We also compute over six hundred thousand estimates of genetic, environmental and phenotypic correlations. Furthermore, we find that: (1) disease curve shapes cluster into five general patterns; (2) early-onset diseases tend to have lower prevalence than late-onset diseases (Spearman’s ρ = 0.32, p –16); and (3) the disease onset age and heritability are negatively correlated (ρ = −0.46, p –16).

Document Details

Document Type
Pub Defense Publication
Publication Date
Dec 03, 2019
Source ID
10.1038/s41467-019-13455-0

Entities

People

  • Anders Boeck Jensen
  • Andrey Rzhetsky
  • David R. Blair
  • Gengjie Jia
  • Gustaf Edgren
  • Hanxin Zhang
  • Ishanu Chattopadhyay
  • Lea Karatheodoris Davis
  • Mikael Benson
  • Nancy J. Cox
  • Peter Robinson
  • Søren Brunak
  • Torsten Dahlén
  • Xin Gao
  • Yu Li

Organizations

  • Army Research Office

Tags

Fields of Study

  • Biology

Readers

  • Neural Network Machine Learning.
  • Regression Analysis.
  • Women's Health and Cancer Risk Research: African American Women and Pregnancy Outcomes.

Technology Areas

  • Biotechnology