Uncovering the Heritable Components of Multimorbidities and Disease Trajectories: A Nationwide Cohort Study


Abstract

Quantifying the contribution of genetics and environmental effects on disease initiation and progression, as well as the shared genetics of different diseases, is vital for the understanding of the disease etiology of multimorbidities. In this study, we leverage nationwide Danish registries to provide a granular atlas of the genetic origin of disease phenotypes for a cohort of all Danes 1978-2018 with partially known pedigree (n = 6.3 million). We estimate the heritability and genetic correlation between thousands of disease phenotypes using a novel approach that can be scaled to nationwide data. Our findings confirm the importance of genetics for a number of known associations and increase the resolution of heritability by adding numerous novel associations, some of which point to shared biologically origin of different phenotypes. We also establish the heritability of disease trajectories and the importance of sex-specific genetic contributions.

 

ICD10 level 3:

Toggle columns:

Phenotype Code Variance Component ICD10 Code Description ICD10 Chapter Number ICD10 Chapter Name Median 95% CI Upper 95% CI Lower

Cite
If you use the information on this website or in the paper, please cite:

Uncovering the Heritable Components of Multimorbidities and Disease Trajectories: A Nationwide Cohort Study

David Westergaard, Frederik Hytting Jørgensen, Jens Waaben, Mette Lademann, Thomas Folkmann Hansen, Jolien Cremers, Sisse Rye Ostrowski, Ole Birger Vesterager Pedersen, Danish Blood Donor Study Genomic Consortium, Roc Requant, Isabella Friis Jørgensen, Tom Fitzgerald, Ewan Birney, Karina Banasik, Laust Mortensen, Søren Brunak

Link to article: https://www.medrxiv.org/content/10.1101/2023.02.08.23285642v1


Webmaster: Troels Siggaard (troels.siggaard[AT]cpr.ku.dk)