The Omnicausal Model Reveals the Highly Polyfactorial Nature of Complex Diseases

Carla Márquez-Luna1,2, Martin Tournaire3, Ghislain Rocheleau1,2

  • 1The Charles Bronfman Institute for Personalized Medicine, Icahn School of Medicine at Mount Sinai, New York, New York, USA.

Genetic Epidemiology
|August 1, 2026
PubMed

Insights

Mendelian randomization (MR) can now quantify how much causality is explained by multiple risk factors for complex diseases. A phenome-wide approach reveals that numerous factors collectively explain significant disease variance, supporting the omnicausal model.

Area of Science:

  • Human genetics
  • Complex disease epidemiology
  • Statistical genetics

Background:

  • Mendelian randomization (MR) traditionally focuses on single risk factor-disease associations.
  • The collective contribution of multiple risk factors to complex diseases remains largely unquantified.
  • Understanding the causal architecture of diseases is crucial for effective prevention and treatment.

Purpose of the Study:

  • To develop a method for estimating the proportion of causal variance explained by a comprehensive set of risk factors for complex diseases.
  • To introduce the "causality explained" estimator and the "polyfactorial index" to characterize disease causal architecture.
  • To test the "omnicausal model" proposing that numerous factors collectively explain disease variance.

Main Methods:

  • Utilized principal component regression, a multivariate linear regression technique based on principal component analysis.
  • Applied a phenome-wide set of 222 traits from the UK Biobank.
  • Developed the "polyfactorial index" to assess the cumulative effect of sequentially added risk factors.

Main Results:

  • The phenome-wide set of risk factors explained over 45% of causality for coronary artery disease, compared to 28.76% for known factors.
  • Applied to 13 complex diseases, the phenome-wide set explained between 27% (anorexia) and 80% (schizophrenia) of causal variance.
  • Demonstrated increasing "causality explained" trajectories as more risk factors were included, supporting the omnicausal model.

Conclusions:

  • The "causality explained" estimator and "polyfactorial index" effectively assess disease causal architecture.
  • The "omnicausal model" is supported, suggesting that complex diseases result from the collective effect of numerous small-effect risk factors.
  • This approach provides novel insights into the complex interplay of risk factors in disease etiology.

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