Evidence map›Paper›PMID 42541367›Full record

ArticleGenetic epidemiology2026

The Omnicausal Model Reveals the Highly Polyfactorial Nature of Complex Diseases.

Carla Márquez-Luna, Martin Tournaire, Ghislain Rocheleau, Ron Do, Marie Verbanck

Abstract read
In one paragraph

Article in Genetic epidemiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Carla Márquez-LunaThe Charles Bronfman Institute for Personalized Medicine, Icahn School of Medicine at Mount Sinai, New York, New York, USA.ORCID https://orcid.org/0000-0002-7083-5922
Martin TournaireUR 7537 BioSTM, Biostatistique, Traitement et Modélisation des données biologiques, Université Paris Cité, Paris, France.
Ghislain RocheleauThe Charles Bronfman Institute for Personalized Medicine, Icahn School of Medicine at Mount Sinai, New York, New York, USA.ORCID https://orcid.org/0000-0002-9989-7553
Ron DoThe Charles Bronfman Institute for Personalized Medicine, Icahn School of Medicine at Mount Sinai, New York, New York, USA.ORCID https://orcid.org/0000-0002-3144-3627
Marie VerbanckUR 7537 BioSTM, Biostatistique, Traitement et Modélisation des données biologiques, Université Paris Cité, Paris, France.ORCID https://orcid.org/0000-0002-1669-572X

Funding

Towards an integrated map of causal connections for common, complex diseasesR35GM124836 · NIGMS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Ron Do · 2017 to 2026
$3.9M
Elucidating hereditary transthyretin-mediated heart failure risk using machine learning, polygenic risk and recall by genotype approaches in African ancestry individualsR01HL155915 · NHLBI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI DO, RON, NADKARNI, GIRISH NITIN · 2021 to 2024
$3.4M
Resolving Causal Influences Among Correlated Risk Biomarkers for Coronary Artery DiseaseR01HL139865 · NHLBI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI DO, RON · 2018 to 2021
$1.7M
Bettencourt Schueller foundation and the EURIP graduate program ANR-17-EURE-0012Carla Marquez Luna NIH5T32HL00782424French National Research Agency (ANR) ANR-21-CE45-0023-01National Heart, Lung, and Blood Institute of the NIH R01-HL139865National Heart, Lung, and Blood Institute of the NIH R01-HL155915National Institute of General Medical Sciences of the National Institutes of Health (NIH) R35-GM124836NHLBI NIH HHS R01 HL139865NHLBI NIH HHS R01 HL155915NIGMS NIH HHS R35 GM124836
6 · The paper itself

Abstract

Mendelian randomization (MR) is a human genetics method for inferring causal relationships between risk factors and diseases. A common focus of MR studies has been on the causal inference of a single risk factor on a single disease. This has led to the successful discovery of numerous causal risk factors for disease. However, it remains unclear how much each causal risk factor contributes to disease collectively. Here, we introduce the concept of "causality explained," that provides an estimator of the causal variance explained by a phenome-wide set of risk factors on complex diseases to assess how much causality can be potentially explained. The model is based on principal component regression which is a multivariate linear regression based on principal component analysis. In complement, we propose the "polyfactorial index" to assess the trajectory of causality explained as risk factors are sequentially added into the model, to characterize the causal architecture for a complex disease. We demonstrate that our model correctly assesses the causality explained and causal architecture in simulations across a wide range of parameters. To build our model, we used a phenome-wide set of 222 traits from the UK Biobank compared to a set of 5 known risk factors for coronary artery disease. We observed that the phenome-wide set explains more than 45% of causality compared to 28.76% for the set of known risk factors. In addition, we tested our approach on 13 complex diseases and showed that the phenome-wide set can explain between 27% for anorexia to 80% for schizophrenia, with ever increasing trajectories of causality explained. We propose the "omnicausal model," which posits that a large number of risk factors individually explains a small amount to disease but collectively explain most of the causal variance. We distinguished core and peripheral causal factors that explain respectively a larger and a smaller part of causal variance. This approach provides insights into the underlying causal architecture between risk factors and disease.

Indexed as

Mendelian Randomization AnalysisModels, GeneticCausalityComputer SimulationGenetic Predisposition to DiseaseHumansPhenotypePrincipal Component AnalysisRisk FactorsSchizophreniacausality explainedcomplex diseasesMendelian randomizationomnicausal modelphenome‐wide risk factorspolyfactorial index

Identifiers

PMID42541367
PMCPMC13428326

What Socratic holds

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LicenceCC BY-NC-ND
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.