Evidence map›Paper›PMID 39589697›Full record

ArticleBehavior genetics2025

On the Detection of Population Heterogeneity in Causation Between Two Variables: Finite Mixture Modeling of Data Collected from Twin Pairs.

Philip B Vinh, Brad Verhulst, Hermine H M Maes, Conor V Dolan, Michael C Neale

Abstract read
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Article in Behavior genetics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Philip B VinhDepartment of Human and Molecular Genetics, Virginia Commonwealth University, Richmond, USA. vinhpb@vcu.edu.ORCID 0000-0002-5292-0998
Brad VerhulstDepartment of Psychiatry and Behavioral Sciences, Texas A&M University, College Station, USA.ORCID 0000-0001-5369-9757
Hermine H M MaesDepartment of Human and Molecular Genetics, Virginia Commonwealth University, Richmond, USA.ORCID 0000-0001-7489-2214
Conor V DolanDepartment of Biological Psychology, Vrije Universiteit, Amsterdam, Netherlands.ORCID 0000-0002-2496-8492
Michael C NealeVirginia Institute for Psychiatric and Behavioral Genetics, Virginia Commonwealth University, Richmond, VA, USA.ORCID 0000-0003-4887-659X

Funding

Research Training: Psychiatric &Statistical GeneticsT32MH020030 · NIMH · VIRGINIA COMMONWEALTH UNIVERSITY · PI HERMINE H MAES, MICHAEL CHURTON NEALE · 1999 to 2026
$6.7M
Extensions of Mendelian Randomization Methodology for Combined Genomic and Methylomic AnalysisR01DA049867 · NIDA · VIRGINIA COMMONWEALTH UNIVERSITY · PI NEALE, MICHAEL CHURTON · 2020 to 2024
$1.9M
NIDA NIH HHS 5R01DA049867NIDA NIH HHS R01 DA049867NIMH NIH HHS 5T32MH020030NIMH NIH HHS T32 MH020030
6 · The paper itself

Abstract

Causal inference is inherently complex and relies on key assumptions that can be difficult to validate. One strong assumption is population homogeneity, which assumes that the causal direction remains consistent across individuals. However, there may be variation in causal directions across subpopulations, leading to potential heterogeneity. In psychiatry, for example, the co-occurrence of disorders such as depression and substance use disorder can arise from multiple sources, including shared genetic or environmental factors (common causes) or direct causal pathways between the disorders. A patient diagnosed with two disorders might have one recognized as primary and the other as secondary, suggesting the existence of different types of comorbidity. For example, in some individuals, depression might lead to substance use, while in others, substance use could lead to depression. We account for potential heterogeneity in causal direction by integrating the Direction of Causation (DoC) model for twin data with finite mixture modeling, which allows for the calculation of individual-level likelihoods for alternate causal directions. Through simulations, we demonstrate the effectiveness of using the Direction of Causation Twin Mixture (mixDoC) model to detect and model heterogeneity due to varying causal directions.

Indexed as

CausalityModels, StatisticalComputer SimulationDepressionHumansModels, GeneticSubstance-Related DisordersTwinsCausalityMixture modelingStatistical modelingTwin design

Identifiers

PMID39589697
PMCPMC11790744

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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 OpenQuestion graph.