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Integration of latent factor analysis into multivariable Mendelian randomization
Yuankai Zhang1, Roby Joehanes2, Tianxiao Huan2
1Department of Biostatistics, Boston University School of Public Health, Boston, MA, USA. yukiz@bu.edu.
This study introduces a novel method for multivariable Mendelian randomization (MVMR) that effectively handles highly correlated exposures using latent factor analysis. The approach improves causal inference in complex multi-omics data, offering enhanced sensitivity and interpretability.
Area of Science:
- Genetics
- Epidemiology
- Bioinformatics
Background:
- Mendelian randomization (MR) uses genetic variants to infer causality from observational data.
- Multivariable MR (MVMR) extends this to multiple exposures but struggles with highly correlated exposures, especially in high-dimensional multi-omics data.
- Conventional MVMR methods can face multicollinearity and reduced power with correlated exposures, limiting biological insights.
Purpose of the Study:
- To develop an enhanced MVMR framework that addresses challenges posed by highly correlated exposures in high-dimensional settings.
- To integrate latent factor analysis into MVMR for effective dimension reduction while preserving interpretability.
- To improve causal inference in multi-omics studies by accounting for shared latent factors or pathways.
Main Methods:
- Proposed an integration of latent factor analysis within the MVMR framework.
- Developed a method for dimension reduction in MVMR without compromising biological interpretability.
- Validated the approach through extensive simulation studies.
Main Results:
- The proposed method demonstrated a well-controlled false positive rate in simulations.
- Achieved superior sensitivity compared to conventional MVMR approaches for correlated exposures.
- Successfully applied the method to investigate causal links between DNA methylation and mitochondrial DNA copy number.
Conclusions:
- The novel latent factor-based MVMR method effectively handles highly correlated exposures, particularly in multi-omics data.
- This approach offers significant advantages for uncovering causal relationships driven by shared latent factors or pathways.
- The method provides new insights into molecular mechanisms underlying complex phenotypes by improving causal inference in high-dimensional genetic data.
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