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Variable selection for single-index varying-coefficients models with applications to synergistic G × E interactions.

Shunjie Guan1, Mingtao Zhao2, Yuehua Cui1

  • 1Department of Statistics and Probability, Michigan State University, East Lansing, MI, 48824, USA.

Electronic Journal of Statistics
|June 11, 2026
PubMed
Summary

This study introduces a new statistical method to identify synergistic gene-environment interactions (synG × E) that increase disease risk. The approach effectively selects important genetic and environmental factors involved in these complex interactions.

Keywords:
Primary 62J99, 60K35Variable selectionoracle propertysecondary 62P10single-index varying-coefficients modelsynergistic G × E interaction

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Area of Science:

  • Environmental Epidemiology
  • Statistical Genetics
  • Bioinformatics

Background:

  • Simultaneous exposure to multiple environmental risk factors (Es) can elevate disease risk beyond individual effects.
  • Synergistic gene-environment interactions (synG × E) describe how combined genetic and multiple environmental exposures impact disease risk.
  • Single-index varying-coefficients models (SIVCM) are used to analyze synG × E effects.

Purpose of the Study:

  • To propose a unified variable selection approach for SIVCM to model synG × E.
  • To estimate and select important genetic and environmental variables contributing to synergistic interactions.
  • To identify nonlinear synG × E, no synG × E, and no genetic effects.

Main Methods:

  • Developed a unified variable selection approach for SIVCM.
  • The method estimates varying, non-zero constant, and zero effects for gene variables.
  • Selected important environmental variables involved in synergistic interactions.
  • Theoretically evaluated the oracle property of the variable selection approach.

Main Results:

  • The proposed method effectively estimates and selects important variables for synG × E.
  • Simulation studies demonstrated strong finite sample performance for both continuous and discrete gene variables.
  • Application to a real dataset confirmed the method's practical utility.

Conclusions:

  • The developed approach provides a robust tool for identifying synergistic gene-environment interactions.
  • This method has broad applicability in research aiming to understand complex disease etiology.
  • It enables a deeper understanding of how multiple environmental exposures jointly influence genetic risks.