Approaches for Investigating Gene-Environment Interactions€¦ · • Gene Environment...
Transcript of Approaches for Investigating Gene-Environment Interactions€¦ · • Gene Environment...
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Assistant Professor Institute for Computational Biology Department of Epidemiology and Biostatistics Case Western Reserve University
Approaches for Investigating Gene-Environment Interactions
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Acknowledgements
• A BIG thanks to Dr. Dana Crawford for providing many examples and slides for this presentation
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What is an Interaction?
• Effect of one factor depends on the level of another factor (effect modi"cation)
• A Biologist’s View • A Statistician’s View
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Gene Environment Interaction
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Garrod Lancet 2:1616-1620 (1902)
Alkaptonuria (AKU): n Inborn error of metabolism n Autosomal recessive n Urine is dark, depending on
diet
Sir Archibald Garrod
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Gene Environment Interaction
• Phenylketonuria (PKU): Need BOTH risk genotype and exposure
• Xeroderma pigmentosum (XP): Can develop skin cancer with exposure, but risk is much greater with risk genotype AND exposure
• Emphysema: Can develop disease with exposure (smoking) or risk genotype (α-antitrypsin), but risk is much greater with BOTH
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Gene Environment Interactions
• How do we identify gene-environment interactions?
• Need Exposures AND Genotypes
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Gene Environment Interactions
Common “environmental” exposures: • Smoking/tobacco use (ETS) • Diet • Medication use • Occupation • Household environment • Physical activity
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Gene Environment Interaction
• Regional exposures
• Geographic Information Systems (GIS)
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Friedman et al JAMA 285(7):897-905
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Collecting Exposures
• Ask participant about past exposures (surveys) • Ask the participant’s physician or pharmacist
about past exposures (EMR, medication lists) • Measure the exposure in blood, urine • Ask participant to take medication, to exercise,
etc
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Collecting Exposures
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Retrospective
Prospective
Manolio, Bailey-Wlson, Collins Nat Genet Review 7:812-820 (2006)
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Retrospective Studies
• In a retrospective study, mothers who have infants with birth defects (cases) may “over recall” past exposures compared with mothers who have infants with no birth defects (controls)
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Werler et al Am J Epidemiol 129:415-421 (1989)
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Bias • All studies are subject to some kind of bias
• All studies may have inaccurate exposure assessment
• Examples: Height and weight (BMI) Energy intake Family history Smoking status
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Bias in Self-report Height • Self-report vs measured
(from NHANES III)
• Older individuals under report actual height
• Other studies suggest weight discrepancy is associated with gender, age, race/ethnicity, and BMI (Villanueva et al 2001)
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Kuczmarski, Kuczmarski, Najjar J Am Diet Assoc 101:28-34 (2001)
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Under-reporting Energy Intake
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Briefel et al Am J Clin Nutr 65(suppl):1203S-1209S (2007)
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Timing of Exposure is Important
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Ober and Vercelli Trends in Genetics (2011)
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Detection Strategies
• Stratify by Exposure and Genotype • Include an Interaction Term in a Statistical
Model • Analysis of Covariance • Mixed Model Approaches
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Stratified Analyses
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Example of “pharmacogenetics”
Hunter Nat Genet Review 6:287-298 (2005)
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Replication can be Difficult
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Cross, Poole, Ulrich Pharmacogenomics J 8:237-47(2008)
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FTO and Physical Activity
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Demerath et al Obesity (Silver Spring) 19(9):1866-1872 (2011)
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Analysis of Covariance
• Similar to ANOVA • Examines relationships between two continuous
variables across continuous categories • Null hypothesis = slopes are equal across all
categories
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Analysis of Covariance • Band A:
Low fat intake and TT genotype Associated with high HDL
• Band B: Moderate fat intake and TT No association with HDL
• Band C: High fat intake and TT genotype Associated with low HDL
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Manolio, Bailey-Wilson, Collins Nat Genet Review 7:812-820 (2006)
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Mixed Model Analysis
• Allows estimation of the Proportion of Trait Variance Explained (PVE) using GWAS data
• Relates genetic similarity to phenotypic similarity
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Yang et al. Am J Hum Genet 88(1):76-82
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Mixed Model Analysis
• Mixed Models can include interaction terms to test for global genetic X environmental factor interaction
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Zheng et al. PLoS ONE 8:10(2013)
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Difficulties with these Strategies
• Requires good exposure information
• Can be subject to bias (study design)
• Need large sample sizes
• Limited methods to identify all higher-order interactions
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Conclusions
• Gene Environment Interactions are likely an important part of the genetic architecture of human disease
• Systematically collecting environmental exposures in a manner to allows their identi"cation is the primary challenge
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