Abstract

BackgroundGene × environment models are widely used to assess genetic and environmental risks and their association with a phenotype of interest for many complex diseases. Mixed generalized linear models were used to assess gene × environment interactions with respect to systolic blood pressure on sibships adjusting for repeated measures and hierarchical nesting structures. A data set containing 410 sibships from the Framingham Heart Study offspring cohort (part of the Genetic Analysis Workshop 13 data) was used for all analyses. Three mixed gene × environment models, all adjusting for repeated measurement and varying levels of nesting, were compared for precision of estimates: 1) all sibships with adjustment for two levels of nesting (sibs within sibships and sibs within pedigrees), 2) all sibships with adjustment for one level of nesting (sibs within sibships), and 3) 100 data sets containing random draws of one sibship per extended pedigree adjusting for one level of nesting.ResultsThe main effects were: gender, baseline age, body mass index (BMI), hypertensive treatment, cigarettes per day, grams of alcohol per day, and marker GATA48G07A. The interaction fixed effects were: baseline age by gender, baseline age by cigarettes per day, baseline age by hypertensive treatment, baseline age by BMI, hypertensive treatment by BMI, and baseline age by marker GATA48G07A. The estimates for all three nesting techniques were not widely discrepant, but precision of estimates and determination of significant effects did change with the change in adjustment for nesting.ConclusionOur results show the importance of the adjustment for all levels of hierarchical nesting of sibs in the presence of repeated measures.

Highlights

  • Gene × environment models are widely used to assess genetic and environmental risks and their association with a phenotype of interest for many complex diseases

  • The Framingham Heart Study began in 1948 with the aim of gathering the longitudinal family data needed for a comprehensive study of genetic and environmental risks for cardiovascular disease

  • The main effects included in the model were: gender, baseline age, body mass index (BMI), hypertensive treatment, cigarettes per day, grams of alcohol per day, and marker GATA48G07A (heterozygote genotype with alleles 1 and 3 (57% of total individuals) contrasted with all other possible genotypes)

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Summary

Introduction

Gene × environment models are widely used to assess genetic and environmental risks and their association with a phenotype of interest for many complex diseases. Studies have examined environmental and genetic variables influencing blood pressure in the Framingham data as well as in other large epidemiologic data sets [3,4]. These studies were performed in extended pedigree, sibship, and case-control data. Genetic studies have found multiple regions on the genome that may contain a candidate gene for systolic blood pressure (SBP) and/or hypertension Among these regions are areas on chromosomes 10 and 17 [5,6]. Chromosome 17 contains the angiotensin-I converting enzyme (ACE) gene and there is good supporting evidence that this gene is involved in hypertension [7,8,9]

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