Introduction and Overview of Statistical Approaches to Gene × Environment Interactions for Complex Phenotypes

Author(s):  
Michael Windle

This chapter provides an introduction and overview of important issues that served as motivations for this book. For many complex phenotypes (e.g., depression, diabetes, obesity, substance use), there is substantial evidence that while genetic influences are important, so are environmental influences; moreover, there is substantial evidence from both behavior genetic studies (e.g., twin and adoptee studies) and molecular genetic studies (both human and infrahuman) that genes commonly interact with environmental factors in predicting complex phenotypes. The fields of genomics and other –omics (e.g., proteomics, metabolomics) provide exciting opportunities to advance science and foster the goals of public health and a more individualized intervention approach (e.g., precision medicine). The goals of these more individualized approaches would benefit greatly not only by advances in genomics and other –omics, but also by incorporating information both on environments and their interactions with genomic and other biological material and regulatory processes (e.g., environmental signal to biological pathway responses). Such findings would thereby offer more flexible guidance to a broader range of prevention, intervention, and treatment targets, and facilitate more tailored programs based on a fuller complement of G and E influences.

2013 ◽  
Vol 25 (1) ◽  
pp. 175-191 ◽  
Author(s):  
Caroline W. Oppenheimer ◽  
Benjamin L. Hankin ◽  
Jessica L. Jenness ◽  
Jami F. Young ◽  
Andrew Smolen

AbstractGene–environment correlations (rGE) have been demonstrated in behavioral genetic studies, but rGE have proven elusive in molecular genetic research. Significant gene–environment correlations may be difficult to detect because potential moderators could reduce correlations between measured genetic variants and the environment. Molecular genetic studies investigating moderated rGE are lacking. This study examined associations between child catechol-O-methyltransferase genotype and aspects of positive parenting (responsiveness and warmth), and whether these associations were moderated by parental personality traits (neuroticism and extraversion) among a general community sample of third, sixth, and ninth graders (N = 263) and their parents. Results showed that parent personality traits moderated the rGE association between youths' genotype and coded observations of positive parenting. Parents with low levels of neuroticism and high levels of extraversion exhibited greater sensitive responsiveness and warmth, respectively, to youth with the valine/valine genotype. Moreover, youth with this genotype exhibited lower levels of observed anger. There was no association between the catechol-O-methyltransferase genotype and parenting behaviors for parents high on neuroticism and low on extraversion. Findings highlight the importance of considering moderating variables that may influence child genetic effects on the rearing environment. Implications for developmental models of maladaptive and adaptive child outcomes, and interventions for psychopathology, are discussed within a developmental psychopathology framework.


CNS Spectrums ◽  
2006 ◽  
Vol 11 (12) ◽  
pp. 931-939 ◽  
Author(s):  
Daniela S.S. Lobo ◽  
James L. Kennedy

ABSTRACTBehavioral addictions are considered as the repetitive occurrence of impulsive behaviors without consideration of their potential negative consequences. These addictions represent an increasing cost to society and are an important new field of research in psychiatric genetics. There has been a growing body of evidence on the familial aggregation and genetic influences on the development of behavioral addictions and mainly on pathological gambling. The aim of this article is to critically review findings of family and molecular genetic studies on behavioral addictions, focusing on pathological gambling and commenting on other disorders where appropriate. This review provides a comprehensive approach to genetic studies on behavioral addiction and points out the necessity of expanding the genetic research in this field. Future directions for genetic studies in this field are also discussed.


Author(s):  
Ted Reichborn-Kjennerud ◽  
Kenneth S. Kendler

This chapter reviews the evidence for genetic contributions to the etiology of personality disorders (PDs) as defined by the Diagnostic and Statistical Manual of Mental Disorders (DSM; 5th ed.). This approach and some of the controversial issues associated with its development are briefly described in the first section. The second section evaluates the evidence for genetic influence on DSM PDs from family and twin studies using quantitative genetic methods. Studies that move beyond individual PDs are also reviewed, together with studies on the extent to which common genetic factors influence PDs and normal personality traits and PDs and pathological personality trait domains. Stability of genetic influences on PDs over time are also examined. Molecular genetic studies are reviewed in the third section. The fourth section deals with gene environment interplay, and the final section discusses future directions in the exploration of genetic influences on PDs.


2021 ◽  
pp. 164-186
Author(s):  
Benjamin B. Lahey

This chapter summarizes the basic biology of inheritance, including chromosomes, genes, nucleotides, genotype, and gene expression. It uses these concepts and the logic of studies of the two kinds of twins—monozygotic and dizygotic—to define the concept of heritability as the proportion of differences on the dimension among people in the population that is attributable to genetic factors. The genetic variance in the phenotypes of psychological problems, such as depression, is never encoded in a single allele or genetic variant. Rather, every dimension of psychological problems is polygenic, meaning that many genetic variants have very small genetic influences on each dimension of psychological problems that must be combined to meaningfully measure the genetic component of risk at the molecular level. Often, single variations in individual nucleotides—the molecules arranged on DNA that serve as the letters of the genetic code—known as single nucleotide polymorphisms are summed to quantify the molecular genetic risk in a polygenic risk score. The nonspecific genetic influences at the top of the hierarchy of genetic influences result from some genetic variants being pleiotropic in the sense of directly or indirectly influencing essentially all dimensions of psychological problems. Identifying the specific genetic and environmental influences on dimensions of psychological problems at each level of the hierarchy is complicated because they operate together through the crucially important gene–environment correlations and interactions described in this chapter.


Author(s):  
Tina Kretschmer ◽  
Matt DeLisi

This chapter reviews important strands of research on the heritability of antisocial behavior and crime, including both quantitative genetic studies using twin or adoption designs as well as molecular genetic approaches. Study designs are introduced and findings discussed. Contemporary avenues including gene-environment interplay and developmental models are presented. Overall it is concluded that a significant amount of variance in antisocial behavior and crime is attributable to genetic factors but conclusive knowledge on involvement of specific genes still absent. We conclude with a discussion of usage of genetic information in the criminal justice system and note future tasks for the field of bio-criminology.


Author(s):  
Tracey D. Wade ◽  
Cynthia Bulik

The current chapter reviews our progress in understanding how genes influence eating disorders by addressing the following areas: (1) how recognition of genetic influences on eating disorders emerged; (2) the complexities of gene environment interplay; (3) what twin studies can tell us about gene environment interplay, and (4) the current state of molecular genetic studies. It is concluded that both genes and nonshared environment play a critical role in the explanatory framework for the etiology of eating disorders. Shared environment is likely to contribute to the development of cognition and attitudes that may initiate disordered eating practices. Researchers are on the cusp of identifying specific genes that are implicated, and explication of the manner in which genes and the environment work together to increase risk for eating disorders hinges on the collection of larger samples.


Author(s):  
Michael J. Lyons ◽  
Chandra A. Reynolds ◽  
William S. Kremen ◽  
Carol E. Franz

The rapidly increasing number of people age 65 and older around the world has important implications for public health and social policy, making it imperative to understand the factors that influence the aging process. Twin studies can provide information that addresses critical questions about aging. Twin studies capitalize on a naturally occurring experiment in which there are some pairs of individuals who are born together and share 100% of their segregating genes (monozygotic twins) and some pairs that share approximately 50% (dizygotic twins). Twins can shed light on the relative influence of genes and environmental factors on various characteristics at various times during the life course and whether the same or different genetic influences are operating at different times. Twin studies can investigate whether characteristics that co-occur reflect overlapping genetic or environmental determinants. Discordant twin pairs provide an opportunity for a unique and powerful case-control study. There are numerous methodological issues to consider in twin studies of aging, such as the representativeness of twins and the assumption that the environment does not promote greater similarity within monozygotic pairs than dizygotic pairs. Studies of aging using twins may include many different types of measures, such as cognitive, psychosocial, biomarkers, and neuroimaging. Sophisticated statistical techniques have been developed to analyze data from twin studies. Structural equation modeling has proven to be especially useful. Several issues, such as assessing change and dealing with missing data, are particularly salient in studies of aging and there are a number of approaches that have been implemented in twin studies. Twins lend themselves very well to investigating whether genes influence one’s sensitivity to environmental exposures (gene-environment interaction) and whether genes influence the likelihood that an individual will experience certain environmental exposures (gene-environment correlation). Prior to the advent of modern molecular genetics, twin studies were the most important source of information about genetic influences. Dramatic advances in molecular genetic technology hold the promise of providing great insight into genetic influences, but these approaches complement rather than supplant twin studies. Moreover, there is a growing trend toward integrating molecular genetic methods into twin studies.


2015 ◽  
Vol 14 (6) ◽  
pp. 94-102
Author(s):  
Ye. Yu. Bragina ◽  
M. B. Freidin

This review focuses at the problem of the genetic basis of comorbidity. We discuss the concepts and terms relating to combinations of diseases. The guidelines of the study of comorbidity using modern high throughput methods and approaches of genetics, molecular biology and bioinformatics are designated. In this review we present results of studies showing genetic specificity for the combined phenotypes dif-ferent from the isolated disease, we considergene-gene and gene-environment interactions in comorbidity. We also discuss the role of single nucleotide polymorphisms and structural genome variations in the development of comorbidity. Own results of researching shared genes of inversely comorbid diseases like as bronchial asthma and tuberculosis are presented.


Sign in / Sign up

Export Citation Format

Share Document