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Gene-environment correlation



Contents

Definition

The tendency for individuals to experience environments that are correlated with their genetic propensities is known as gene-environment correlation (or more accurately, genotype-environment correlation). Gene-environment correlations can arise by both causal and non-causal mechanisms. [1] Of principal interest are the causal mechanisms, which indicate genetic control over environmental exposure. Genetic variants influence environmental exposure indirectly via behavior. Three causal mechanisms giving rise to gene-environment correlations have been described. [2]

(i) Passive gene-environment correlation refers to the association between the genotype a child inherits from her parents and the environment in which the child is raised. Parents create a home environment that is influenced by their own heritable characteristics. Biological parents also pass on genetic material to their children. When the children's genotype also influences their behavioral or cognitive outcomes, the result can be a spurious relationship between environment and outcome. For example, because parents who have histories of antisocial behavior (which is moderately heritable) are at elevated risk of abusing their children, a case can be made for saying that maltreatment may be a marker for genetic risk that parents transmit to children rather than a causal risk factor for children’s conduct problems. [3]

(ii) Evocative (or reactive) gene-environment correlation happens when an individual's (heritable) behavior evokes an environmental response. For example, the association between marital conflict and depression may reflect the tensions that arise when engaging with a depressed spouse rather than a causal effect of marital conflict on risk for depression.

(iii) Active gene-environment correlation occurs when an individual possesses a heritable propensity to select environmental exposure. For example, individuals who are characteristically extroverted may seek out very different social environments than those who are shy and withdrawn.

Gene-environment correlation can also arise from non-causal mechanisms, including evolutionary processes and behavioral 'contamination' of the environmental measure. Evolutionary processes, such as genetic drift and natural selection, can cause allele frequencies to differ between populations. For example, exposure to malaria-bearing mosquitoes over many generations may have caused the higher allele frequency among certain ethnic groups for the sickle hemoglobin (HbS) allele, a recessive mutation that causes sickle-cell disease but confers resistance against malaria. [4] In this way, HbS genotype has become associated with the malarial environment.

Evidence

Twin and adoption studies have provided much of the evidence for gene-environment correlations by demonstrating that putative environmental measures are heritable. [5] For example, studies of adult twins have shown that desirable and undesirable life events are moderately heritable as are specific life events and life circumstances, including divorce, the propensity to marry, marital quality and social support. Studies in which researchers have measured child-specific aspects of the environment have also shown that putative environmental factors, such as parental discipline or warmth, are moderately heritable. Television viewing, peer group orientations and social attitudes have all been shown to be moderately heritable. There is also a growing literature on the genetic factors influencing behaviors that constitute a risk to health, such as the consumption of alcohol, tobacco and illegal drugs, and risk-taking behaviors. Like parental discipline, these health related behaviors are genetically influenced, but are thought to have environmentally mediated effects on disease. To the extent that researchers have attempted to determine why genes and environments are correlated, most evidence has pointed to the intervening effects of personality and behavioral characteristics.

Evidence for the existence of gene-environment correlations has recently started to accrue from molecular genetic investigations. The Collaborative Studies on Genetics of Alcoholism (COGA) group has reported that a single-nucleotide polymorphism in intron 7 of the gamma-aminobutyric acid A a2 receptor (rs279871; GABRA2) was associated with alcohol dependence and marital status. Individuals who had the high-risk GABRA2 variant (i.e., the variant associated with alcohol dependence) were less likely to be married, in part because they were at higher risk for antisocial personality disorder and were less likely to be motivated by a desire to please others. [6] There is also molecular evidence for passive gene-environment correlation. A recent study found that children were almost 2.5 times more likely to be diagnosed with attention-deficit hyperactivity disorder (ADHD) if their mothers were divorced, separated, or never married. In this sample, however, mothers possessing the short allele of the dopamine receptor gene DRD2 were more likely to be divorced, separated, or never married. Moreover, their children were more likely to have ADHD. Therefore, part of the association between parental marital status and ADHD diagnosis among children in this sample is due to the confounding variable of maternal DRD2 genotype. [7] Both of these studies also found evidence for gene-environment interaction.


References

  1. ^ Jaffee SR and Price TS (2007). "Gene-environment correlations: a review of the evidence and implications for prevention of mental illness.". Molecular Psychiatry 12 (5): 432-442. doi:10.1038/sj.mp.4001950. PMID 17453060.
  2. ^ Plomin R, DeFries JC, and Loehlin JC. (1977). "Genotype-environment interaction and correlation in the analysis of human behavior". Psychological Bulletin 84 (2): 309-322. PMID 557211.
  3. ^ DiLalla LF and Gottesman II. (1991). "Biological and genetic contributions to violence: Widom’s untold tale". Psychological Bulletin 109 (1): 125-129. PMID 2006224.
  4. ^ Aidoo M, Terlouw DJ, Kolczak MS, McElroy PD, ter Kuile FO, Kariuki S, Nahlen BL, Lal AA and Udhayakumar V (2002). "Protective effects of the sickle cell gene against malaria morbidity and mortality". Lancet 359 (9314): 1311-1312. doi:10.1016/S0140-6736(02)08273-9. PMID 11965279.
  5. ^ Kendler KS and Baker JH (2007). "Genetic influences on measures of the environment: a systematic review". Psychological Medicine 37 (5): 615-626. doi:10.1017/S0033291706009524. PMID 17176502.
  6. ^ Dick DM, Agrawal A, Schuckit MA, Bierut L, Hinrichs A, Fox L, Mullaney J, Cloninger CR, Hesselbrock V, Nurnberger JI Jr, Almasy L, Foroud T, Porjesz B, Edenberg H and Begleiter H (2006). "Marital status, alcohol dependence, and GABRA2: evidence for gene-environment correlation and interaction". J Stud Alcohol 67 (2): 185-194. PMID 16562401.
  7. ^ Waldman ID (2007). "Gene–environment interactions reexamined: Does mother’s marital stability interact with the dopamine receptor D2 gene in the etiology of childhood attention-deficit/hyperactivity disorder?". Development and Psychopathology 19: 1117–1128. doi:10.1017/S0954579407000570.

See also

  • Nature versus nurture
 
This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Gene-environment_correlation". A list of authors is available in Wikipedia.
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