Abstract
The role of twins in research is evolving as we move further into the post-genomic era. With the re-definition of what a gene is, it is becoming clear that biological family members who share a specific genetic variant may well not have a similar risk for future disease. This has somewhat invalidated the prior rationale for twin studies. Case co-twin study designs, however, are slowly emerging as the ideal tool to identify both environmentally induced epigenetic marks and epigenetic disease-associated processes. Here, we propose that twin lives are not as identical as commonly assumed and that the case co-twin study design can be used to investigate the effects of the adult social environment. We present the elements in the (social) environment that are likely to affect the epigenome and measures in which twins may diverge. Using data from the German TwinLife registry, we confirm divergence in both the events that occur and the salience for the individual start as early as age 11. Case co-twin studies allow for the exploitation of these divergences, permitting the investigation of the role of not only the adult social environment, but also the salience of an event or environment for the individual, in determining lifelong health trajectories. In cases like social adversity where it is clearly not possible to perform a randomised-controlled trial, we propose that the case co-twin study design is the most rigorous manner with which to investigate epigenetic mechanisms encoding environmental exposure. The role of the case co-twin design will continue to evolve, as we argue that it will permit causal inference from observational data.
Highlights
Lifelong health trajectories are influenced by social and societal variables that are subsequently encoded in the epigenome
Summing up all single health indicators, for approximately one third of MZ twins one of the twins reports at least one health impairment, and the other one does not
In this paper we develop the hypothesis that the case co-twin study paradigm may be an elegant manner in which to evaluate the epigenetic and long-term health effects of the adult social environment
Summary
Lifelong health trajectories are influenced by social and societal variables that are subsequently encoded in the epigenome. The role of the social environment in health trajectories is confounded since the magnitude and relevance of their association varies at different ages and stages of disease progression This is highlighted by the case of breast cancer. We present preliminary evidence that twin lives are not as identical as previously assumed, and that they show sufficient divergence in life experiences so that they can provide an ideal study-pair matched for sex, age, genetics, developmental environment to examine the role of the adult social environment. This in turn will help identify both environmentally induced epigenetic marks and epigenetic disease-associated processes
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