"This paper calls attention to the potential importance of epigenetic factors that can influence the risk of complex diseases," said Montgomery Slatkin, the researcher who devised the study, and a professor at the University of California, Berkeley's Department of Integrative Biology, "and to the need to identify such factors and determine their rate of gain and loss."
The model described in the report represents a first step in quantifying the effect of epigenetic change on disease risk and recurrence risk. It found that while mutations have the largest effect on disease risk heritability, epigenetic factors play a surprisingly large role in the disease risk that gets passed down through the generations. Several other studies have already suggested that environmental factors, such as a pregnant woman's diet, might lead to epigenetic changes in her offspring, making it imperative for researchers and public health officials to understand exactly how these epigenetic factors and their causes influence disease risk.
"Almost every article on disease heritability describes 'genetics' as being an important factor in a person's likelihood to contract disease," said Mark Johnston, Editor-in-Chief of the journal GENETICS. "Indeed that is true, but what is not often explained is that less permanent changes to our DNA also significantly influence our risk for disease. We tend to view disease risk as a tug of war between nature and nurture, but this study shows that nature and nurture are more closely related than we had imagined."