The causes of type 2 diabetes are a combination of heredity and environment. However, only up to 15 percentage of the heredity can be explained by genetic factors discovered till date.
Leif Groop, the Lund University professor responsible for the new study, has contributed to a large extent to our current knowledge about heredity and type 2 diabetes. He participated in the first major genetic mapping presented in 2012, which identified a large number of risk genes for type 2 diabetes. He was also part of a Finnish study which showed in 1996 that the hereditary risk is greater if the mother has type 2 diabetes.
The new study combines knowledge from the previous investigations with new genetic analyses of families in which one parent and a child suffer from type 2 diabetes. The findings from the study explain how the heredity of the disease is passed down within families, whether it comes from the mother or the father. The researchers used data and DNA gathered from two of the world’s largest family studies, the Botnia study in Finland and the Transdanubian Biobank in Hungary. In total, around 4000 families were included in the study of which 2000 were used for the current study.
The results show that the variations in two previously identified risk genes for type 2 diabetes, KCNQ1 and THADA, cause an increased risk of acquiring the disease in the child if they are inherited from the mother (known as the parent-of-origin effect). Inheriting the risk genes from the father, on the other hand, has less or no effect on the risk of disease for the child.
Researchers have previously identified the role of KCNQ1 in heredity between mother and child.
“THADA proved to play an even more important role in the transfer of heredity from the mother to the child, and this was previously completely unknown”, says Rashmi Prasad, responsible for the analyses.
According to the researchers, the fact that the genes inherited from the mother affect the risk of disease probably depends on the genes from the father being silenced in a process known as imprinting. Age and environmental factors expose the genes to chemical changes, known as methylation, which affect their function and in some cases silence the genes.
Thus the lifestyle of the mother, with factors such as stress, diet, illness etc., probably affects the future risk of disease in the foetus.
“Even if the father’s lifestyle also affects the future child to some extent, the foetus is exposed for a longer time in utero and during breast-feeding to the influence of the mother’s life and habits. This could explain why heredity from the mother has a greater effect on the child’s genome”, says Leif Groop.
The findings are published in the scientific journal Diabetologia and in an overview of heredity in type 2 diabetes.
Facts: Heredity and type 2-diabetes
Type 2 diabetes develops when blood sugar levels are too high over a long time, leading to damage to the eyes, nerves, kidneys and cardiovascular disease.
With type 2 diabetes in the family, the risk of an individual developing the disease is three times higher. The risk is greater if the mother has the disease than if the father suffers from it.
There are currently over 120 known genetic risk variants associated with type 2 diabetes as they affect the ability of cells to produce or respond to the blood sugar-regulating hormone insulin.
