- 26 areas of DNA have been identified as being involved in the development of epilepsy.
- The research is the largest genetic study of its kind and involved more than 150 researchers across the world.
- Experts say being able to better understand the genetic underpinnings of epilepsy could lead to more targeted treatments.
Specific changes in DNA may increase the risk of developing epilepsy.
That’s according to
In the study, researchers identified 26 areas of DNA involved in the development of epilepsy in addition to 29 genes that are likely contributing to epilepsy within those areas.
“Gaining a better understanding of the genetic underpinnings of epilepsy is key to developing new therapeutic options and consequently a better quality of life for the over
“The discoveries we report on here could only be achieved through international collaboration, on a global scale,” he added. “We are proud of how the global community of scientists working to better understand the genetics of the epilepsies have pooled resources and collaborated effectively, for the benefit of people impacted the condition.”
The new research is the largest genetic study of its kind and involved more than 150 researchers in North America, South America, Europe, Australia and Asia.
As part of the study, the researchers compared DNA from nearly 30,000 people living with epilepsy alongside DNA from more than 52,500 people without the condition.
The scientists were able to identify 26 distinct changes to the DNA in people living with epilepsy. They were also able to identify 19 changes in DNA that are specific to a type of epilepsy called genetic generalized epilepsy (GGE).
“This…
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