In the largest genome-wide study of brain aneurysms ever conducted, an international team led by researchers at the Yale School of Medicine has identified three new genetic variants that increase a person's risk for developing this deadly disease. "These findings provide important new insights into the causes of intracranial aneurysms and are a critical step forward in the development of a diagnostic test that can identify people at high risk prior to the emergence of symptoms," said Dr. Murat Gunel, senior author of the report. "Given the often-devastating consequences of the bleeding in the brain, early detection can be the difference between life and death." The new study, the second by Yale researchers published within the last 15 months, brings to five the number of regions of the genome that have been found to contribute to the nearly 500,000 cases of this devastating disorder diagnosed annually worldwide. The researchers searched across the entire genome for changes in the genetic code that were shared more often by aneurysm patients than by unaffected individuals. The researchers determined that if persons carry all of the risk variants discovered by the Yale-led team, they are five to seven times more likely to suffer an aneurysm than those individuals who carry none. While these findings have transformed the understanding of the genetic risks for intracranial aneurysms, considerable work remains to be done, the researchers noted. "These five findings explain about 10 percent of genetic risk of suffering an aneurysm," Dr. Gunel said. "This is 10 percent more than we understood just a couple of years ago, but there is a long way to go."
Login Or Register To Read Full Story