Intermountain Healthcare is building a new global DNA registry based on medical histories from people around the world, using existing genetic test results and electronic health histories.
The new DNA database, the GeneRosity Registry, will enable researchers to find genetic codes that determine who’s at risk of developing genetic health problems and help them quickly and economically.
To populate the registry, researchers from the Intermountain Medical Center Heart Institute are asking adults who’ve already purchased direct-to-consumer DNA testing at commercial sites like AncestryDNA, MyHeritage, or 23andMe to voluntarily upload their raw and unprocessed genetic results, or genotypes. Study funding was provided by donors to the Intermountain Research and Medical Foundation.
“Our project is creating a resource for future studies,” Stacey Knight, Ph.D., a cardiovascular and genetic epidemiologist at the Intermountain Medical Center Heart Institute, said. “A person’s DNA is made up of more than 3 billion individual pairs of genetic codes, but finding specific genes that contribute to health problems isn’t easy. That’s why we’re asking people to submit their DNA results, along with as much personal and family medical history as they know.”
A medical history is a record of health information about a person and their close relatives. A complete record includes information from three generations of relatives, including children, brothers and sisters, parents, aunts and uncles, nieces and nephews, grandparents, and cousins.
Families have many factors in common, including their genes, environment, and lifestyle. Together, these factors can give clues to medical conditions that may run in a family. By identifying patterns of disorders among relatives, medical researchers can determine whether an individual, other family members, or future generations may be at an increased risk of developing a condition.
“A family medical history can identify people with a higher-than-usual chance of having common disorders such as heart disease, high blood pressure, stroke, certain cancers, and diabetes,” Dr. Knight said. “These complex disorders are influenced by a combination of genetic factors, environmental conditions, and lifestyle choices.”
However, searching through genetic codes takes a lot of time and requires a lot of information from many people. The data collected for this project will allow researchers who participate in the registry to search more specifically for genetic markers related to what they’re studying.
“We’ll be able to use the information people submit to validate new genetic and disease findings, discover new genetic mutation and genetic profiles, and drive future studies,” said Dr. Knight. “If the GeneRosity Registry’s researchers are successful in future research using these data, others will benefit greatly.”
All of the information will be stored in a secure database accessed only by researchers involved in the GeneRosity Registry. People who are interested in participating should sign up on the project’s website at www.GeneRosityRegistry.org.
The Intermountain Research Foundation, which is part of the Intermountain Foundation, provides seed grant money for worthy research projects, such as this one, that lead to clinical applications.
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