Intermountain Healthcare is creating a new global DNA registry based on medical histories from people around the world, which researchers can use to find genetic codes that determine who’s at risk of developing genetic health problems and help them quickly and economically.
Researchers from the Intermountain Medical Center Heart Institute are seeking existing genetic test results and electronic health histories to form a new worldwide database called the GeneRosity Registry.
To populate the registry, they’re 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.
Dr. Jeffrey Anderson, is a distinguished research physician at Intermountain Medical Center Heart Institute. He’s used to enrolling his patients in studies but this time, it’s he and his family taking part in the study.
“interesting to have the tables turned on me.”
For christmas the family got the gift of AncestryDNA, the website, like others such as MyHeritage or 23andMe, provide dna testing.
“my family, my wife has a lot of interest in where the roots of my family come from.”
Dr. Stacey Knight with Intermountain Medical Center Heart Institute is hoping those who have already purchased the direct to consumer DNA testing would be willing to share their information.
Dr. Knight, “we’re asking those individuals to take the raw files, upload it into our registry so we can use it for doing medical research. It will help us understand more on causes for diseases and how to better treat diseases based on their genetic profile.”
Dr. Anderson, “there only a small amount used to tell which country your ancestors come from, why not use the rest of that. You’ve already paid for the test why not take advantage of all that information that’s not being used.”
Dr. Knight “we are having medical breakthroughs on a daily basis because of the rapid increase in knowing an individual’s genetics. Those advances are translating to better care for patients. I see it as an opportunity to start a dialogue about family health and the genetics and how we can as a family take better care of our health.”
Experts from the Heart Institute kicked off the new registry will be at RootsTech 2018 conference. RootsTech is a a global family history event where people use technology to discover and share their family connections across generations.
Researchers are hoping to reach a wide audience to start the conversation about what benefits sharing existing results can have not only for people today, but future generations. Study funding was provided by donors to the Intermountain Research and Medical Foundation.
“Our project is creating a resource for future studies,” said Stacey Knight, PhD, MStat, a cardiovascular and genetic epidemiologist at the Intermountain Medical Center Heart Institute. “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 particular 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. Contributors to the registry don’t have to submit lab samples, take medications, or complete any procedures in order to participate. The project is conducted completely online and doesn’t require any study-related visits or phone calls.
People who are interested in participating should sign up on the project’s website at www.GeneRosityRegistry.org. On the website, participants will be asked to do the following:
• Watch a short video explaining the project and agree to participate
• Provide their name and contact information
• Answer a few questions
• Upload their raw genetic data
• Fill out a personal and family health history using a health-related family tree application
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.
This article contains sponsored content.