San Francisco, United States – Two years after personal genetics startup 23andMe was ordered by US authorities to stop selling its DNA test kits, a revamped product has gained market approval, the company said.
The California-based firm announced the launch of its new “Personal Genome Service,” which will test for mutations that could lead to disease.
“We’ve worked with the FDA (Food and Drug Administration) for nearly two years to establish a regulatory path for direct-to-consumer genetic testing,” said a statement by 23andMe co-founder and CEO Anne Wojcicki, ex-wife of Google co-founder Sergey Brin.
“We are a better company with a better product as a result.”
The new product is a “complete redesign,” offering “an entirely new experience,” for $199, said the statement from the company, which is named after the 23 pairs of chromosomes in the human body.
Customers will get “a detailed but easy to understand genetic information service,” along with ancestry and wellness reports.
The company also promised “personalized insights based on analysis of 650,000 genetic variations,” and the “only service available direct-to-consumer with reports that meet FDA standards.”
It also mentioned “the chance to find and connect with DNA relatives in a database of more than one million customers.”
The FDA had barred the company in 2013 from selling its saliva analysis kit aimed at helping customers determine their genetic risks for diseases such as diabetes, coronary heart disease and breast cancer, saying it was a “medical device” which required regulatory approval.
– New overhaul –
Medical experts said the company’s test has been completely overhauled, including no longer offering risk analysis on major illnesses such as heart disease, breast cancer and Alzheimer’s.
“The company is not testing the diseases that raised most concerns in the past,” said Cecile Janssens, professor of epidemiology at Emory University, who described the new product as “substantially improved” in terms of information provided.
“It does not test predisposition to common diseases such as heart attack, asthma and hip fractures, for which lifestyle factors are often more important; it does not test high risk variants such as BRCA1 and BRCA2 for breast and ovarian cancer and APOE for Alzheimer’s.”
Instead, the test looks for carrier mutations, or specific gene changes, known to cause health issues when children receive the mutations from both parents.
“The tests are not intended to diagnose a disease, or tell you anything about your risk for developing a disease in the future,” said a company statement.
Rather, the information should mainly be used to learn how DNA relates to these traits, it said.
“Tests for carrier mutations have existed for years and have been available through doctors’ offices, especially for future parents who were concerned about the possibility of hereditary disease,” said Brian Zikmund-Fisher, associate professor of health behavior at the University of Michigan.
“One concern about informing people that they have these types of carrier mutations is that people may not know how to process the information without help.”
Consumers should also be aware that their genetic data may be shared, according to Dietrich Stephan, chairman and professor of the department of human genetics at the University of Pittsburgh Medical Center.
“Their genetic data and their self-reported survey data are being pushed to internal pharmaceutical development and may be shared with external pharmaceutical partners outside of 23andMe,” he added.
“It’s legal and above board, but important for consumers to be aware of.”
– AFP News