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People who volunteer to participate in medical research usually expect to remain anonymous. That includes those who donate DNA for use in genetic studies. But now, researchers have shown that, in some cases, they can trace a research subject's DNA back to them.
NPR's Veronique LaCapra reports that with more and more personal information available online, the risk of being identified from our genetic information will only increase.
VERONIQUE LACAPRA, BYLINE: An international team of scientists wondered how easy it would be to identify people whose DNA had been posted anonymously on the Internet. They decided to focus on 10 men whose genetic blueprints had been made public for research purposes. By plugging a bit of the men's genetic information into an online service that helps people trace their family histories, they got back a list of possible relatives.
With that list, and information about the age and home state of the men, Yaniv Erlich, of the Whitehead Institute, says his team identified five of them.
YANIV ERLICH: We could actually identify all the other people in the family, basically by looking at public websites, looking at public records of these people, at Facebook and other websites, and be able to connect and to identify all the other people.
LACAPRA: They were able to identify about 50 people in all. Erlich says his study raises big questions about whether it's possible to protect the anonymity of genetic information.
ERLICH: Now, I don't say that everyone now can do this type of study, but it suggests that there is a privacy issue that can be exploited.
LACAPRA: And he's not the only one worried about genetic privacy. Jim Evans, who's a medical geneticist at the University of North Carolina at Chapel Hill, says right now, the risk of privacy violations is relatively low. But he says it's only going to get worse.
JIM EVANS: We can't put the genie back in the bottle. Privacy has been continually eroded in the digital universe in which we live. That's just a fact of life.
LACAPRA: Evans says there needs to be a balance between making genetic data available to researchers and protecting people's privacy. For him, that means limiting who can access genetic information.
EVANS: We need clear policies for how data are handled, with whom they're shared, and importantly, there need to be penalties for violating those policies.
LACAPRA: The fear is that people who volunteer to provide their DNA for research may be vulnerable to genetic discrimination. But even with the risks, some people are OK with putting their genetic data out there for everyone to see.
Harvard Medical School genetics professor George Church runs a genetic database that anybody, not just scientists, can access. People who want their DNA in the database are told about the possible privacy risks up front. Church says, even so, many people still want to participate.
GEORGE CHURCH: I think people are more trusting if you're open and transparent with them about what the risks are.
LACAPRA: In their paper published today in the journal Science, Yaniv Erlich and his colleagues don't reveal the names of the people they identified or the details of how they did it. But they did contact the National Institutes of Health. That's the agency that funded project that posted the genetic information online in the first place.
The NIH's Laura Lyman Rodriguez says most genetic data is more tightly protected. But she acknowledges the new study shows that the privacy of research subjects can't be guaranteed.
LAURA LYMAN RODRIQUEZ: And what we really think needs to happen at this point in time, now that this threshold has been reached where individuals have been identified through the connection of research and non-research information, is to have a public dialogue.
LACAPRA: A public dialogue about how best to protect privacy without inhibiting research. In the meantime, the NIH has removed some details about the people whose genetic data is on the Internet, in an effort to keep a similar privacy breach from happening again.
Veronique LaCapra, NPR News.
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