Skip to Content

The End for Direct-to-Consumer Genetic Testing?

Updated: An advisory panel for the FDA recommends that some genetic tests require the involvement of health care providers.
March 10, 2011

Updated: 03/11/2011

In a blow to both the consumer genomics industry and advocates of patient-centered healthcare, an advisory panel for the Food and Drug Administration has recommended that some direct-to-consumer genetic tests–kits sold over the internet that give consumers information about their genetic risk for common diseases as well as other genetic information–no longer be freely available to consumers. According to a report from Medpage today, the panel recommended that “Certain types of genetic tests that are available for at-home use without a prescription should not be used without the involvement of a physician or genetic specialist.”

The panel wasn’t clear on whether that would mean a physician would have to order the test, or if a physician would have to interpret the test, or both. That will ultimately be up the FDA to decide. The agency – which may decide to make certain tests that are currently DTC [direct to consumer] available by prescription only – isn’t required to follow the advice of its advisory committees, but it often does.

However, Alberto Gutierrez, director of the FDA’s Office of In Vitro Diagnostics, did point out that different types of tests are likely to be regulated differently.

“We’re not going to be able to take one approach to all types of tests,” Gutierrez said. “Some may not require a doctor at all and some might require that a qualified health professional be involved, and some might involve the doctor to order the test.”

… certain types of tests, such as nutrogenetic tests, might be appropriate for at-home use as long as the companies make truthful claims.

Other tests, such as carrier screening tests – which show whether a person is a genetic carrier of a condition and therefore has a risk of passing it on to their children – may eventually require doctor involvement.

(For more details on the proceedings, see excellent posts by Dan Vorhaus of the Genomics Law Report and Daniel MacArthur of Genomic Future.)

That recommendation, which industry observers expected, has caused an outcry among proponents of direct-to-consumer testing, who say that consumer tests allow people—especially patients suffering from specific diseases—to become participants in their health care, and in research surrounding their disease, rather than merely subjects.

As MacArthur notes; “…this is an obsolete, paternalistic vision for genomic medicine that flies in the face of primary physicians’ self-admitted ignorance of genetics, and will become simply untenable as we enter the era of cheap whole-genome sequencing.”

Early evidence suggests that one of the main concerns over direct-to-consumer genetic testing–that people will react badly to information about disease risk if a physician is not involved–is overblown. A paper published in the New England Journal of Medicine last year found that people who took Navigenics’ test did not make significant changes in their behavior for the better or worse. The study was limited to people who expressed interest in taking the test, and so may not reflect the general public, but it is likely representative of potential customers.

One of the more interesting trends to emerge from consumer genetic testing is patient-driven genetic research, an approach pioneered by 23andMe. As I noted in a blog last year, the company has more than 400 ongoing studies searching for the genomic basis for everything from flu symptoms and asthma to dry mouth after taking the allergy drug zyrtec and euphoria after taking codeine. Following on this theme, Joe Pickrell at Genomes Unzipped highlights why consumer genetic testing is good for research:

You can think what you want about the value of the research done to date by 23andme [1], but in my mind, there’s one simple reason why the sorts of participant-driven research they’re doing can only be a good thing: all research is driven by curiosity, and the people most curious about a disease or trait are those who have it. While people may think of the academic research community as a machine with endless resources and limitless motivation, it’s not. People work on things they think are interesting; they sometimes follow “trendy” topics, or move into fields with more grant money, or get bored of a given problem and move on. So if the research in the trait you’re most interested in isn’t moving fast enough for you, well, tough luck.

Adding to the controversy is a video posted on YouTube by the FDAblog, which questions the validity of statements made to Congress by Jeffrey Shuren, a senior FDA official with the Government Accountability Office. Last year, the GAO presented a damning report on the consumer genomics industry, highlighting deceptive marketing practices.

According to the FDAblog;

“The statement, for 23andMe in particular, that ‘they are not doing their own research on the genetic profiles,’” said Stanford’s Serafim Batzoglou, “is patently false.” “Clearly this is false,” said Russ Altman, also at Stanford. “I am reviewing [23andMe’s paper] in my annual review of translational bioinformatics.”

The House recently moved to demote and discipline Gregory Kutz of the GAO for providing systematically misleading information to Congress. Mr. Kutz and Mr. Shuren testified together in the July 22, 2010 hearing, and the FDA is currently slated to have hundreds of millions cut from its budget by a Republican Congress.

So what now?

Vorhaus says;

Whatever the MCGP’s [Molecular and Clinical Genetics Panel] recommendations, whether for or against DTC genetic testing, my advice will be the same: move on.

Throughout the day the FDA was clear that it was asking the panel for assistance with a fairly narrow set of questions. Not on the table: whether DTC genetic tests will be regulated. They will be, at least for analytical and clinical validity. Exactly what that regulation will look like will be heavily influenced by how the FDA ultimately decides to regulate LDTs [laboratory developed tests]. For purposes of the MCGP’s recommendations, the FDA appears to be interested solely in the narrower question of when, if at all, a genetic test should be offered directly to consumers.

Keep Reading

Most Popular

Russian servicemen take part in a military drills
Russian servicemen take part in a military drills

How a Russian cyberwar in Ukraine could ripple out globally

Soldiers and tanks may care about national borders. Cyber doesn't.

Death and Jeff Bezos
Death and Jeff Bezos

Meet Altos Labs, Silicon Valley’s latest wild bet on living forever

Funders of a deep-pocketed new "rejuvenation" startup are said to include Jeff Bezos and Yuri Milner.

conceptual illustration showing various women's faces being scanned
conceptual illustration showing various women's faces being scanned

A horrifying new AI app swaps women into porn videos with a click

Deepfake researchers have long feared the day this would arrive.

ai learning to multitask concept
ai learning to multitask concept

Meta’s new learning algorithm can teach AI to multi-task

The single technique for teaching neural networks multiple skills is a step towards general-purpose AI.

Stay connected

Illustration by Rose WongIllustration by Rose Wong

Get the latest updates from
MIT Technology Review

Discover special offers, top stories, upcoming events, and more.

Thank you for submitting your email!

Explore more newsletters

It looks like something went wrong.

We’re having trouble saving your preferences. Try refreshing this page and updating them one more time. If you continue to get this message, reach out to us at customer-service@technologyreview.com with a list of newsletters you’d like to receive.