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DNA firms under microscope

Confusion over testing policy persists as California orders several companies to 'cease and desist.'

MEDICINE / A CLOSER LOOK: GENE TESTS

July 14, 2008|Karen Ravn, Special to The Times

The health department has legal options -- seeking injunctions, pursuing criminal prosecutions -- to stop companies from continuing to practice their businesses. It will not comment on its plans. Representatives of Navigenics and 23andMe say they would like to meet with state health officials to discuss the impasse and try to resolve it. "There could be friendly compromise, or it could end up in the courts," Weiss says.


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Do we need new rules and regulations for this new industry?

Greely thinks so. "The current legislation was certainly not written with this industry in mind," he says. Hudson says the main goal of state or federal regulations should be to guarantee that tests are safe and accurate and that claims made about them are truthful. Ideally, federal laws would be written, says Dr. Robert Nussbaum, chief of the Division of Medical Genetics at UC San Francisco: "State by state would be a nightmare." There are no federal laws yet on the matter of direct-to-consumer gene testing.

Still, Weiss cautions that medical regulation has historically been up to the states, and he doubts they'll want to give up control entirely.

health@latimes.com

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Valid or void?

Everyone agrees that the science of gene testing is imperfect, but the companies offering tests directly to consumers, along with their supporters, say the information they give is valid and valuable, noting that clients can get updates as more is learned.

Critics aren't so sure that the people being tested always get their money's worth. And many believe that even when gene tests and claims about links to diseases are accurate, they may be confusing. "This kind of testing, this kind of knowledge about ourselves, is so new," says Dr. Edward McCabe, co-director of the UCLA Center for Society and Genetics. "We can get a whole lot of information, and we're not going to know what a lot of it means."

Some testing companies work hard to solve this problem. For example, Navigenics of Redwood Shores employs three highly trained full-time genetic counselors, one of whom is assigned to each client.

Still, says Dr. Robert Nussbaum, chief of the Division of Medical Genetics at UC San Francisco, no matter how well it's explained, some of the information people get simply doesn't mean much. Some DNA tests are highly predictive of disease -- for example, tests for mutations in the cystic fibrosis gene -- but others are based on flawed data or so weakly predictive that many who test negative will end up getting the disease, while many who test positive will not (an example would be tests for risk of Type 2 diabetes).

In such cases, Nussbaum says, "the information is basically useless." It might even be counterproductive, he adds, if someone who tests negative -- for, say, diabetes risk -- then has less incentive to adopt healthful life habits.

Even highly predictive tests can be unhelpful if they predict conditions that can't be treated or prevented, such as Huntington's disease, Nussbaum adds. They can simply make a client worried or scared.

In all, says Hank Greely, director of the Center for Law and the Biosciences at Stanford University, while some companies clearly provide useful information to their clients, "some companies provide nothing beyond a new way of wasting money."

-- Karen Ravn

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