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The results are not so different from some studies involving genetic testing for other conditions, like Huntington's disease or some types of cancer, said Elizabeth Thomson, an official at the National Human Genome Research Institute.
"It seems to be worse on people not to know than to know that they are positive or negative," said Thomson, director of the federal agency's ethical, legal and social implications research program.
Indeed, in the Alzheimer's study, 16 percent of those in the group that did not get results dropped out -- a higher proportion than those who left the other group. That may have been a sign of frustration of people who really wanted the information, said Green.
"Once you make up your mind that this is something you're interested in learning, you really don't want to be told no," Green said. It's possible that stress levels were elevated in the people who didn't get the results, he said.
The study was funded by the National Institutes of Health. Two of the authors -- not Green -- last year received consulting fees from Smart Genetics, a Philadelphia company that provided direct-to-consumer genetic testing. The company has since gone out of business.
Testing remains a complicated decision, even for people who know a lot about it. Peshkin, the genetic counselor, said her 80-year-old father has Alzheimer's, but she has decided not to get the test.
"Even though I understand the uncertainty of how predictive the test is, it would be something I'd be very anxious about," said Peshkin, 41. "I would be one of those people that the first moment I couldn't remember someone's name, I'd think 'Oh God, here it comes.' I'd rather not know."
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