NEW YORK (AP) - Imagine being pregnant and taking a simple blood test that lays bare the DNA of your fetus. And suppose that DNA could reveal not only medical conditions like Down syndrome, but also things like eye color and height. And the risk for developing depression or Alzheimer’s disease. And the chances of being gay.
So far that’s still science fiction. But scientists have been taking some baby steps in that direction. And some ethics experts say it’s time to start talking now about what that could mean for parents and society.
This is the second story in a two-part series on fetal DNA testing and the ethical issues raised by it.
Scanning fetal DNA from a blood test will be “without question a major medical advance that promises to greatly improve current prenatal care,” says Jaime King, an associate professor at the UC Hastings College of Law in San Francisco who studies genetic testing. But bringing it into practice “raises significant practical, legal, ethical and social challenges,” she says.
“This really changes the experience of what it will be like to be pregnant and have a child,” said Marcy Darnovsky of the Center for Genetics and Society in Berkeley, Calif. “I keep coming up with the word, game-changer.”
She wonders if parents would withhold their commitment to a pregnancy until test results show a fetus is “good enough” to be born. And what, she asks, is good enough?
She and others worry about how well couples will be able to understand this flood of information, and just what should be revealed.
The issues have been discussed before. The DNA of a fetus has long been recoverable through medical procedures, with a small risk of miscarriage. But a blood test would be free of that risk, which should make many more women interested in it and doctors willing to test for a wider range of conditions, some experts say. And the results could come early enough to allow for an abortion before the pregnancy is even obvious.
The trigger for the new round of discussion is a couple of papers published last December. In preliminary results, two research teams showed that they could essentially reconstruct a baby’s genetic makeup by recovering fragments of fetal DNA from the mother’s bloodstream. That ability, plus the rapidly falling cost of analyzing DNA, would open the door to inspecting individual genes.
That would go well beyond the more accurate prenatal blood test for Down syndrome that some companies hope to market within a year.
Within five to 10 years, doctors may be able to test for 100 or 200 diseases, albeit many of them rare, estimates Stanford University law professor Hank Greely, who studies the implications of biomedical technologies.
Prenatal testing “is going to put a lot more information about the genetics of a child into the hands of a lot more parents,” said King.
That knowledge has a flip side. “How much responsibility are we expecting people to take for the genetic makeup of any child they might have?” asks Josephine Johnston, a research scholar at the Hastings Center, a bioethics think tank near New York City.View Entire Story
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