Orlando Sentinel

Assisted reproducti­on getting assist

Embryos’ DNA could soon be decoded, opening ethical woes

- By Malcolm Ritter

NEW YORK — So you want to have a baby.

Would you like a darkhaired girl with a high risk of someday getting colon cancer, but a good chance of above-average music ability?

Or would you prefer a girl with a good prospect for high SAT scores and a good shot at being athletic, but who also is likely to run an above-average risk of bipolar disorder and lupus as an adult?

How about a boy with a good shot at having musical ability and dodging asthma, but who also would be predispose­d to cataracts and Type 2 diabetes? Confused? That’s just an inkling of the future a biomedical ethics expert envisions for 20 to 40 years from now — soon enough that today’s children may face it when they start their own families.

“The majority of babies of people who have good health coverage will be conceived this way,” predicts Henry Greely, a Stanford University law professor who works in bioethics.

You’ve probably read about concerns over “designer babies,” whose DNA is shaped by gene editing. Greely is focused on a different technology: In a startling bit of biological alchemy, scientists have shown that in mice, they can turn ordinary cells into sperm and eggs.

It’s too soon to know if it could be done in people. But if it can, it could become a powerful infertilit­y treatment, permitting genetic parenthood for people who can’t make their own sperm or eggs.

And that means a lot of choices.

Here’s what Greely envisions: A man and woman walk into a fertility clinic. The man drops off some sperm. The woman leaves some skin cells, which are turned into eggs and fertilized with the man’s sperm.

Unlike in vitro fertilizat­ion today, which typically yields around eight eggs per try, the new method could result in 100 embryos.

The embryos’ complete library of DNA would be decoded and analyzed to reveal genetic predisposi­tions, both for disease and personal traits.

Out of, say, 80 suitable embryos, the couple would then choose one or two to implant.

The technology might also help open the door to same-sex couples having children geneticall­y related to both of them, though the additional twist of making eggs from men or sperm from women would be a huge biological challenge.

Real life is already creeping toward such a future. Some scientists are trying to make human eggs and sperm in the lab.

Amander Clark of the University of California at Los Angeles, says her goal is to aid basic research into why some people are infertile. She acknowledg­es the technique might itself be used to treat some infertilit­y, particular­ly in young people made sterile by cancer treatments.

As for decoding the complete DNA library of embryos, Dr. Louanne Hudgins, who studies prenatal genetic screening and diagnosis at Stanford, says some pregnant patients there say they’ve already had fertility clinics do that. They didn’t reveal why, Hudgins said.

Hudgins, who’s president of the American College of Medical Genetics and Genomics, said no national medical associatio­n has endorsed decoding all the DNA of an embryo, which is called its genome. So she believes no insurance company would pay for that now.

Greely, who lays out his ideas in a book called “The End of Sex and the Future of Human Reproducti­on,” calls his vision “easy PGD,” or prenatal genetic diagnosis.

Ordinary PGD has been done for decades. When a couple is known to be at risk for having a child with a specific genetic disorder, such as cystic fibrosis or sickle cell anemia, the woman undergoes a procedure to remove some eggs. After fertilizat­ion, some cells are plucked from the embryos and examined to identify whether those carry the diseasecau­sing abnormalit­y.

That procedure looks for a specific problem in a few embryos, not entire genomes from dozens of them. If a couple wants to select a “super baby,” says Dr. Richard Scott Jr., a founding partner of Reproducti­ve Medicine Associates of New Jersey, “we tell them we can’t do it.”

Additional­ly, even if DNA is the hardware, there’s also the software: chemical modificati­ons that determine when and where particular genes turn on and off. Much of this “epigenome” would develop after an embryo’s genes are sampled, Scott said.

“Your child may not turn out to be the three-sport All-American at Stanford,” because “the epigenome didn’t work out,” Scott said.

Greely agrees that prediction­s about behavioral traits like intelligen­ce and athletic ability will be imprecise, because of epigenetic­s and because of basic uncertaint­ies about what genes are involved and how they interact. And a person’s upbringing and life experience­s have a big effect.

Even if the prediction­s aren’t perfect, would couples want to take steps to control their child’s genetics? Many experts doubt it.

Only a “very small minority” seek a perfect baby, says Stanford’s Hudgins. In her practice, she said she often finds women pass up all screening because they figure the baby’s fate is “in God’s hands.”

Greely doubts that influencin­g brainpower or athleticis­m would be a major draw for parents. Instead, he thinks they would care most about avoiding awful diseases that strike in infancy or childhood. They’ll probably be less concerned about illnesses that might show up later in life, such as Alzheimer’s or Parkinson’s.

He thinks easy PGD is coming, and it would be better if properly handled. He says it should be proven safe, subsidized, monitored for long-term effects, and regulated so that parents can choose whether to use it and decide what embryonic traits to focus on.

But, once the genetic profile is done, could it come back to haunt a child if, say, a life insurer or nursing home demanded to see it to assess disease risk? How would the large number of rejected embryos be handled ethically and politicall­y?

Perhaps future regulation could limit the number of embryos created, as well as what traits a couple could select for, said I. Glenn Cohen, a Harvard law professor.

Lori Andrews, a professor at the Chicago-Kent College of Law, summed up her views in a review of Greely’s book.

“The idea of easy PGD,” she wrote, “should make us uneasy indeed.”

Still, even some who doubt the idea’s feasibilit­y say Greely is right to raise the issue.

“This is not just a technical or science question,” said Marcy Darnovsky, who writes on the politics of human biotechnol­ogy as executive director of the Center for Genetics and Society in Berkeley, Calif.

 ?? OREGON HEALTH AND SCIENCE UNIVERSITY ?? Human embryos grow in a lab after researcher­s used gene editing technology to repair a heart disease-causing genetic mutation. Burgeoning technology that can turn ordinary cells in mice into sperm and eggs could be just as revolution­ary.
OREGON HEALTH AND SCIENCE UNIVERSITY Human embryos grow in a lab after researcher­s used gene editing technology to repair a heart disease-causing genetic mutation. Burgeoning technology that can turn ordinary cells in mice into sperm and eggs could be just as revolution­ary.

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