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FDA cracks down on company marketing 'three-parent' babies

By Ariana Eunjung Cha

August 8, 2017 at 8:40 AM

(iStock)

Is the Food and Drug Administration moving to assert more control over the genetic manipulation of embryos being used by the reproductive health industry?

On Friday, regulators issued a sternly worded letter to fertility doctor John Zhang, who helped a mother with a genetic disorder give birth to a healthy baby boy by using a procedure that combines DNA from her, her husband and an egg donor. The embryo was created in New York, where Zhang's company is based, and was taken to Mexico, where it was implanted in the mother.

The FDA says that's not allowed. Since 2015, Congress has forbidden the FDA from accepting submissions for clinical investigations that involve intentionally creating a human embryo with a heritable genetic modification. But Zhang's research does just this.

The letter notes that Zhang — who is chief executive of a clinic called New Hope Fertility Center and a research company called Darwin Life — had already agreed not to create any more “three-parent” embryos in the United States, but the letter takes issue with the company's continued marketing of the service. On websites, the companies say the technology will “prevent maternally transmitted diseases” and help prolong “natural fertility.”

“Other applications,” they note, “will be discussed in the future.”

While the technology was originally used to avoid a disease passed through mitochondria, organelles that are passed down through the egg cell, Zhang's clinic was hoping to use it for another purpose — to help women of advanced maternal age who had been unable to conceive in other ways. By using an egg from a younger donor combined with their own DNA, the women would theoretically be able to have their own genetic offspring.

The controversial birth of the first “three-parent” baby was revealed in September 2016, and the science was described in more detail in an article in Reproductive Biomedicine Online in January 2017.

It's unclear why the FDA is weighing in now, almost a year after the experiment became public, although the Trump administration has taken a more conservative approach to reproductive health issues than previous administrations.

The FDA and other government agencies have become more aggressive over the past few years in asserting their powers over emerging industries, but the extent to which their mandates, which were written decades before these technologies were imagined, give them control has been hotly debated. The FDA has been recently working with liquid biopsy companies that aim to detect early signs of cancer in blood and with personal genomic testing companies to ensure they are able to deliver on the marketing promises they are making to consumers.

The United States remains among the most loosely regulated countries when it comes to sperm and egg donation and in vitro fertilization, and there aren't a lot of signs that will change anytime soon. The FDA letter deals with only one company and technology — mitochondrial replacement technology, or MRT — that can be used to form a genetically modified embryo, but things are moving so quickly in the reproductive sciences that experts say it's difficult to predict where we are headed.

Just last week, a team of researchers from Oregon Health & Science University and elsewhere reported that they had “corrected” the DNA of human embryos to erase a heritable heart condition that is known to cause sudden death in young competitive athletes. The FDA hasn't commented on that breakthrough.

This post has been updated.

Read more:

First human embryo editing experiment in U.S. ‘corrects’ gene for heart condition

Sperm concentration has declined 50 percent in 40 years in three continents

There’s a new sheriff in town in Silicon Valley — the FDA


Ariana Eunjung Cha is a national reporter. She has previously served as the Post's bureau chief in Shanghai and San Francisco, and as a correspondent in Baghdad.

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