October 4, 2012 in Health, Nation/World

Quicker gene test may help babies

Lauran Neergaard Associated Press
 

WASHINGTON – Too often, newborns die of genetic diseases before doctors even know what’s to blame. Now scientists have found a way to decode those babies’ DNA in just days instead of weeks, moving gene-mapping closer to routine medical care.

The idea: Combine faster gene-analyzing machinery with new computer software that, at the push of a few buttons, uses a baby’s symptoms to zero in on the most suspicious mutations. The hope would be to start treatment earlier, or avoid futile care for lethal illnesses.

Wednesday’s study is a tentative first step: Researchers at Children’s Mercy Hospital in Kansas City, Mo., mapped the DNA of just five children, and the study wasn’t done in time to help most of them.

But the hospital finds the results promising enough that by year’s end, it plans to begin routine gene-mapping in its neonatal intensive care unit – and may offer testing for babies elsewhere, too – while further studies continue, said Dr. Stephen Kingsmore, director of the pediatric genome center at Children’s Mercy.

“For the first time, we can actually deliver genome information in time to make a difference,” predicted Kingsmore, whose team reported the method in the journal Science Translational Medicine.

Even if the diagnosis is a lethal disease, “the family will at least have an answer. They won’t have false hope,” he added.

More than 20 percent of infant deaths are due to a birth defect or genetic diseases, the kind caused by a problem with a single gene. While there are thousands of such diseases – from Tay-Sachs to the lesser known Pompe disease, standard newborn screening tests detect only a few of them. And once a baby shows symptoms, fast diagnosis becomes crucial.

Sequencing whole genomes – all of a person’s DNA – can help when it’s not clear what gene to suspect. But so far it has been used mainly for research, in part because it takes four to six weeks to complete and is expensive.

Wednesday, researchers reported that the new process for whole-genome sequencing can take just 50 hours – half that time to perform the decoding from a drop of the baby’s blood, and the rest to analyze which of the DNA variations uncovered can explain the child’s condition.

Specialists not involved with the study said it signals the long-promised usefulness of gene-mapping to real-world medicine finally is close.

“Genomic sequencing like this is very practical and very real now,” said Dr. Arthur Beaudet of the Baylor College of Medicine. “Fast forward a year, and I think this kind of thing will probably be pretty routine.”

Kingsmore said the speedy test should cost $13,500, and more study is needed for insurers to cover it. But keeping a newborn in ICU costs $8,000 a day, and one question is if the rapid gene-mapping could shorten those stays or avoid futile care, he said.

Among the babies tested was one born with his organs on the wrong side of his body and needing emergency heart surgery. His parents had been told that it was a fluke that his older brother was born the same way, but the new test found an inherited genetic culprit that Kingsmore said will help doctors predict both boys’ future treatment needs.

Three other newborns in the study died, and the new test uncovered the cause of death for two of them. Kingsmore said that allowed researchers to tell parents that nothing they did during pregnancy was to blame, and to counsel them about the risks of future pregnancies.

After the study concluded, the team has performed rapid gene-mapping with additional families. It uncovered the cause of a mother’s two stillbirths, allowing for assisted reproduction to help her next pregnancy be healthy, said Children’s Mercy laboratory director Dr. Carol Saunders.

Another study of genetic diagnosis, also published Wednesday, shows that analyzing more than 21,000 genes can find the cause of unexplained cases of severe mental disability.

Researchers reported in the New England Journal of Medicine that in 16 of 100 patients they were able to identify genetic mutations that caused the condition. The mutations were not inherited from parents but rather occurred spontaneously in the egg or sperm.

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