THURSDAY, Feb. 21 (HealthDay News) -- New guidelines on testing
newborns and children for genetic diseases recommend screening for
childhood diseases but note that testing for diseases that strike
in adulthood may not be worthwhile.
About 4 million infants in the United States undergo newborn
screening each year, but further genetic testing -- while
increasingly available -- is less common. Newborn screening panels
vary from state to state.
All newborns should be tested for the genetic diseases that are
included in their state's newborn screening panel, but anything
beyond that is up to parents and the decision must be made in the
child's best interest, according to the revised policy statement
from the American Academy of Pediatrics and the American College of
Medical Genetics and Genomics. The new guidelines are published
online Feb. 21 in the journal
The recommendations distinguish between genetic testing for
childhood-onset conditions versus those for adult-onset conditions.
For kids who may be at risk for a childhood disease, testing is
worth considering, the guidelines state, but the same does not hold
true if the child is thought to be at risk for a disease that
strikes in adulthood.
"There is an important role for counseling before and after genetic screening," added policy author Dr. Lainie Friedman Ross, a pediatrician and ethicist at the University of Chicago. "The focus should be on education of families, counseling them and helping them make decisions that focus on the child's best interest."
The new guidelines do not call for any specific genetic tests;
instead they recommend mandatory offering of state newborn
screening panels. "We believe that if parents are informed that the
benefits outweigh the risks, that they will give their permission,
given that all states screen for at least the uniform panel and it
is included in costs of birth hospitalization," Friedman Ross
Testing for disease in the presence of symptoms is another area
addressed by the new recommendations. "Clearly, if a child has
symptoms, we need a diagnosis to help the family make clinical
decisions that are in the child's best interest. This is important
even when the disease has no current therapies," Friedman Ross
Kids should also be informed of the results when they reach an
appropriate age, she added.
The guideline authors caution against using direct-to-consumer
genetic screening tests, because there is no oversight and the
results are open to interpretation.
Pediatricians and geneticists said they are on board with the
"In newborns, we look for things that are treatable and have interventions that will have a significant impact on the child," said Dr. Marshall Summar, division chief of genetics and metabolism at Children's National Medical Center in Washington, D.C.
But "it's a moving target," he said. "We have to constantly
reassess this as the technology and our understanding of what the
results mean changes."
There are risks when it comes to broad-based gene screens
outside of traditional newborn screening panels, said Dr. Parul
Jayakar, a clinical and metabolic geneticist at Miami Children's
Hospital. "We may find things that never come to fruition or
results that we can't fully interpret yet," he explained.
However, there are also cases were being forewarned is being
forearmed, said Dr. Joyce Fox, a medical genetics doctor at North
Shore University Hospital in Manhasset, N.Y.
If there is a family history of a genetic disease, even
adult-onset ones, there are some instances where knowing this early
will make a difference. This includes certain cancers, including a
rare type of inherited colon cancer. "We would want the information
earlier so we can do appropriate surveillance on the children and
prevent the onset of significant disease," Fox said.
But it should be buyer beware when it comes to
direct-to-consumer gene screens, she said.
"We highly discourage these even on adults, and particularly on children, because there is nobody there to provide counseling and interpretation," Fox said. These can also be very costly, and are likely not covered by insurance."
Learn more about newborn screening at the
U.S. National Institutes of Health.
Please be aware that this information is provided to supplement the care provided by your physician. It is neither intended nor implied to be a substitute for professional medical advice. CALL YOUR HEALTHCARE PROVIDER IMMEDIATELY IF YOU THINK YOU MAY HAVE A MEDICAL EMERGENCY. Always seek the advice of your physician or other qualified health provider prior to starting any new treatment or with any questions you may have regarding a medical condition.
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