Summary: Valley Children’s Precision Medicine Program is pioneering a genetic test that quickly identifies infants at risk of aminoglycoside-induced hearing loss, allowing doctors to choose safer antibiotics.
Key Takeaways:
- Rapid Genetic Testing: The test identifies MT-RNR1 gene variants in under an hour, enabling timely, personalized treatment decisions for sick infants.
- Preventing Hearing Loss: Early identification of genetic risk allows doctors to avoid aminoglycosides, preventing potential long-term hearing damage.
- Innovative Care: This approach is part of a broader effort to integrate advanced genetic testing into patient care, improving outcomes for critically ill infants.
What if a gentle swab of an infant’s cheek was all it took to know if giving them a common antibiotic could also lead to long-term hearing loss?
That is what Valley Children’s Precision Medicine Program is doing: the team is the first in the nation to use a revolutionary genetic test that can quickly let a doctor know if their tiny patient is at higher risk of hearing damage from a type of antibiotic known as an aminoglycoside. Once a doctor knows that the baby has a particular version of a key hearing gene, they can then choose a different course of care to treat an infection.
“Genes are like the individual instructions in a book that tell the body how to build and work, so understanding them is important in creating a treatment plan for each patient,” says Jeremy Woods, MD, Valley Children’s geneticist and director of the Precision Medicine Program in Madera, Calif.
Aminoglycosides and Hearing Loss Risk
Aminoglycosides are a class of antibiotics often used to treat infections for infants in the neonatal intensive care unit (NICU). But in addition to attacking bacteria, the medicines can also attack human proteins that are vital to hearing development. That’s not usually a problem, but for babies born with certain variants of the MT-RNR1 gene, the risk for aminoglycoside-induced hearing loss (AIHL) is much greater. Insights suggest that this could be the explanation for at least 1% of hearing loss that occurs in children before language development, and likely more.
The problem until now was being able to check the baby’s genetic “map” quickly if they got sick. Valley Children’s has solved that with a simple, non-invasive test. A small saliva sample from the baby’s cheek is then analyzed by a special machine that tests for changes in the MT-RNR1 gene. The machine is no larger than an inkjet printer and can deliver results to physicians in under an hour when time is of the essence. Valley Children’s Precision Medicine team is conducting MT-RNR1 rapid testing for patients outside of the hospital, with plans to standardize this process for babies in the hospital later this year.
“Previously, we would have to wait weeks for the results of MT-RNR1 genetic testing. Now, we can have results back in under an hour,” Woods says. “That gives us plenty of time to choose a safer antibiotic to treat a seriously ill baby.”
Valley Children’s Precision Medicine Program Innovations
This life-changing advancement is one of several innovative tools pioneered by Valley Children’s Precision Medicine Program. Earlier this year, the hospital began using an advanced genetic testing module as part of the electronic patient information system. This system allows providers to effortlessly order a comprehensive genetic test (whole genome sequencing) that includes one or both parents and provides instant care recommendations based on a child’s specific genetic map.
Valley Children’s was also one of only five institutions to participate in a Medi-Cal pilot program called Project Baby Bear, which used rapid whole genome sequencing to improve the care for critically ill infants with undiagnosed illnesses.
“Standardizing genome testing in the NICU underscores our commitment to utilizing cutting-edge technology and genetics to provide our patients with more than the best care, but the specialized kind of care they need,” Woods says.
