When infants are admitted into intensive care units (ICUs), physicians and care teams must move quickly to make a diagnosis and begin the best course of treatment. However, in infants suspected to have a genetic disorder, testing can take months, losing valuable time and causing stress to the patient and family. A team of physicians and researchers from Baylor College of Medicine, Texas Children’s Hospital and Baylor Genetics designed a study to determine the efficacy of exome sequencing in intensive care units. The results appear in JAMA Pediatrics.
“In our study we were looking to answer two key questions: can we appropriately diagnose infants with genetic disorders in critical care units using exome sequencing, and will our findings result in changes to their medical care,” said Dr. Seema Lalani, associate professor of molecular and human genetics at Baylor.
“There are times when we see babies who have various problems, but we aren’t sure what the underlying diagnosis is. Through this research, we were hoping to address these diagnostic barriers through whole exome sequencing,” added Dr. Mohan Pammi, associate professor of pediatrics – neonatology at Baylor.
Exome sequencing analyzes a specific part of the genome called the coding region, made up of about 20,000 genes, where the majority of known defects occur.
The research team performed clinical exome sequencing for 278 unrelated infants who were 100 days old or younger. Types of exome sequencing performed included proband, trio and critical trio, the latter of which is a rapid genomic assay for seriously ill infants. Results from critical exome sequencing take about two weeks to complete, which is much faster than many other diagnostic options.
“Infants were selected for exome sequencing based on several characteristics we know to be associated with genetic disorders. Many of them had serious birth defects due to genetic changes that could not be easily diagnosed by clinical exam,” Lalani said.
These characteristics included neuromuscular diseases, syndromic congenital cardiovascular malformations, hypertrophic cardiomyopathy, skeletal malformations, neonatal cholestasis and liver failure, lung disease and metabolic disorders.
Of the 278 infants, a molecular diagnosis was found in 102 cases through clinical exome sequencing. Diagnosis resulted in altered medical management for 53 of these infants by redirecting their care, bringing in a new subspecialist, making dietary changes and even furthering life-saving procedures in some cases.
Sixty-three of the patients received critical trio exome sequencing specifically, resulting in a diagnosis for 32 infants in this group. Of these 32 infants, diagnosis altered clinical care in 23 cases.