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Time is muscle: A recommendation for early treatment for preterm infants with spinal muscular atrophy
Bo Hoon Lee1,2, Megan A Waldrop3,4, Anne M Connolly3,4
1Child Neurology Division, Department of Neurology, University of Rochester, Rochester, New York, USA.
Insights
Newborn screening increases early spinal muscular atrophy (SMA) diagnosis. We recommend treating preterm infants with SMA at 37 weeks gestational age, aligning with standard definitions for term birth.
Area of Science:
- Genetics and Newborn Screening
- Neuromuscular Disorders
- Pediatric Medicine
Background:
- Newborn screening for spinal muscular atrophy (SMA) is expanding in the US.
- Early diagnosis and treatment are crucial for infants with SMA, particularly those with two to four copies of the survival motor neuron 2 gene.
- Current treatment guidelines lack specific recommendations for preterm infants with SMA.
Abstract:
Implementation of newborn screening for spinal muscular atrophy (SMA) in 33 US states and increased genetic carrier screening have led to an increase in early, presymptomatic diagnosis of SMA. Early treatment is critically important and is recommended for presymptomatic infants with two to four copies of survival motor neuron 2. Currently, no specific treatment recommendations exist for preterm infants with SMA. The US Food and Drug Administration does not recommend using onasemnogene abeparvovec-xioi in preterm infants. Some insurance companies interpret "preterm" to be less than 40 weeks gestational age (GA) instead of the commonly accepted 37 weeks GA, which can be a barrier to treatment access. Given the risk of rapid decline in some infants, we recommend treatment of preterm infants when they reach 37 weeks GA, based on the definitions of term GA from the World Health Organization and Centers for Disease Control and Prevention, assuming all other treatment criteria are met.
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