A Review of Newborn Screening for VLCADD: The Wisconsin Experience
Breanna Mitchell, Jessica Scott-Schwoerer, Ashley Kuhl, Kristina Garcia, Patrice Held

TL;DR
This paper reviews Wisconsin's experience with newborn screening for VLCADD, highlighting improvements in detection accuracy over time.
Contribution
The study identifies specific acylcarnitine markers that improve the accuracy of VLCADD screening.
Findings
Updating the screening algorithm reduced false positives from 25.3% to 20.4%.
The use of C14:1, C14:1/C16, and C14:1/C2 markers showed significant differences between true and false positives.
The positive predictive value decreased due to more carriers being identified.
Abstract
Very-long-chain acyl-CoA dehydrogenase deficiency (VLCADD) is due to a defect in metabolism of long-chain fatty acids. Infants with VLCADD may experience cardiomyopathy, hypoglycemia, or even death; thus, early detection and intervention is crucial. The spectrum of disease and natural variation in newborn metabolism, however, lead to overlap in acylcarnitine values between affected and unaffected individuals, which contributes to the difficulty in identifying true positive cases while minimizing false positive cases. VLCADD was added to the state of Wisconsin’s newborn screening (NBS) panel in 2000. A previous retrospective review of VLCADD screen positive cases identified between 2000 and 2014 resulted in a change to the screening algorithm. Following implementation, a reduction in the percentage of false positive screens from 25.3% to 20.4% was observed between 2015 and 2021. The…
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Taxonomy
TopicsMetabolism and Genetic Disorders · Neonatal Health and Biochemistry · Diet and metabolism studies
