Psychological Impact of Newborn Screening for 3-Methylcrotonyl-CoA Carboxylase Deficiency: The Parental Experience

Vincenza Gragnaniello1, Giacomo Gaiga1, Chiara Cazzorla1

  • 1Division of Inherited Metabolic Diseases, Department of Women's and Children's Health, University Hospital of Padua, 35128 Padua, Italy.

Insights

Newborn screening for 3-Methylcrotonyl-CoA carboxylase deficiency (3-MCCD) identifies affected infants early. Despite initial parental stress, long-term benefits like avoiding metabolic decompensation outweigh drawbacks.

Area of Science:

  • Metabolic Disorders
  • Newborn Screening
  • Genetics

Background:

  • 3-Methylcrotonyl-CoA carboxylase deficiency (3-MCCD) presents a variable clinical spectrum.
  • Expanded newborn screening has identified many asymptomatic 3-MCCD cases, sparking debate on panel inclusion.

Purpose of the Study:

  • To evaluate long-term outcomes of newborns with positive 3-MCCD screening results.
  • To assess the psychological impact on parents of children with 3-MCCD.

Main Methods:

  • Analysis of 336,668 newborns screened between 2014-2025.
  • Annual clinical and biochemical assessments (acylcarnitine profile, carnitine, urinary organic acids).
  • Parental psychological impact survey and emergency protocol for affected children.

Main Results:

  • Nine infants confirmed with 3-MCCD; one experienced treated metabolic decompensation.
  • One patient showed growth retardation, another transient psychomotor delay; five developed carnitine deficiency.
  • Initial parental psychological impact decreased over time; all parents supported screening.

Conclusions:

  • Newborn screening for 3-MCCD enables early identification and management, preventing severe decompensation.
  • Long-term benefits of 3-MCCD newborn screening outweigh initial parental psychological burden.
  • Screening is beneficial for managing 3-MCCD and its associated health risks.

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