Newborn screening for disorders of fatty-acid oxidation: experience and recommendations from an expert meeting

Martin Lindner1, Georg F Hoffmann, Dietrich Matern

  • 1University Children's Hospital, Heidelberg, Germany. Martin.lindner@med.uni-heidelberg.de

Insights

New-born screening (NBS) for fatty-acid oxidation disorders (FAOD) shows a combined incidence of approximately 1:9,300. Expanding NBS programs to include all FAOD, particularly with tandem mass spectrometry, is recommended if laboratory performance is ensured.

Area of Science:

  • Biochemistry
  • Genetics
  • Public Health

Background:

  • New-born screening (NBS) for fatty-acid oxidation disorders (FAOD) is expanding globally.
  • FAOD spectrum and incidence vary significantly across ethnic groups.
  • Current NBS programs demonstrate clear benefits for medium-chain acyl-CoA dehydrogenase deficiency (MCAD) in Caucasian populations.

Framework:

  • International collaboration is crucial for evaluating long-term benefits of NBS for rare FAOD.
  • Standardized confirmatory diagnostic procedures are needed for international data comparability.
  • The inclusion of conditions with uncertain clinical significance, like short-chain acyl-CoA dehydrogenase deficiency (SCAD), can yield valuable knowledge.

Implementation:

  • Tandem mass spectrometry (MS/MS) is a key technology for FAOD screening.
  • High laboratory performance standards are essential for reliable NBS results.
  • Ethnic variations in FAOD prevalence necessitate tailored screening approaches.

Implications:

  • Expanding NBS to include all FAOD is supported by accumulated evidence.
  • MS/MS-based NBS programs offer a viable strategy for comprehensive FAOD detection.
  • Further research and international cooperation are vital for optimizing FAOD screening protocols and understanding disease impact.

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