Beyond newborn screening: the role of reverse cascade testing in familial disease detection

Amy Gaviglio1, Kostantinos Petritis2, Veronica Tagi3

  • 14ES Corporation, Contractor, Newborn Screening and Molecular Biology Branch, Division of Laboratory Sciences, National Center for Environmental Health, Centers for Disease Control and Prevention, Atlanta, GA, USA.

Insights

Newborn screening (NBS) can identify rare inherited diseases, enabling family-wide prevention through reverse cascade testing (RCS). This strategy assesses conditions for RCS suitability, benefiting affected families and potentially identifying maternal risks.

Area of Science:

  • Genetics
  • Public Health
  • Pediatrics

Background:

  • Newborn screening (NBS) has evolved to detect rare congenital inherited diseases.
  • Many NBS conditions are autosomal recessive or X-linked, posing risks to family members.
  • NBS can serve as a crucial entry point for family-wide preventative strategies like reverse cascade testing (RCS).

Purpose of the Study:

  • To examine scenarios where reverse cascade testing (RCS) is appropriate within newborn screening (NBS).
  • To establish criteria for identifying NBS diseases that would benefit from RCS.
  • To highlight potential benefits of RCS for specific inherited disorders and maternal conditions detected through NBS.

Main Methods:

  • Developed criteria to assess RCS appropriateness for NBS diseases: inheritance pattern, carrier rates, expressivity, onset, and diagnostic delays.
  • Applied criteria to identify diseases like X-linked adrenoleukodystrophy (X-ALD), Cystic Fibrosis, Sickle Cell Disease, Spinal Muscular Atrophy, and Pompe disease.
  • Considered maternal conditions (e.g., vitamin B12 deficiency) as indicators for RCS in NBS.

Main Results:

  • Identified key criteria for determining RCS suitability in NBS programs.
  • Highlighted specific inherited diseases (X-ALD, CF, SCD, SMA, Pompe) where RCS offers significant benefits.
  • Demonstrated the value of RCS in cases of maternal nutritional deficiencies, preventing potential newborn complications and maternal health risks.

Conclusions:

  • RCS is a valuable strategy for family-wide prevention initiated through NBS.
  • A defined set of criteria can guide the implementation of RCS for NBS-detected conditions.
  • Successful RCS implementation requires careful consideration of educational, ethical, logistical, and clinical management aspects.