Newborn Screening by DNA-First: Systematic Evaluation of the Eligibility of Inherited Metabolic Disorders Based on Treatability

Неонатальный скрининг по принципу «сначала ДНК»: систематическая оценка пригодности наследственных метаболических заболеваний на основе их поддаваемости лечению
Abigail Veldman, Birgit Sikkema‐Raddatz, Terry G. J. Derks, Clara D.M. van Karnebeek, Mensiena B. G. Kiewiet, Margaretha F. Mulder, Marcel Nelen, M. Estela Rubio‐Gozalbo, Richard J. Sinke, Monique G. de Sain-van der Velden, Gepke Visser, Maaike C. de Vries, Dineke Westra, Monique Williams, Ron A. Wevers, M. Rebecca Heiner‐Fokkema, Francjan J. van Spronsen
2024-12-28

DNA-first newborn screeningfatty acid oxidationinherited metabolic disordersnext-generation sequencingtreatability criteria
The biomarker-based Dutch Newborn Screening (NBS) panel (as of 2024) comprises 19 inherited metabolic disorders (IMDs). With the use of next-generation sequencing (NGS) as a first-tier screen, NBS could expand to include IMDs that lack a reliable biochemical footprint in dried blood spots, while also reducing secondary findings. To be eligible for inclusion in NBS, an IMD needs to fulfill the Wilson and Jungner criteria, with treatability being one of the most important criteria. In this study, we aimed to identify IMDs eligible for DNA-first NBS when considering only treatability in the context of NBS as a prerequisite. First, three independent reviewers performed a systematic literature review of the 1459 genotypic IMDs and their causative gene(s), as described in the International Classification of Inherited Metabolic Disorders (dated 1 February 2021), applying 16 criteria to exclude non-treatable disorders. Eligible disorders were then discussed in three online meetings with a project group of clinical laboratory geneticists, medical laboratory specialists specialized in IMD, and pediatricians with expertise in IMDs. Based on treatability, we identified 100 genes, causing 95 IMDs, as eligible for NBS, including 42 causal genes for the IMDs in the current biomarker-based NBS. The other 58 genes are primarily associated with treatable defects in amino acid metabolism and fatty acid oxidation. Other IMDs were excluded, most often because of insufficient literature. As the evaluation of treatability was not straightforward, we recommend the development of standardized treatability scores for the inclusion of IMDs in NBS.
1
A systematic evaluation identified 100 genes causing 95 inherited metabolic disorders as potentially eligible for DNA-first newborn screening based on treatability.
2
The additional 58 eligible genes are primarily associated with treatable amino acid metabolism and fatty acid oxidation disorders lacking reliable biochemical screening markers.
3
The eligible disorders include 42 causal genes already represented in the current Dutch biomarker-based newborn screening panel.
4
Three independent reviewers applied 16 exclusion criteria to 1,459 genotypic inherited metabolic disorders, followed by expert-group discussion of eligibility.
5
Treatability assessments were often challenging, and the authors recommend standardized treatability scores to guide inherited metabolic disorder inclusion in newborn screening.

Inherited metabolic disorders (IMDs) considered for DNA-first newborn screening

Eligibility of IMDs for newborn screening based on their treatability

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2024-12-28
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Authors
Abigail Veldman
Birgit Sikkema‐Raddatz
Terry G. J. Derks
Clara D.M. van Karnebeek
Mensiena B. G. Kiewiet
Margaretha F. Mulder
Marcel Nelen
M. Estela Rubio‐Gozalbo
Richard J. Sinke
Monique G. de Sain-van der Velden
Gepke Visser
Maaike C. de Vries
Dineke Westra
Monique Williams
Ron A. Wevers
M. Rebecca Heiner‐Fokkema
Francjan J. van Spronsen
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