A systematic framework for selecting gene-condition pairs for inclusion in newborn sequencing panels: Early Check implementation.

Early Check clinical actionability genome sequencing newborn screening newborn sequencing

Journal

Genetics in medicine : official journal of the American College of Medical Genetics
ISSN: 1530-0366
Titre abrégé: Genet Med
Pays: United States
ID NLM: 9815831

Informations de publication

Date de publication:
04 Oct 2024
Historique:
received: 13 05 2024
revised: 27 09 2024
accepted: 27 09 2024
medline: 8 10 2024
pubmed: 8 10 2024
entrez: 8 10 2024
Statut: aheadofprint

Résumé

Research is underway worldwide to investigate the feasibility, acceptability, and utility of sequencing-based newborn screening. Different methods have been used to select gene-condition pairs for screening, leading to highly inconsistent gene lists across studies. Early Check developed and utilized actionability-based frameworks for evaluating gene-condition pairs for inclusion in newborn panels (Panel 1 - high actionability, Panel 2 - possible actionability). A previously developed framework, the Age-based Semi Quantitative Metric (ASQM), was adapted. Increasing ASQM scores, with a maximum of 15, suggest greater actionability. Wilcoxon tests were performed to compare Panel 1 gene-condition pairs on the Recommended Uniform Screening Panel (RUSP) to non-RUSP pairs. In our first round of assessment, Early Check identified 178 gene-condition pairs for inclusion in Panel 1 and 29 for Panel 2. Median ASQM scores of RUSP conditions on Panel 1 was 12 (range 4 to 15) and non-RUSP was 13 (range 9 to 15). Median scores for Panel 2 was 10 (range 6 to 14). The Early Check frameworks provide a transparent, semiquantitative, and reproducible methodology for selecting gene-condition pairs for NBS sequencing pilot studies that may inform future integration of genomic sequencing into population-level NBS. Collaborative efforts among newborn sequencing studies to establish shared criteria is needed to enhance cross-study comparisons.

Identifiants

pubmed: 39375994
pii: S1098-3600(24)00224-7
doi: 10.1016/j.gim.2024.101290
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

101290

Informations de copyright

Copyright © 2024. Published by Elsevier Inc.

Auteurs

Heidi L Cope (HL)

GenOmics and Translational Research Center, RTI International, Research Triangle Park, North Carolina, USA. Electronic address: hcope@rti.org.

Laura V Milko (LV)

Department of Genetics, The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.

Elizabeth R Jalazo (ER)

Department of Genetics, The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA; Department of Pediatrics, The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.

Blythe G Crissman (BG)

GenOmics and Translational Research Center, RTI International, Research Triangle Park, North Carolina, USA.

Ann Katherine M Foreman (AKM)

Department of Genetics, The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.

Bradford C Powell (BC)

Department of Genetics, The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.

Neal A deJong (NA)

Department of Pediatrics, The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.

Jessica Ezzell Hunter (JE)

GenOmics and Translational Research Center, RTI International, Research Triangle Park, North Carolina, USA.

Beth Lincoln Boyea (BL)

GenOmics and Translational Research Center, RTI International, Research Triangle Park, North Carolina, USA.

Ana N Forsythe (AN)

GenOmics and Translational Research Center, RTI International, Research Triangle Park, North Carolina, USA.

Anne C Wheeler (AC)

GenOmics and Translational Research Center, RTI International, Research Triangle Park, North Carolina, USA.

Rebekah S Zimmerman (RS)

GeneDx, LLC, Gaithersburg, Maryland, USA.

Sharon F Suchy (SF)

GeneDx, LLC, Gaithersburg, Maryland, USA.

Amber Begtrup (A)

GeneDx, LLC, Gaithersburg, Maryland, USA.

Katherine G Langley (KG)

GeneDx, LLC, Gaithersburg, Maryland, USA.

Kristin G Monaghan (KG)

GeneDx, LLC, Gaithersburg, Maryland, USA.

Christina Kraczkowski (C)

GeneDx, LLC, Gaithersburg, Maryland, USA.

Kathleen S Hruska (KS)

GeneDx, LLC, Gaithersburg, Maryland, USA.

Paul Kruszka (P)

GeneDx, LLC, Gaithersburg, Maryland, USA.

Katerina S Kucera (KS)

GenOmics and Translational Research Center, RTI International, Research Triangle Park, North Carolina, USA.

Jonathan S Berg (JS)

Department of Genetics, The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.

Cynthia M Powell (CM)

Department of Genetics, The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA; Department of Pediatrics, The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.

Holly L Peay (HL)

GenOmics and Translational Research Center, RTI International, Research Triangle Park, North Carolina, USA.

Classifications MeSH