Collaborative evaluation study on 18 candidate diseases for newborn screening in 1.77 million samples

Abstract: Analytical and therapeutic innovations led to a continuous but variable extension of newborn screening (NBS) programmes worldwide. Every extension requires a careful evaluation of feasibility, diagnostic (process) quality and possible health benefits to balance benefits and limitations. The aim of this study was to evaluate the suitability of 18 candidate diseases for inclusion in NBS programmes. Utilising tandem mass spectrometry as well as establishing specific diagnostic pathways with second-tier analyses, three German NBS centres designed and conducted an evaluation study for 18 candidate diseases, all of them inherited metabolic diseases. In total, 1 777 264 NBS samples were analysed. Overall, 441 positive NBS results were reported resulting in 68 confirmed diagnoses, 373 false-positive cases and an estimated cumulative prevalence of approximately 1 in 26 000 newborns. The positive predictive value ranged from 0.07 (carnitine transporter defect) to 0.67 (HMG-CoA lyase deficiency). Three individuals were missed and 14 individuals (21%) developed symptoms before the positive NBS results were reported. The majority of tested candidate diseases were found to be suitable for inclusion in NBS programmes, while multiple acyl-CoA dehydrogenase deficiency, isolated methylmalonic acidurias, propionic acidemia and malonyl-CoA decarboxylase deficiency showed some and carnitine transporter defect significant limitations. Evaluation studies are an important tool to assess the potential benefits and limitations of expanding NBS programmes to new diseases

Standort
Deutsche Nationalbibliothek Frankfurt am Main
Umfang
Online-Ressource
Sprache
Englisch
Anmerkungen
Journal of inherited metabolic disease. - 46, 6 (2023) , 1043-1062, ISSN: 1573-2665

Ereignis
Veröffentlichung
(wo)
Freiburg
(wer)
Universität
(wann)
2023
Urheber
Maier, Esther M.
Mütze, Ulrike
Janzen, Nils
Steuerwald, Ulrike
Nennstiel-Ratzel, Uta
Odenwald, Birgit
Schuhmann, Elfriede
Lotz-Havla, Amelie Sophia
Weiss, Katharina J.
Hammersen, Johanna
Weigel, Corina
Thimm, Eva
Grünert, Sarah
Hennermann, Julia B.
Freisinger, Peter
Krämer, Johannes
Das, Anibh Martin
Illsinger, Sabine
Gramer, Gwendolyn
Fang-Hoffmann, Junmin
Garbade, Sven
Okun, Jürgen G.
Hoffmann, Georg F.
Kölker, Stefan
Röschinger, Wulf

DOI
10.1002/jimd.12671
URN
urn:nbn:de:bsz:25-freidok-2388851
Rechteinformation
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Letzte Aktualisierung
25.03.2025, 13:54 MEZ

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  • 2023

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