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Verfasst von:Maier, Esther M. [VerfasserIn]   i
 Mütze, Ulrike [VerfasserIn]   i
 Janzen, Nils [VerfasserIn]   i
 Steuerwald, Ulrike [VerfasserIn]   i
 Nennstiel-Ratzel, Uta [VerfasserIn]   i
 Odenwald, Birgit [VerfasserIn]   i
 Schuhmann, Elfriede [VerfasserIn]   i
 Lotz-Havla, Amelie S. [VerfasserIn]   i
 Weiss, Katharina J. [VerfasserIn]   i
 Hammersen, Johanna [VerfasserIn]   i
 Weigel, Corina [VerfasserIn]   i
 Thimm, Eva [VerfasserIn]   i
 Grünert, Sarah [VerfasserIn]   i
 Hennermann, Julia B. [VerfasserIn]   i
 Freisinger, Peter [VerfasserIn]   i
 Krämer, Johannes [VerfasserIn]   i
 Das, Anibh M. [VerfasserIn]   i
 Illsinger, Sabine [VerfasserIn]   i
 Gramer, Gwendolyn [VerfasserIn]   i
 Fang-Hoffmann, Junmin [VerfasserIn]   i
 Garbade, Sven [VerfasserIn]   i
 Okun, Jürgen G. [VerfasserIn]   i
 Hoffmann, Georg F. [VerfasserIn]   i
 Kölker, Stefan [VerfasserIn]   i
 Röschinger, Wulf [VerfasserIn]   i
Titel:Collaborative evaluation study on 18 candidate diseases for newborn screening in 1.77 million samples
Verf.angabe:Esther M. Maier, Ulrike Mütze, Nils Janzen, Ulrike Steuerwald, Uta Nennstiel, Birgit Odenwald, Elfriede Schuhmann, Amelie S. Lotz-Havla, Katharina J. Weiss, Johanna Hammersen, Corina Weigel, Eva Thimm, Sarah C. Grünert, Julia B. Hennermann, Peter Freisinger, Johannes Krämer, Anibh M. Das, Sabine Illsinger, Gwendolyn Gramer, Junmin Fang-Hoffmann, Sven F. Garbade, Jürgen G. Okun, Georg F. Hoffmann, Stefan Kölker, Wulf Röschinger
Jahr:2023
Umfang:20 S.
Fussnoten:Vor der Veröffentlichung im Heft online veröffentlicht: 21. August 2023 ; Gesehen am 20.10.2023
Titel Quelle:Enthalten in: Journal of inherited metabolic disease
Ort Quelle:Hoboken, NJ : Wiley, 1978
Jahr Quelle:2023
Band/Heft Quelle:(2023), Seite 1-20
ISSN Quelle:1573-2665
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.
DOI:doi:10.1002/jimd.12671
URL:Bibliographic entry. University members only receive access to full-texts for open access or licensed publications.

kostenfrei: Volltext: https://doi.org/10.1002/jimd.12671
 kostenfrei: Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/jimd.12671
 DOI: https://doi.org/10.1002/jimd.12671
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:dried blood spot
 evaluation study
 Germany
 inborn errors of metabolism
 newborn screening
 public health
 tandem mass spectrometry
K10plus-PPN:1866657135
Verknüpfungen:→ Journal

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