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Evaluation of 11 years of newborn screening for maple syrup urine disease in the Netherlands and a systematic review of the literature: Strategies for optimization.
Stroek, Kevin; Boelen, Anita; Bouva, Marelle J; De Sain-van der Velden, Monique; Schielen, Peter C J I; Maase, Rose; Engel, Henk; Jakobs, Bernadette; Kluijtmans, Leo A J; Mulder, Margot F; Rubio-Gozalbo, M E; van Spronsen, Francjan J; Visser, Gepke; de Vries, Maaike C; Williams, Monique; Heijboer, Annemieke C; Kemper, Evelien A; Bosch, Annet M.
Afiliación
  • Stroek K; Endocrinology Laboratory, Department of Clinical Chemistry Amsterdam Gastroenterology & Metabolism, Amsterdam UMC, University of Amsterdam Amsterdam The Netherlands.
  • Boelen A; Endocrinology Laboratory, Department of Clinical Chemistry Amsterdam Gastroenterology & Metabolism, Amsterdam UMC, University of Amsterdam Amsterdam The Netherlands.
  • Bouva MJ; Reference Laboratory Neonatal Screening, Center for Health protection National Institute for Public Health and the Environment Bilthoven The Netherlands.
  • De Sain-van der Velden M; Section Metabolic Diagnostics, Department of Genetics University Medical Center Utrecht Utrecht The Netherlands.
  • Schielen PCJI; Reference Laboratory Neonatal Screening, Center for Health protection National Institute for Public Health and the Environment Bilthoven The Netherlands.
  • Maase R; Reference Laboratory Neonatal Screening, Center for Health protection National Institute for Public Health and the Environment Bilthoven The Netherlands.
  • Engel H; Department of Clinical Chemistry Isala Hospital Zwolle The Netherlands.
  • Jakobs B; Department of Clinical Chemistry Elisabeth-Tweesteden Hospital Tilburg The Netherlands.
  • Kluijtmans LAJ; Translational Metabolic Laboratory, Department of Laboratory Medicine Radboud University Medical Center Nijmegen The Netherlands.
  • Mulder MF; Department of Pediatrics, Division of Metabolic Disorders Amsterdam UMC, Vrije Universiteit Amsterdam Amsterdam The Netherlands.
  • Rubio-Gozalbo ME; Department of Pediatrics and Clinical Genetics Maastricht University Medical Center Maastricht The Netherlands.
  • van Spronsen FJ; Division of Metabolic Disorders, Beatrix Children's Hospital University Medical Center Groningen, University of Groningen Groningen The Netherlands.
  • Visser G; Wilhelmina Children's Hospital University Medical Center Utrecht Utrecht The Netherlands.
  • de Vries MC; Department of Pediatrics, Division of Metabolic Disorders Radboud University Medical Center Nijmegen The Netherlands.
  • Williams M; Center for Lysosomal and Metabolic diseases, Department of Pediatrics Erasmus Medical Center Rotterdam The Netherlands.
  • Heijboer AC; Endocrinology Laboratory, Department of Clinical Chemistry Amsterdam Gastroenterology & Metabolism, Amsterdam UMC, University of Amsterdam Amsterdam The Netherlands.
  • Kemper EA; Endocrinology Laboratory, Department of Clinical Chemistry Amsterdam Gastroenterology & Metabolism, Amsterdam UMC, Vrije Universiteit Amsterdam Amsterdam The Netherlands.
  • Bosch AM; Department of Clinical Chemistry IJsselland Hospital Capelle aan den IJssel The Netherlands.
JIMD Rep ; 54(1): 68-78, 2020 Jul.
Article en En | MEDLINE | ID: mdl-32685353
ABSTRACT
Maple syrup urine disease (MSUD) leads to severe neurological deterioration unless diagnosed early and treated immediately. We have evaluated the effectiveness of 11 years of MSUD newborn screening (NBS) in the Netherlands (screening >72 hours, referral if both total leucine (Xle) and valine ≥400 µmol/L blood) and have explored possibilities for improvement by combining our data with a systematic literature review and data from Collaborative Laboratory Integrated Reports (CLIR). Dutch MSUD NBS characteristics and accuracy were determined. The hypothetical referral numbers in the Dutch population of additional screening markers suggested by CLIR were calculated. In a systematic review, articles reporting NBS leucine concentrations of confirmed patients were included. Our data showed that NBS of 1 963 465 newborns identified 4 MSUD patients and led to 118 false-positive referrals (PPV 3.28%; incidence 1491 000 newborns). In literature, leucine is the preferred NBS parameter. Total leucine (Xle) concentrations (mass-spectrometry) of 53 detected and 8 false-negative patients (sampling age within 25 hours in 3 patients) reported in literature ranged from 288 to 3376 (median 900) and 42 to 325 (median 209) µmol/L blood respectively. CLIR showed increasing Xle concentrations with sampling age and early NBS sampling and milder variant MSUD phenotypes with (nearly) normal biochemical profiles are causes of false-negative NBS results. We evaluated the effect of additional screening markers and established the Xle/phenylalanine ratio as a promising additional marker ratio for increasing the PPV, while maintaining high sensitivity in the Dutch MSUD NBS.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Diagnostic_studies / Prognostic_studies / Screening_studies / Systematic_reviews Idioma: En Revista: JIMD Rep Año: 2020 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Diagnostic_studies / Prognostic_studies / Screening_studies / Systematic_reviews Idioma: En Revista: JIMD Rep Año: 2020 Tipo del documento: Article