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
Kevin Stroek,
Anita Boelen,
Marelle J. Bouva,
Monique De Sain‐van der Velden,
Peter C. J. I. Schielen,
Rose Maase,
Henk Engel,
Bernadette Jakobs,
Leo A. J. Kluijtmans,
Margot F. Mulder,
M. E. Rubio‐Gozalbo,
Francjan J. vanSpronsen,
Gepke Visser,
Maaike C. deVries,
Monique Williams,
Annemieke C. Heijboer,
Evelien A. Kemper,
Annet M. Bosch
Affiliations
Kevin Stroek
Endocrinology Laboratory, Department of Clinical Chemistry Amsterdam Gastroenterology & Metabolism, Amsterdam UMC, University of Amsterdam Amsterdam The Netherlands
Anita Boelen
Endocrinology Laboratory, Department of Clinical Chemistry Amsterdam Gastroenterology & Metabolism, Amsterdam UMC, University of Amsterdam Amsterdam The Netherlands
Marelle J. Bouva
Reference Laboratory Neonatal Screening, Center for Health protection National Institute for Public Health and the Environment Bilthoven The Netherlands
Monique De Sain‐van der Velden
Section Metabolic Diagnostics, Department of Genetics University Medical Center Utrecht Utrecht The Netherlands
Peter C. J. I. Schielen
Reference Laboratory Neonatal Screening, Center for Health protection National Institute for Public Health and the Environment Bilthoven The Netherlands
Rose Maase
Reference Laboratory Neonatal Screening, Center for Health protection National Institute for Public Health and the Environment Bilthoven The Netherlands
Henk Engel
Department of Clinical Chemistry Isala Hospital Zwolle The Netherlands
Bernadette Jakobs
Department of Clinical Chemistry Elisabeth‐Tweesteden Hospital Tilburg The Netherlands
Leo A. J. Kluijtmans
Translational Metabolic Laboratory, Department of Laboratory Medicine Radboud University Medical Center Nijmegen The Netherlands
Margot F. Mulder
Department of Pediatrics, Division of Metabolic Disorders Amsterdam UMC, Vrije Universiteit Amsterdam Amsterdam The Netherlands
M. E. Rubio‐Gozalbo
Department of Pediatrics and Clinical Genetics Maastricht University Medical Center Maastricht The Netherlands
Francjan J. vanSpronsen
Division of Metabolic Disorders, Beatrix Children's Hospital University Medical Center Groningen, University of Groningen Groningen The Netherlands
Gepke Visser
Wilhelmina Children's Hospital University Medical Center Utrecht Utrecht The Netherlands
Maaike C. deVries
Department of Pediatrics, Division of Metabolic Disorders Radboud University Medical Center Nijmegen The Netherlands
Monique Williams
Center for Lysosomal and Metabolic diseases, Department of Pediatrics Erasmus Medical Center Rotterdam The Netherlands
Annemieke C. Heijboer
Endocrinology Laboratory, Department of Clinical Chemistry Amsterdam Gastroenterology & Metabolism, Amsterdam UMC, University of Amsterdam Amsterdam The Netherlands
Evelien A. Kemper
Department of Clinical Chemistry IJsselland Hospital Capelle aan den IJssel The Netherlands
Annet M. Bosch
Department of Pediatrics, Division of Metabolic Disorders Amsterdam UMC, University of Amsterdam Amsterdam The Netherlands
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 1:491 000 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.