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Treatment Outcomes for Maple Syrup Urine Disease Detected by Newborn Screening.
Mengler, Katharina; Garbade, Sven F; Gleich, Florian; Thimm, Eva; May, Petra; Lindner, Martin; Lüsebrink, Natalia; Marquardt, Thorsten; Hübner, Vanessa; Krämer, Johannes; Neugebauer, Julia; Beblo, Skadi; Gillitzer, Claus; Grünert, Sarah C; Hennermann, Julia B; Kamrath, Clemens; Marquardt, Iris; Näke, Andrea; Murko, Simona; Schmidt, Sebastian; Schnabel, Elena; Lommer-Steinhoff, Svenja; Hoffmann, Georg F; Beime, Jan; Santer, René; Kölker, Stefan; Mütze, Ulrike.
Afiliação
  • Mengler K; Medical Faculty of Heidelberg, Center for Child and Adolescent Medicine, Division of Child Neurology and Metabolic Medicine, Heidelberg University, Heidelberg, Germany.
  • Garbade SF; Medical Faculty of Heidelberg, Center for Child and Adolescent Medicine, Division of Child Neurology and Metabolic Medicine, Heidelberg University, Heidelberg, Germany.
  • Gleich F; Medical Faculty of Heidelberg, Center for Child and Adolescent Medicine, Division of Child Neurology and Metabolic Medicine, Heidelberg University, Heidelberg, Germany.
  • Thimm E; Department of General Pediatrics, Neonatology, and Pediatric Cardiology, University Children's Hospital.
  • May P; Clinic for Gastroenterology, Hepatology and Infectious Diseases, University Hospital Düsseldorf, Medical Faculty of Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
  • Lindner M; Division of Pediatric Neurology, University Children's Hospital Frankfurt, Frankfurt, Germany.
  • Lüsebrink N; Division of Pediatric Neurology, University Children's Hospital Frankfurt, Frankfurt, Germany.
  • Marquardt T; Department of Pediatrics, University Hospital Muenster, Muenster, Germany.
  • Hübner V; Children's Hospital Reutlingen, Klinikum am Steinenberg, Reutlingen, Germany.
  • Krämer J; Department of Pediatric and Adolescent Medicine, University of Ulm, Ulm, Germany.
  • Neugebauer J; Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Department of Pediatric Gastroenterology, Nephrology and Metabolic Diseases, Center of Chronically Sick Children, Charité - Universitätsmedizin Berlin, Berlin, Germany.
  • Beblo S; Department of Women and Child Health, Hospital for Children and Adolescents, Center for Pediatric Research Leipzig (CPL), University Hospitals, University of Leipzig, Leipzig, Germany.
  • Gillitzer C; Children's Hospital Carl Gustav Carus, Technical University Dresden, Dresden, Germany.
  • Grünert SC; Department of General Pediatrics, Adolescent Medicine and Neonatology, Medical Center - University of Freiburg, Faculty of Medicine, Freiburg, Germany.
  • Hennermann JB; Villa Metabolica, Center for Pediatric and Adolescent Medicine, Mainz University Medical Center, Mainz, Germany.
  • Kamrath C; Center of Child and Adolescent Medicine, Justus Liebig University, Giessen, Germany.
  • Marquardt I; Department of Child Neurology, Children's Hospital Oldenburg, Oldenburg, Germany.
  • Näke A; Children's Hospital Carl Gustav Carus, Technical University Dresden, Dresden, Germany.
  • Murko S; Department of Pediatrics, University Medical Center Eppendorf, Hamburg, Germany.
  • Schmidt S; Clinic for Internal Medicine III, Endocrinology and Metabolic Diseases, University Hospital Jena.
  • Schnabel E; Medical Faculty of Heidelberg, Center for Child and Adolescent Medicine, Division of Child Neurology and Metabolic Medicine, Heidelberg University, Heidelberg, Germany.
  • Lommer-Steinhoff S; Medical Faculty of Heidelberg, Center for Child and Adolescent Medicine, Division of Child Neurology and Metabolic Medicine, Heidelberg University, Heidelberg, Germany.
  • Hoffmann GF; Medical Faculty of Heidelberg, Center for Child and Adolescent Medicine, Division of Child Neurology and Metabolic Medicine, Heidelberg University, Heidelberg, Germany.
  • Beime J; Department of Pediatrics, University Medical Center Eppendorf, Hamburg, Germany.
  • Santer R; Department of Pediatrics, University Medical Center Eppendorf, Hamburg, Germany.
  • Kölker S; Medical Faculty of Heidelberg, Center for Child and Adolescent Medicine, Division of Child Neurology and Metabolic Medicine, Heidelberg University, Heidelberg, Germany.
  • Mütze U; Medical Faculty of Heidelberg, Center for Child and Adolescent Medicine, Division of Child Neurology and Metabolic Medicine, Heidelberg University, Heidelberg, Germany.
Pediatrics ; 154(2)2024 Aug 01.
Article em En | MEDLINE | ID: mdl-38957900
ABSTRACT

OBJECTIVE:

Maple syrup urine disease (MSUD), a life-threatening metabolic disorder, is included in newborn screening (NBS) programs worldwide. The study aims to evaluate the impact of NBS on the long-term outcome of MSUD patients.

METHODS:

We performed a prospective, national, multicenter, observational study.

RESULTS:

In the studied NBS cohort (N = 33; 22 classic MSUD [cMSUD], 11 variant MSUD [vMSUD]; median age at last visit 10.4 years), 32 (97%) patients survived, 58% of them had normal cognitive functions (median IQ 87). Initial peak leucine increased linearly with age in cMSUD (median 1712 µmol/L), but not in vMSUD. Global IQ correlated inversely with the initial peak leucine concentration (P = .04; ß = -0.0081) and the frequency of decompensations (P = .02; ß = -9.133). A cluster analysis identified 2 subgroups differing in their long-term metabolic control (median leucine concentration 162 vs 278 µmol/L; P < .001). In cMSUD, lower leucine concentrations were associated with a higher IQ (95.5 vs 80; P = .008). Liver transplantation (median age 5.8 years) was not associated with better cognitive outcome. NBS is highly sensitive for cMSUD, but vMSUD might be missed (N = 2 missed by NBS).

CONCLUSIONS:

NBS and the early start of treatment improve survival and long-term outcome in individuals with cMSUD. Disease severity is an important modifier of outcome; however, the time to NBS report and the quality of long-term metabolic control had an independent impact on cognitive outcome, highlighting the importance of an early diagnosis and the quality of treatment.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Triagem Neonatal / Doença da Urina de Xarope de Bordo Limite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male / Newborn Idioma: En Revista: Pediatrics Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Alemanha

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Triagem Neonatal / Doença da Urina de Xarope de Bordo Limite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male / Newborn Idioma: En Revista: Pediatrics Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Alemanha