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Untargeted metabolomics and infrared ion spectroscopy identify biomarkers for pyridoxine-dependent epilepsy.
Engelke, Udo Fh; van Outersterp, Rianne E; Merx, Jona; van Geenen, Fred Amg; van Rooij, Arno; Berden, Giel; Huigen, Marleen Cdg; Kluijtmans, Leo Aj; Peters, Tessa Ma; Al-Shekaili, Hilal H; Leavitt, Blair R; de Vrieze, Erik; Broekman, Sanne; van Wijk, Erwin; Tseng, Laura A; Kulkarni, Purva; Rutjes, Floris Pjt; Mecinovic, Jasmin; Struys, Eduard A; Jansen, Laura A; Gospe, Sidney M; Mercimek-Andrews, Saadet; Hyland, Keith; Willemsen, Michèl Aap; Bok, Levinus A; van Karnebeek, Clara Dm; Wevers, Ron A; Boltje, Thomas J; Oomens, Jos; Martens, Jonathan; Coene, Karlien Lm.
Afiliação
  • Engelke UF; Translational Metabolic Laboratory, Department of Laboratory Medicine, Radboud University Medical Center, Nijmegen, Netherlands.
  • van Outersterp RE; Institute for Molecules and Materials, FELIX Laboratory and.
  • Merx J; Institute for Molecules and Materials, Synthetic Organic Chemistry, Radboud University, Nijmegen, Netherlands.
  • van Geenen FA; Institute for Molecules and Materials, FELIX Laboratory and.
  • van Rooij A; Translational Metabolic Laboratory, Department of Laboratory Medicine, Radboud University Medical Center, Nijmegen, Netherlands.
  • Berden G; Institute for Molecules and Materials, FELIX Laboratory and.
  • Huigen MC; Translational Metabolic Laboratory, Department of Laboratory Medicine, Radboud University Medical Center, Nijmegen, Netherlands.
  • Kluijtmans LA; Translational Metabolic Laboratory, Department of Laboratory Medicine, Radboud University Medical Center, Nijmegen, Netherlands.
  • Peters TM; Translational Metabolic Laboratory, Department of Laboratory Medicine, Radboud University Medical Center, Nijmegen, Netherlands.
  • Al-Shekaili HH; Department of Neurology, Donders Institute for Brain, Cognition and Behavior, Radboud University Medical Center, Nijmegen, Netherlands.
  • Leavitt BR; Centre for Molecular Medicine and Therapeutics, British Columbia Children's Hospital Research Institute, Department of Medical Genetics, University of British Columbia Vancouver, British Columbia, Canada.
  • de Vrieze E; Centre for Molecular Medicine and Therapeutics, British Columbia Children's Hospital Research Institute, Department of Medical Genetics, University of British Columbia Vancouver, British Columbia, Canada.
  • Broekman S; Department of Otorhinolaryngology, Donders Institute for Brain, Cognition and Behavior, Radboud University Medical Center, Nijmegen, Netherlands.
  • van Wijk E; Department of Otorhinolaryngology, Donders Institute for Brain, Cognition and Behavior, Radboud University Medical Center, Nijmegen, Netherlands.
  • Tseng LA; Department of Otorhinolaryngology, Donders Institute for Brain, Cognition and Behavior, Radboud University Medical Center, Nijmegen, Netherlands.
  • Kulkarni P; Department of Pediatrics, Emma Children's Hospital, Amsterdam University Medical Centers, Amsterdam, Netherlands.
  • Rutjes FP; Translational Metabolic Laboratory, Department of Laboratory Medicine, Radboud University Medical Center, Nijmegen, Netherlands.
  • Mecinovic J; Institute for Molecules and Materials, Synthetic Organic Chemistry, Radboud University, Nijmegen, Netherlands.
  • Struys EA; Institute for Molecules and Materials, Synthetic Organic Chemistry, Radboud University, Nijmegen, Netherlands.
  • Jansen LA; Department of Physics, Chemistry and Pharmacy, University of Southern Denmark, Odense, Denmark.
  • Gospe SM; Department of Clinical Chemistry, Amsterdam University Medical Centers, location VU Medical Centre, Amsterdam, Netherlands.
  • Mercimek-Andrews S; Division of Pediatric Neurology, Washington University School of Medicine, St. Louis, Missouri, USA.
  • Hyland K; Departments of Neurology and Pediatrics, University of Washington, Seattle, Washington, USA.
  • Willemsen MA; Department of Pediatrics, Duke University, Durham, North Carolina, USA.
  • Bok LA; Division of Clinical and Metabolic Genetics, Department of Pediatrics, University of Toronto, Toronto, Ontario, Canada.
  • van Karnebeek CD; Department of Medical Genetics, University of Alberta, Edmonton, Alberta, Canada.
  • Wevers RA; Medical Neurogenetics Laboratories, Atlanta, Georgia, USA.
  • Boltje TJ; Department of Pediatric Neurology, Radboud University Medical Centre, Nijmegen, Netherlands.
  • Oomens J; Department of Pediatrics, Máxima Medical Centre, Veldhoven, Netherlands.
  • Martens J; Department of Pediatrics, Emma Children's Hospital, Amsterdam University Medical Centers, Amsterdam, Netherlands.
  • Coene KL; Department of Pediatrics-Metabolic Diseases, Radboud Center for Mitochondrial Medicine, Radboud University Medical Center, Nijmegen, Netherlands.
J Clin Invest ; 131(15)2021 08 02.
Article em En | MEDLINE | ID: mdl-34138754
BackgroundPyridoxine-dependent epilepsy (PDE-ALDH7A1) is an inborn error of lysine catabolism that presents with refractory epilepsy in newborns. Biallelic ALDH7A1 variants lead to deficiency of α-aminoadipic semialdehyde dehydrogenase/antiquitin, resulting in accumulation of piperideine-6-carboxylate (P6C), and secondary deficiency of the important cofactor pyridoxal-5'-phosphate (PLP, active vitamin B6) through its complexation with P6C. Vitamin B6 supplementation resolves epilepsy in patients, but intellectual disability may still develop. Early diagnosis and treatment, preferably based on newborn screening, could optimize long-term clinical outcome. However, no suitable PDE-ALDH7A1 newborn screening biomarkers are currently available.MethodsWe combined the innovative analytical methods untargeted metabolomics and infrared ion spectroscopy to discover and identify biomarkers in plasma that would allow for PDE-ALDH7A1 diagnosis in newborn screening.ResultsWe identified 2S,6S-/2S,6R-oxopropylpiperidine-2-carboxylic acid (2-OPP) as a PDE-ALDH7A1 biomarker, and confirmed 6-oxopiperidine-2-carboxylic acid (6-oxoPIP) as a biomarker. The suitability of 2-OPP as a potential PDE-ALDH7A1 newborn screening biomarker in dried bloodspots was shown. Additionally, we found that 2-OPP accumulates in brain tissue of patients and Aldh7a1-knockout mice, and induced epilepsy-like behavior in a zebrafish model system.ConclusionThis study has opened the way to newborn screening for PDE-ALDH7A1. We speculate that 2-OPP may contribute to ongoing neurotoxicity, also in treated PDE-ALDH7A1 patients. As 2-OPP formation appears to increase upon ketosis, we emphasize the importance of avoiding catabolism in PDE-ALDH7A1 patients.FundingSociety for Inborn Errors of Metabolism for Netherlands and Belgium (ESN), United for Metabolic Diseases (UMD), Stofwisselkracht, Radboud University, Canadian Institutes of Health Research, Dutch Research Council (NWO), and the European Research Council (ERC).
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ácidos Pipecólicos / Epilepsia / Metabolômica Tipo de estudo: Screening_studies Limite: Animals / Child / Female / Humans Idioma: En Revista: J Clin Invest Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Holanda

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ácidos Pipecólicos / Epilepsia / Metabolômica Tipo de estudo: Screening_studies Limite: Animals / Child / Female / Humans Idioma: En Revista: J Clin Invest Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Holanda