Literature DB >> 17216302

Pyridoxal 5'-phosphate may be curative in early-onset epileptic encephalopathy.

G F Hoffmann1, B Schmitt, M Windfuhr, N Wagner, H Strehl, S Bagci, A R Franz, P B Mills, P T Clayton, M R Baumgartner, B Steinmann, T Bast, N I Wolf, J Zschocke.   

Abstract

Neonatal epileptic encephalopathy can be caused by inborn errors of metabolism. These conditions are often unresponsive to treatment with conventional antiepileptic drugs. Six children with pyridox(am)ine-5'-phosphate oxidase (PNPO) deficiency presented with neonatal epileptic encephalopathy. Two were treated with pyridoxal 5'-phosphate (PLP) within the first month of life and showed normal development or moderate psychomotor retardation thereafter. Four children with late or no treatment died or showed severe mental handicap. All of the children showed atypical biochemical findings. Prompt treatment with PLP in all neonates and infants with epileptic encephalopathy should become mandatory, permitting normal development in at least some of those affected with PNPO deficiency.

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Year:  2006        PMID: 17216302     DOI: 10.1007/s10545-006-0508-4

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  9 in total

1.  Neonatal epileptic encephalopathy.

Authors:  P T Clayton; R A H Surtees; C DeVile; K Hyland; S J R Heales
Journal:  Lancet       Date:  2003-05-10       Impact factor: 79.321

2.  Mutations in antiquitin in individuals with pyridoxine-dependent seizures.

Authors:  Philippa B Mills; Eduard Struys; Cornelis Jakobs; Barbara Plecko; Peter Baxter; Matthias Baumgartner; Michèl A A P Willemsen; Heymut Omran; Uta Tacke; Birgit Uhlenberg; Bernhard Weschke; Peter T Clayton
Journal:  Nat Med       Date:  2006-02-19       Impact factor: 53.440

3.  Neonatal epileptic encephalopathy caused by mutations in the PNPO gene encoding pyridox(am)ine 5'-phosphate oxidase.

Authors:  Philippa B Mills; Robert A H Surtees; Michael P Champion; Clare E Beesley; Neil Dalton; Peter J Scambler; Simon J R Heales; Anthony Briddon; Irene Scheimberg; Georg F Hoffmann; Johannes Zschocke; Peter T Clayton
Journal:  Hum Mol Genet       Date:  2005-03-16       Impact factor: 6.150

4.  Pyridoxal phosphate de-activation by pyrroline-5-carboxylic acid. Increased risk of vitamin B6 deficiency and seizures in hyperprolinemia type II.

Authors:  R D Farrant; V Walker; G A Mills; J M Mellor; G J Langley
Journal:  J Biol Chem       Date:  2000-12-29       Impact factor: 5.157

5.  Pipecolic acid elevation in plasma and cerebrospinal fluid of two patients with pyridoxine-dependent epilepsy.

Authors:  B Plecko; S Stöckler-Ipsiroglu; E Paschke; W Erwa; E A Struys; C Jakobs
Journal:  Ann Neurol       Date:  2000-07       Impact factor: 10.422

6.  Pyridoxal phosphate is better than pyridoxine for controlling idiopathic intractable epilepsy.

Authors:  H-S Wang; M-F Kuo; M-L Chou; P-C Hung; K-L Lin; M-Y Hsieh; M-Y Chang
Journal:  Arch Dis Child       Date:  2005-05       Impact factor: 3.791

7.  Pyridoxal phosphate-responsive epilepsy with resistance to pyridoxine.

Authors:  Meng-Fai Kuo; Huei-Shyong Wang
Journal:  Pediatr Neurol       Date:  2002-02       Impact factor: 3.372

8.  Clinical and laboratory findings in twins with neonatal epileptic encephalopathy mimicking aromatic L-amino acid decarboxylase deficiency.

Authors:  C Bräutigam; K Hyland; R Wevers; R Sharma; L Wagner; G-J Stock; F Heitmann; G F Hoffmann
Journal:  Neuropediatrics       Date:  2002-06       Impact factor: 1.947

9.  Pyridoxine dependency: report of a case of intractable convulsions in an infant controlled by pyridoxine.

Authors:  A D HUNT; J STOKES; W W McCRORY; H H STROUD
Journal:  Pediatrics       Date:  1954-02       Impact factor: 7.124

  9 in total
  42 in total

Review 1.  Early-onset epileptic encephalopathies and the diagnostic approach to underlying causes.

Authors:  Su-Kyeong Hwang; Soonhak Kwon
Journal:  Korean J Pediatr       Date:  2015-11-22

2.  Treatable neonatal epilepsy.

Authors:  Robert Surtees; Nicole Wolf
Journal:  Arch Dis Child       Date:  2007-08       Impact factor: 3.791

3.  Pyridoxal phosphate dependency, a newly recognized treatable catastrophic epileptic encephalopathy.

Authors:  P L Pearl; S M Gospe
Journal:  J Inherit Metab Dis       Date:  2007-02       Impact factor: 4.982

Review 4.  The Impact of Next-Generation Sequencing on the Diagnosis and Treatment of Epilepsy in Paediatric Patients.

Authors:  Davide Mei; Elena Parrini; Carla Marini; Renzo Guerrini
Journal:  Mol Diagn Ther       Date:  2017-08       Impact factor: 4.074

5.  Molecular basis of reduced pyridoxine 5'-phosphate oxidase catalytic activity in neonatal epileptic encephalopathy disorder.

Authors:  Faik N Musayev; Martino L Di Salvo; Mario A Saavedra; Roberto Contestabile; Mohini S Ghatge; Alexina Haynes; Verne Schirch; Martin K Safo
Journal:  J Biol Chem       Date:  2009-09-15       Impact factor: 5.157

6.  Current treatment and management of pyridoxine-dependent epilepsy.

Authors:  Clara D M van Karnebeek; Sravan Jaggumantri
Journal:  Curr Treat Options Neurol       Date:  2015-02       Impact factor: 3.598

Review 7.  New treatment paradigms in neonatal metabolic epilepsies.

Authors:  P L Pearl
Journal:  J Inherit Metab Dis       Date:  2009-02-24       Impact factor: 4.982

8.  Normal Cerebrospinal Fluid Pyridoxal 5'-Phosphate Level in a PNPO-Deficient Patient with Neonatal-Onset Epileptic Encephalopathy.

Authors:  Alina Levtova; Stephane Camuzeaux; Anne-Marie Laberge; Pierre Allard; Catherine Brunel-Guitton; Paola Diadori; Elsa Rossignol; Keith Hyland; Peter T Clayton; Philippa B Mills; Grant A Mitchell
Journal:  JIMD Rep       Date:  2015-03-12

9.  Pyridoxine responsiveness in novel mutations of the PNPO gene.

Authors:  Barbara Plecko; Karl Paul; Philippa Mills; Peter Clayton; Eduard Paschke; Oliver Maier; Oswald Hasselmann; Gudrun Schmiedel; Simone Kanz; Mary Connolly; Nicole Wolf; Eduard Struys; Sylvia Stockler; Lucia Abela; Doris Hofer
Journal:  Neurology       Date:  2014-03-21       Impact factor: 9.910

10.  Genotypic and phenotypic spectrum of pyridoxine-dependent epilepsy (ALDH7A1 deficiency).

Authors:  Philippa B Mills; Emma J Footitt; Kevin A Mills; Karin Tuschl; Sarah Aylett; Sophia Varadkar; Cheryl Hemingway; Neil Marlow; Janet Rennie; Peter Baxter; Olivier Dulac; Rima Nabbout; William J Craigen; Bernhard Schmitt; François Feillet; Ernst Christensen; Pascale De Lonlay; Mike G Pike; M Imelda Hughes; Eduard A Struys; Cornelis Jakobs; Sameer M Zuberi; Peter T Clayton
Journal:  Brain       Date:  2010-06-16       Impact factor: 13.501

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