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Association Between Lysine Reduction Therapies and Cognitive Outcomes in Patients With Pyridoxine-Dependent Epilepsy.
Coughlin, Curtis R; Tseng, Laura A; Bok, Levinus A; Hartmann, Hans; Footitt, Emma; Striano, Pasquale; Tabarki, Brahim M; Lunsing, Roelineke J; Stockler-Ipsiroglu, Sylvia; Gordon, Shanlea; Van Hove, Johan L K; Abdenur, Jose E; Boyer, Monica; Longo, Nicola; Andrews, Ashley; Janssen, Mirian Ch; van Wegberg, Annemiek; Prasad, Chitra; Prasad, Asuri N; Lamb, Molly M; Wijburg, Frits A; Gospe, Sidney M; van Karnebeek, Clara.
Affiliation
  • Coughlin CR; Section of Clinical Genetics and Metabolism, Department of Pediatrics, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA curtis.coughlin@cuanschutz.edu.
  • Tseng LA; Department of Pediatrics, Emma Children's Hospital and Amsterdam Gastroenterology Endocrinology Metabolism, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, the Netherlands.
  • Bok LA; United for Metabolic Diseases, the Netherlands.
  • Hartmann H; Department of Pediatrics and Neonatology, Máxima Medical center, Veldhoven, the Netherlands.
  • Footitt E; Clinic for Pediatric Kidney, Liver, and Metabolic Diseases, Hannover Medical School, Hannover, Germany.
  • Striano P; Department of Metabolic Paediatrics, Great Ormond Street Hospital, London, UK.
  • Tabarki BM; Pediatric Neurology and Muscular Diseases Unit, IRCCS "G. Gaslini" Institute, Genova, Italy.
  • Lunsing RJ; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genova, Genova, Italy.
  • Stockler-Ipsiroglu S; Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
  • Gordon S; Department of Paediatric Neurology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
  • Van Hove JLK; Division of Biochemical Genetics, BC Children's Hospital, University of British Columbia, Vancouver, British Columbia, Canada.
  • Abdenur JE; BC Children's Hospital Research Institute, Vancouver, British Columbia, Canada.
  • Boyer M; Section of Clinical Genetics and Metabolism, Department of Pediatrics, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
  • Longo N; Division of Metabolic Disorders, CHOC Children's Hospital, Orange, California, USA.
  • Andrews A; Division of Metabolic Disorders, CHOC Children's Hospital, Orange, California, USA.
  • Janssen MC; Division of Medical Genetics, Department of Pediatrics, University of Utah, Salt Lake City, Utah, USA.
  • van Wegberg A; Division of Medical Genetics, Department of Pediatrics, University of Utah, Salt Lake City, Utah, USA.
  • Prasad C; Department of Internal Medicine, Radboud University Medical Center, Nijmegen, Gelderland, the Netherlands.
  • Prasad AN; Department of Gastroenterology and Hepatology, Dietetics and Intestinal Failure, Radboud University Medical Center, Nijmegen, Gelderland, the Netherlands.
  • Lamb MM; Department of Pediatrics, Western University, London, Ontario, Canada.
  • Wijburg FA; Department of Pediatrics, Western University, London, Ontario, Canada.
  • Gospe SM; Department of Epidemiology and Center for Global Health, Colorado School of Public Health, Aurora, Colorado, USA.
  • van Karnebeek C; Department of Pediatrics, Emma Children's Hospital and Amsterdam Gastroenterology Endocrinology Metabolism, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, the Netherlands.
Neurology ; 2022 Aug 25.
Article in En | MEDLINE | ID: mdl-36008148
ABSTRACT
BACKGROUND AND

OBJECTIVES:

Pyridoxine-dependent epilepsy (PDE-ALDH7A1) is a developmental epileptic encephalopathy characterized by seizure improvement after pyridoxine supplementation. Adjunct lysine reduction therapies reduce the accumulation of putative neurotoxic metabolites with the goal to improve developmental outcomes. Our objective was to examine the association between treatment with lysine reduction therapies and cognitive outcomes.

METHODS:

Participants were recruited from within the International Registry for Patients with Pyridoxine-Dependent Epilepsy from August 2014 through March 2021. The primary outcome was standardized developmental test scores associated with overall cognitive ability. The relationship between test scores and treatment was analyzed with multivariable linear regression using a mixed-effects model. A priori, we hypothesized that treatment in early infancy with pyridoxine and lysine reduction therapies would result in a normal developmental outcome. A sub-analysis was performed to evaluate the association between cognitive outcome and lysine reduction therapies initiated in the first six months of life.

RESULTS:

A total of 112 test scores from 60 participants were available. On average, treatment with pyridoxine and lysine reduction therapies was associated with a non-significant increase of 6.9 points (95% CI -2.7 to 16.5) on developmental testing compared to treatment with pyridoxine alone. For the sub-analysis, a total of 14 developmental testing scores were available from 8 participants. On average, treatment with pyridoxine and lysine reduction therapies in the first six months of life was associated with a significant increase of 21.9 points (95% CI 1.7 to 42.0) on developmental testing.

DISCUSSION:

Pyridoxine and lysine reduction therapies at any age was associated with mild improvement in developmental testing and treatment in early infancy was associated with a clinically significant increase in developmental test scores. These results provide insight into the mechanism of intellectual and developmental disability in PDE-ALDH7A1 and emphasize the importance of treatment in early infancy with both pyridoxine and lysine reduction therapies. CLASSIFICATION OF EVIDENCE This study provides Class IV evidence that in PDE-ALDH7A1, pyridoxine plus lysine reduction therapies compared to pyridoxine alone is not significantly associated with overall higher developmental testing scores, but treatment in the first six months of life is associated with significantly higher developmental testing scores.

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies / Risk_factors_studies Language: En Journal: Neurology Year: 2022 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies / Risk_factors_studies Language: En Journal: Neurology Year: 2022 Type: Article Affiliation country: United States