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Autism in patients with propionic acidemia.
Witters, Peter; Debbold, Eric; Crivelly, Kea; Vande Kerckhove, Kristel; Corthouts, Karen; Debbold, Brett; Andersson, Hans; Vannieuwenborg, Lena; Geuens, Sam; Baumgartner, Matthias; Kozicz, Tamas; Settles, Lisa; Morava, Eva.
Afiliação
  • Witters P; Department of Pediatrics, Metabolic Center, University Hospitals Leuven, Leuven, Belgium.
  • Debbold E; Hayward Genetics Center, Tulane University School of Medicine, New Orleans, LA, USA.
  • Crivelly K; Hayward Genetics Center, Tulane University School of Medicine, New Orleans, LA, USA.
  • Vande Kerckhove K; Department of Pediatrics, Metabolic Center, University Hospitals Leuven, Leuven, Belgium.
  • Corthouts K; Department of Pediatrics, Metabolic Center, University Hospitals Leuven, Leuven, Belgium.
  • Debbold B; Hayward Genetics Center, Tulane University School of Medicine, New Orleans, LA, USA.
  • Andersson H; Hayward Genetics Center, Tulane University School of Medicine, New Orleans, LA, USA.
  • Vannieuwenborg L; Department of Psychology, Metabolic Center, University Hospitals Leuven, Leuven, Belgium.
  • Geuens S; Department of Psychology, Metabolic Center, University Hospitals Leuven, Leuven, Belgium.
  • Baumgartner M; Division of Metabolism, Children's Research Center, University Children's Hospital Zurich, Zurich, Switzerland.
  • Kozicz T; Hayward Genetics Center, Tulane University School of Medicine, New Orleans, LA, USA; Donders Institute for Brain, Neuroscience, Radboudumc, Nijmegen, The Netherlands.
  • Settles L; Department of Psychiatry, Tulane University School of Medicine, New Orleans, LA, USA.
  • Morava E; Department of Pediatrics, Metabolic Center, University Hospitals Leuven, Leuven, Belgium; Hayward Genetics Center, Tulane University School of Medicine, New Orleans, LA, USA. Electronic address: emoravakozicz@tulane.edu.
Mol Genet Metab ; 119(4): 317-321, 2016 12.
Article em En | MEDLINE | ID: mdl-27825584
ABSTRACT
Certain inborn errors of metabolism have been suggested to increase the risk of autistic behavior. In an animal model, propionic acid ingestion triggered abnormal behavior resembling autism. So far only a few cases were reported with propionic acidemia and autistic features. From a series of twelve consecutively diagnosed cases with propionic acidemia, we report on eight patients with autistic features. The patients were followed 2-4 times a year and underwent regular clinical, dietary and laboratory investigations. Psychological evaluation was performed every second to fourth year. All patients were compliant with the standard diet and carnitine supplementation. None of the patients had frequent metabolic decompensations. From the metabolic factors known to impact neuropsychological outcome we detected chronically decreased valine levels and altered valine to leucine ratios in five out of the eight patients. Recurrent lactic acid elevations were present in six out of the eight patients. Five of the eight patients were diagnosed with Autism Spectrum Disorder, four of them had pathogenic variants in PCCB. Disorder according to DSM-IV and/or DSM-5 criteria. One of the patients diagnosed with propionic acidemia by newborn screening had the most significant behavioral features and another was diagnosed with Autism Spectrum Disorder prior to propionic acidemia. We hypothesize that chronic suboptimal intracellular metabolic balance may be responsible for the increased risk for autistic features in propionic acidemia. We propose that patients diagnosed with propionic acidemia should be screened for Autism Spectrum Disorder.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Triagem Neonatal / Metilmalonil-CoA Descarboxilase / Acidemia Propiônica / Transtorno do Espectro Autista Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Triagem Neonatal / Metilmalonil-CoA Descarboxilase / Acidemia Propiônica / Transtorno do Espectro Autista Idioma: En Ano de publicação: 2016 Tipo de documento: Article