| Literature DB >> 24268530 |
Sylvia Stockler-Ipsiroglu1, Clara van Karnebeek2, Nicola Longo3, G Christoph Korenke4, Saadet Mercimek-Mahmutoglu5, Iris Marquart4, Bruce Barshop6, Christiane Grolik7, Andrea Schlune8, Brad Angle9, Helena Caldeira Araújo10, Turgay Coskun11, Luisa Diogo12, Michael Geraghty13, Goknur Haliloglu11, Vassiliki Konstantopoulou14, Vincenzo Leuzzi15, Alina Levtova16, Jennifer Mackenzie17, Bruno Maranda18, Aizeddin A Mhanni19, Grant Mitchell20, Andrew Morris21, Theresa Newlove22, Deborah Renaud23, Fernando Scaglia24, Vassili Valayannopoulos25, Francjan J van Spronsen26, Krijn T Verbruggen26, Nataliya Yuskiv22, William Nyhan6, Andreas Schulze27.
Abstract
We collected data on 48 patients from 38 families with guanidinoacetate methyltransferase (GAMT) deficiency. Global developmental delay/intellectual disability (DD/ID) with speech/language delay and behavioral problems as the most affected domains was present in 44 participants, with additional epilepsy present in 35 and movement disorder in 13. Treatment regimens included various combinations/dosages of creatine-monohydrate, l-ornithine, sodium benzoate and protein/arginine restricted diets. The median age at treatment initiation was 25.5 and 39 months in patients with mild and moderate DD/ID, respectively, and 11 years in patients with severe DD/ID. Increase of cerebral creatine and decrease of plasma/CSF guanidinoacetate levels were achieved by supplementation with creatine-monohydrate combined with high dosages of l-ornithine and/or an arginine-restricted diet (250 mg/kg/d l-arginine). Therapy was associated with improvement or stabilization of symptoms in all of the symptomatic cases. The 4 patients treated younger than 9 months had normal or almost normal developmental outcomes. One with inconsistent compliance had a borderline IQ at age 8.6 years. An observational GAMT database will be essential to identify the best treatment to reduce plasma guanidinoacetate levels and improve long-term outcomes.Entities:
Keywords: Autism; Creatine deficiency; Magnetic resonance spectroscopy; Neurodevelopmental outcome; Speech delay; Treatment evidence
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Year: 2013 PMID: 24268530 DOI: 10.1016/j.ymgme.2013.10.018
Source DB: PubMed Journal: Mol Genet Metab ISSN: 1096-7192 Impact factor: 4.797