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Neuropsychological profile and clinical effects of arginine treatment in children with creatine transport deficiency

BACKGROUND: SLC6A8, an X-linked gene, encodes the creatine transporter (CRTR) and its mutations lead to cerebral creatine (Cr) deficiency which results in mental retardation, speech and language delay, autistic-like behaviour and epilepsy (CRTR-D, OMIM 300352). CRTR-D represents the most frequent Cr...

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Autores principales: Chilosi, Annamaria, Casarano, Manuela, Comparini, Alessandro, Battaglia, Francesca Maria, Mancardi, Margherita Maria, Schiaffino, Cristina, Tosetti, Michela, Leuzzi, Vincenzo, Battini, Roberta, Cioni, Giovanni
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3526552/
https://www.ncbi.nlm.nih.gov/pubmed/22713831
http://dx.doi.org/10.1186/1750-1172-7-43
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author Chilosi, Annamaria
Casarano, Manuela
Comparini, Alessandro
Battaglia, Francesca Maria
Mancardi, Margherita Maria
Schiaffino, Cristina
Tosetti, Michela
Leuzzi, Vincenzo
Battini, Roberta
Cioni, Giovanni
author_facet Chilosi, Annamaria
Casarano, Manuela
Comparini, Alessandro
Battaglia, Francesca Maria
Mancardi, Margherita Maria
Schiaffino, Cristina
Tosetti, Michela
Leuzzi, Vincenzo
Battini, Roberta
Cioni, Giovanni
author_sort Chilosi, Annamaria
collection PubMed
description BACKGROUND: SLC6A8, an X-linked gene, encodes the creatine transporter (CRTR) and its mutations lead to cerebral creatine (Cr) deficiency which results in mental retardation, speech and language delay, autistic-like behaviour and epilepsy (CRTR-D, OMIM 300352). CRTR-D represents the most frequent Cr metabolism disorder but, differently from Cr synthesis defects, that are partially reversible by oral Cr supplementation, does not respond to Cr treatment even if precociously administrated. The precursors of Cr are the non-essential amino acids Glycine (Gly) and Arginine (Arg), which have their own transporters at the brain–blood barrier level and, therefore, their supplementation appears an attractive and feasible therapeutic option aimed at stimulating Cr endogenous synthesis and, in this way, at overcoming the block of Cr transport within the brain. However, until now the effects of Arg and/or Gly supplementation on Cr brain levels and behaviour have been controversial. METHODS: In this study five Italian male patients affected by CRTR-D were supplemented with oral L-Arg at a dosage of 300 mg/kg/day divided into 3 doses, for 24–36 months. Biochemical and plasmatic amino acids examinations and thyroid hormone dosages were periodically performed. Moreover, Proton and Phosphorus Magnetic Resonance Spectroscopy (MRS) was monitored during follow-up in concurrence with neuropsychological evaluations. RESULTS: During L-Arg treatment a clinical improvement in motor skills and to a lesser extent in communication and attention was observed. In addition, all patients had a reduction in the number and frequency of epileptic seizures. Daily living skills appeared also to be positively influenced by L-Arg treatment. Moreover, Total Cr and especially PhosphoCr, evaluated by proton and phosphorus spectroscopy, showed a mild increase, although well below the normal range. CONCLUSION: This study provides information to support the effectiveness of L-Arg supplement treatment in CTRT-D patients; in fact the syndromic pattern of cognitive and linguistic deficit presented by CRTR-D patients was partially altered by L-Arg supplementation especially at a qualitative clinical level. Oral L-Arg may represent not only a protective factor towards a further cognitive decline, but can lead to the acquisition of new skills.
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spelling pubmed-35265522012-12-20 Neuropsychological profile and clinical effects of arginine treatment in children with creatine transport deficiency Chilosi, Annamaria Casarano, Manuela Comparini, Alessandro Battaglia, Francesca Maria Mancardi, Margherita Maria Schiaffino, Cristina Tosetti, Michela Leuzzi, Vincenzo Battini, Roberta Cioni, Giovanni Orphanet J Rare Dis Research BACKGROUND: SLC6A8, an X-linked gene, encodes the creatine transporter (CRTR) and its mutations lead to cerebral creatine (Cr) deficiency which results in mental retardation, speech and language delay, autistic-like behaviour and epilepsy (CRTR-D, OMIM 300352). CRTR-D represents the most frequent Cr metabolism disorder but, differently from Cr synthesis defects, that are partially reversible by oral Cr supplementation, does not respond to Cr treatment even if precociously administrated. The precursors of Cr are the non-essential amino acids Glycine (Gly) and Arginine (Arg), which have their own transporters at the brain–blood barrier level and, therefore, their supplementation appears an attractive and feasible therapeutic option aimed at stimulating Cr endogenous synthesis and, in this way, at overcoming the block of Cr transport within the brain. However, until now the effects of Arg and/or Gly supplementation on Cr brain levels and behaviour have been controversial. METHODS: In this study five Italian male patients affected by CRTR-D were supplemented with oral L-Arg at a dosage of 300 mg/kg/day divided into 3 doses, for 24–36 months. Biochemical and plasmatic amino acids examinations and thyroid hormone dosages were periodically performed. Moreover, Proton and Phosphorus Magnetic Resonance Spectroscopy (MRS) was monitored during follow-up in concurrence with neuropsychological evaluations. RESULTS: During L-Arg treatment a clinical improvement in motor skills and to a lesser extent in communication and attention was observed. In addition, all patients had a reduction in the number and frequency of epileptic seizures. Daily living skills appeared also to be positively influenced by L-Arg treatment. Moreover, Total Cr and especially PhosphoCr, evaluated by proton and phosphorus spectroscopy, showed a mild increase, although well below the normal range. CONCLUSION: This study provides information to support the effectiveness of L-Arg supplement treatment in CTRT-D patients; in fact the syndromic pattern of cognitive and linguistic deficit presented by CRTR-D patients was partially altered by L-Arg supplementation especially at a qualitative clinical level. Oral L-Arg may represent not only a protective factor towards a further cognitive decline, but can lead to the acquisition of new skills. BioMed Central 2012-06-19 /pmc/articles/PMC3526552/ /pubmed/22713831 http://dx.doi.org/10.1186/1750-1172-7-43 Text en Copyright ©2012 Chilosi et al.;licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Chilosi, Annamaria
Casarano, Manuela
Comparini, Alessandro
Battaglia, Francesca Maria
Mancardi, Margherita Maria
Schiaffino, Cristina
Tosetti, Michela
Leuzzi, Vincenzo
Battini, Roberta
Cioni, Giovanni
Neuropsychological profile and clinical effects of arginine treatment in children with creatine transport deficiency
title Neuropsychological profile and clinical effects of arginine treatment in children with creatine transport deficiency
title_full Neuropsychological profile and clinical effects of arginine treatment in children with creatine transport deficiency
title_fullStr Neuropsychological profile and clinical effects of arginine treatment in children with creatine transport deficiency
title_full_unstemmed Neuropsychological profile and clinical effects of arginine treatment in children with creatine transport deficiency
title_short Neuropsychological profile and clinical effects of arginine treatment in children with creatine transport deficiency
title_sort neuropsychological profile and clinical effects of arginine treatment in children with creatine transport deficiency
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3526552/
https://www.ncbi.nlm.nih.gov/pubmed/22713831
http://dx.doi.org/10.1186/1750-1172-7-43
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