Cargando…

Mechanism of nitrogen metabolism-related parameters and enzyme activities in the pathophysiology of autism

BACKGROUND: There is evidence that impaired metabolism play an important role in the etiology of many neuropsychiatric disorders. Although this has not been investigated to date, several recent studies proposed that nitrogen metabolism-related parameters may have a pathophysiological role in autism....

Descripción completa

Detalles Bibliográficos
Autores principales: Abu Shmais, Ghada A, Al-Ayadhi, Laila Y, Al-Dbass, Abeer M, El-Ansary, Afaf K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3374296/
https://www.ncbi.nlm.nih.gov/pubmed/22958401
http://dx.doi.org/10.1186/1866-1955-4-4
_version_ 1782235631333670912
author Abu Shmais, Ghada A
Al-Ayadhi, Laila Y
Al-Dbass, Abeer M
El-Ansary, Afaf K
author_facet Abu Shmais, Ghada A
Al-Ayadhi, Laila Y
Al-Dbass, Abeer M
El-Ansary, Afaf K
author_sort Abu Shmais, Ghada A
collection PubMed
description BACKGROUND: There is evidence that impaired metabolism play an important role in the etiology of many neuropsychiatric disorders. Although this has not been investigated to date, several recent studies proposed that nitrogen metabolism-related parameters may have a pathophysiological role in autism. METHODS: The study enrolled 20 Saudi boys with autism aged 4 to 12 years and 20 healthy controls matched for age and gender. Levels of creatine, urea, ammonia, gamma-aminobutyric acid (GABA), glutamate:glutamine (Glu:Gln) ratio, and enzymatic activities of glutamate dehydrogenase, 5'-nucleotidase, and adenosine deaminase (ADA) were determined in plasma samples from both groups. RESULTS: We found a significant elevation of creatine, 5'-nucleotidase, GABA, and glutamic acid and a significant decrease in the enzymatic activity of ADA and glutamine level in patients with autism compared with healthy controls. The most significant variation between the two groups was found in the Glu:Gln ratio. CONCLUSION: A raised Glu:Gln ratio together with positive correlations in creatine, GABA, and 5'-nucleotidase levels could contribute to the pathophysiology of autism, and might be useful diagnostic markers. The mechanism through which these parameters might be related to autism is discussed in detail.
format Online
Article
Text
id pubmed-3374296
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher Springer
record_format MEDLINE/PubMed
spelling pubmed-33742962012-06-28 Mechanism of nitrogen metabolism-related parameters and enzyme activities in the pathophysiology of autism Abu Shmais, Ghada A Al-Ayadhi, Laila Y Al-Dbass, Abeer M El-Ansary, Afaf K J Neurodev Disord Research BACKGROUND: There is evidence that impaired metabolism play an important role in the etiology of many neuropsychiatric disorders. Although this has not been investigated to date, several recent studies proposed that nitrogen metabolism-related parameters may have a pathophysiological role in autism. METHODS: The study enrolled 20 Saudi boys with autism aged 4 to 12 years and 20 healthy controls matched for age and gender. Levels of creatine, urea, ammonia, gamma-aminobutyric acid (GABA), glutamate:glutamine (Glu:Gln) ratio, and enzymatic activities of glutamate dehydrogenase, 5'-nucleotidase, and adenosine deaminase (ADA) were determined in plasma samples from both groups. RESULTS: We found a significant elevation of creatine, 5'-nucleotidase, GABA, and glutamic acid and a significant decrease in the enzymatic activity of ADA and glutamine level in patients with autism compared with healthy controls. The most significant variation between the two groups was found in the Glu:Gln ratio. CONCLUSION: A raised Glu:Gln ratio together with positive correlations in creatine, GABA, and 5'-nucleotidase levels could contribute to the pathophysiology of autism, and might be useful diagnostic markers. The mechanism through which these parameters might be related to autism is discussed in detail. Springer 2012 2012-02-13 /pmc/articles/PMC3374296/ /pubmed/22958401 http://dx.doi.org/10.1186/1866-1955-4-4 Text en Copyright ©2012 Abu Shmais 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
Abu Shmais, Ghada A
Al-Ayadhi, Laila Y
Al-Dbass, Abeer M
El-Ansary, Afaf K
Mechanism of nitrogen metabolism-related parameters and enzyme activities in the pathophysiology of autism
title Mechanism of nitrogen metabolism-related parameters and enzyme activities in the pathophysiology of autism
title_full Mechanism of nitrogen metabolism-related parameters and enzyme activities in the pathophysiology of autism
title_fullStr Mechanism of nitrogen metabolism-related parameters and enzyme activities in the pathophysiology of autism
title_full_unstemmed Mechanism of nitrogen metabolism-related parameters and enzyme activities in the pathophysiology of autism
title_short Mechanism of nitrogen metabolism-related parameters and enzyme activities in the pathophysiology of autism
title_sort mechanism of nitrogen metabolism-related parameters and enzyme activities in the pathophysiology of autism
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3374296/
https://www.ncbi.nlm.nih.gov/pubmed/22958401
http://dx.doi.org/10.1186/1866-1955-4-4
work_keys_str_mv AT abushmaisghadaa mechanismofnitrogenmetabolismrelatedparametersandenzymeactivitiesinthepathophysiologyofautism
AT alayadhilailay mechanismofnitrogenmetabolismrelatedparametersandenzymeactivitiesinthepathophysiologyofautism
AT aldbassabeerm mechanismofnitrogenmetabolismrelatedparametersandenzymeactivitiesinthepathophysiologyofautism
AT elansaryafafk mechanismofnitrogenmetabolismrelatedparametersandenzymeactivitiesinthepathophysiologyofautism