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Tryptophan status in autism spectrum disorder and the influence of supplementation on its level

Recent reports show that the worldwide incidence of autism spectrum disorder (ASD) is dramatically increasing, although ASD etiology and pathogenesis are still far to be fully elucidated. Some dietary-derived essential compounds, such as the amino acid tryptophan, appear to be impaired in patients w...

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Autores principales: Kałużna-Czaplińska, Joanna, Jóźwik-Pruska, Jagoda, Chirumbolo, Salvatore, Bjørklund, Geir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5596045/
https://www.ncbi.nlm.nih.gov/pubmed/28608247
http://dx.doi.org/10.1007/s11011-017-0045-x
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author Kałużna-Czaplińska, Joanna
Jóźwik-Pruska, Jagoda
Chirumbolo, Salvatore
Bjørklund, Geir
author_facet Kałużna-Czaplińska, Joanna
Jóźwik-Pruska, Jagoda
Chirumbolo, Salvatore
Bjørklund, Geir
author_sort Kałużna-Czaplińska, Joanna
collection PubMed
description Recent reports show that the worldwide incidence of autism spectrum disorder (ASD) is dramatically increasing, although ASD etiology and pathogenesis are still far to be fully elucidated. Some dietary-derived essential compounds, such as the amino acid tryptophan, appear to be impaired in patients with ASD. Tryptophan (Trp) plays a significant role in the human organism and serves as a precursor for a wide range of bioactive compounds, including major neurotransmitters. Research indicates that tryptophan might be deficient in subjects with ASD. Deficiency in the tryptophan level can be retrieved by investigating Trp levels or its major metabolite kynurenine in urines. The purpose of the present study is to quantify tryptophan content in urine samples (n = 236) of ASD patients, who underwent a supplemented dietary panel with B vitamins and magnesium, compared to controls (without this diet regimen). The samples were analyzed with gas chromatography-mass spectrometry. Additionally, the correlation between body mass index (BMI) and the level of this amino acid in urine was accomplished. Basic parameters of urine samples were also evaluated. Statistical evaluations in the concentration of tryptophan in ASD patients with different severity of symptoms were reported. A significant difference in tryptophan levels in all groups was observed. Supplementation with B vitamins and magnesium has an influence on the Trp concentration. Furthermore, no correlation between BMI and tryptophan levels was found. These results assess that the Trp level in ASD subjects is critical and that intake of B vitamins and magnesium with diet might influence its metabolic homeostasis.
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spelling pubmed-55960452017-09-26 Tryptophan status in autism spectrum disorder and the influence of supplementation on its level Kałużna-Czaplińska, Joanna Jóźwik-Pruska, Jagoda Chirumbolo, Salvatore Bjørklund, Geir Metab Brain Dis Original Article Recent reports show that the worldwide incidence of autism spectrum disorder (ASD) is dramatically increasing, although ASD etiology and pathogenesis are still far to be fully elucidated. Some dietary-derived essential compounds, such as the amino acid tryptophan, appear to be impaired in patients with ASD. Tryptophan (Trp) plays a significant role in the human organism and serves as a precursor for a wide range of bioactive compounds, including major neurotransmitters. Research indicates that tryptophan might be deficient in subjects with ASD. Deficiency in the tryptophan level can be retrieved by investigating Trp levels or its major metabolite kynurenine in urines. The purpose of the present study is to quantify tryptophan content in urine samples (n = 236) of ASD patients, who underwent a supplemented dietary panel with B vitamins and magnesium, compared to controls (without this diet regimen). The samples were analyzed with gas chromatography-mass spectrometry. Additionally, the correlation between body mass index (BMI) and the level of this amino acid in urine was accomplished. Basic parameters of urine samples were also evaluated. Statistical evaluations in the concentration of tryptophan in ASD patients with different severity of symptoms were reported. A significant difference in tryptophan levels in all groups was observed. Supplementation with B vitamins and magnesium has an influence on the Trp concentration. Furthermore, no correlation between BMI and tryptophan levels was found. These results assess that the Trp level in ASD subjects is critical and that intake of B vitamins and magnesium with diet might influence its metabolic homeostasis. Springer US 2017-06-12 2017 /pmc/articles/PMC5596045/ /pubmed/28608247 http://dx.doi.org/10.1007/s11011-017-0045-x Text en © The Author(s) 2017 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Article
Kałużna-Czaplińska, Joanna
Jóźwik-Pruska, Jagoda
Chirumbolo, Salvatore
Bjørklund, Geir
Tryptophan status in autism spectrum disorder and the influence of supplementation on its level
title Tryptophan status in autism spectrum disorder and the influence of supplementation on its level
title_full Tryptophan status in autism spectrum disorder and the influence of supplementation on its level
title_fullStr Tryptophan status in autism spectrum disorder and the influence of supplementation on its level
title_full_unstemmed Tryptophan status in autism spectrum disorder and the influence of supplementation on its level
title_short Tryptophan status in autism spectrum disorder and the influence of supplementation on its level
title_sort tryptophan status in autism spectrum disorder and the influence of supplementation on its level
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5596045/
https://www.ncbi.nlm.nih.gov/pubmed/28608247
http://dx.doi.org/10.1007/s11011-017-0045-x
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