Relationship between Excreted Uremic Toxins and Degree of Disorder of Children with ASD

Author:

Osredkar Joško12ORCID,Baškovič Barbara Žvar1,Finderle Petra1ORCID,Bobrowska-Korczak Barbara3ORCID,Gątarek Paulina45,Rosiak Angelina45ORCID,Giebułtowicz Joanna6ORCID,Vrhovšek Maja Jekovec7,Kałużna-Czaplińska Joanna45ORCID

Affiliation:

1. Institute of Clinical Chemistry and Biochemistry, University Medical Center Ljubljana, Njegoseva 4, 1000 Ljubljana, Slovenia

2. Faculty of Pharmacy, University of Ljubljana, Aškerčeva Cesta 7, 1000 Ljubljana, Slovenia

3. Department of Toxicology and Food Science, Faculty of Pharmacy with the Laboratory Medicine Division, Medical University of Warsaw, Banacha 1, 02-097 Warsaw, Poland

4. Institute of General and Ecological Chemistry, Faculty of Chemistry, Lodz University of Technology, Zeromskiego 116, 90-924 Lodz, Poland

5. CONEM Poland Chemistry and Nutrition Research Group, Lodz University of Technology, Zeromskiego 116, 90-924 Lodz, Poland

6. Department of Bioanalysis and Drug Analysis, Faculty of Pharmacy with the Laboratory Medicine Division, Medical University of Warsaw, Banacha 1, 02-097 Warsaw, Poland

7. Center for Autism, Unit of Child Psychiatry, University Children’s Hospital, University Medical Centre Ljubljana, Zaloška c.002, 1000 Ljubljana, Slovenia

Abstract

Autism spectrum disorder (ASD) is a complex developmental disorder in which communication and behavior are affected. A number of studies have investigated potential biomarkers, including uremic toxins. The aim of our study was to determine uremic toxins in the urine of children with ASD (143) and compare the results with healthy children (48). Uremic toxins were determined with a validated high-performance liquid chromatography coupled to mass spectrometry (LC-MS/MS) method. We observed higher levels of p-cresyl sulphate (pCS) and indoxyl sulphate (IS) in the ASD group compared to the controls. Moreover, the toxin levels of trimethylamine N-oxide (TMAO), symmetric dimethylarginine (SDMA), and asymmetric dimethylarginine (ADMA) were lower in ASD patients. Similarly, for pCS and IS in children classified, according to the intensity of their symptoms, into mild, moderate, and severe, elevated levels of these compounds were observed. For mild severity of the disorder, elevated levels of TMAO and comparable levels of SDMA and ADMA for ASD children as compared to the controls were observed in the urine. For moderate severity of ASD, significantly elevated levels of TMAO but reduced levels of SDMA and ADMA were observed in the urine of ASD children as compared to the controls. When the results obtained for severe ASD severity were considered, reduced levels of TMAO and comparable levels of SDMA and ADMA were observed in ASD children.

Funder

Slovenian Research Agency

Publisher

MDPI AG

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis

Reference77 articles.

1. An Overview of Autism Spectrum Disorder, Heterogeneity and Treatment Options;Masi;Neurosci. Bull.,2017

2. Centers for Disease Control and Prevention (2023, January 08). Autism Spectrum Disorder (ASD). Data & Statistics on Autism Spectrum Disorder, Available online: https://www.cdc.gov/ncbddd/autism/data.html.

3. NIHM (2023, January 08). Mental Health Information. Autism Spectrum Disorder, Available online: https://www.nimh.nih.gov/health/topics/autism-spectrum-disorders-asd#part_145438.

4. Current Knowledge on the Genetics of Autism and Propositions for Future Research;Bourgeron;C. R. Biol.,2016

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