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Measures of gluten-related reactivity in children with autism spectrum disorders in the absence of overt gastrointestinal symptoms: a pilot study from the United Arab Emirates

OBJECTIVES: The aetiology of autism spectrum disorder (ASD) is multifactorial, sometimes genetic, and may be associated with abnormal immunological responses to peptides from proteins such as gluten. These peptides may cross the blood-brain barrier and affect neurotransmission, resulting in behaviou...

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Detalles Bibliográficos
Autores principales: Abdel-Maksoud, Mohamed, Aly El-Gabry, Dina, Al Kayoumi, Tahani, Alketbi, Jamila, Mohamednour, Duaa, Elhassan Elamin, Mohamed, Subhash Reddy, Marri, Al Yafei, Zain Ali, Stip, Emmanuel, Abdel Aziz, Karim, Arnone, Danilo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7513412/
https://www.ncbi.nlm.nih.gov/pubmed/32959707
http://dx.doi.org/10.1177/0300060520952655
Descripción
Sumario:OBJECTIVES: The aetiology of autism spectrum disorder (ASD) is multifactorial, sometimes genetic, and may be associated with abnormal immunological responses to peptides from proteins such as gluten. These peptides may cross the blood-brain barrier and affect neurotransmission, resulting in behavioural symptoms consistent with ASD. The aim of this study was to screen for markers of gluten-related immune reactivity in the absence of overt gastrointestinal symptoms in patients with ASD in the United Arab Emirates, a country associated with a high prevalence of ASD but lacking this type of research. METHODS: Patients diagnosed with ASD (using Diagnostic and Statistical Manual of Mental Disorders-IV-based criteria and Autism Diagnostic Observational Schedules) were compared with controls, regarding anti-tissue transglutaminase (tTG) immunoglobulin (Ig) A and anti-deamidated gliadin peptide (DGP) IgA levels. RESULTS: Sixty-six patients with ASD and 101 controls were included. Patients with ASD showed statistically significant lower anti-DGP IgA levels, but no significant difference in anti-tTG IgA levels, versus healthy controls. Correlations between immunological data and clinical symptoms were synergistic, but not statistically significant. CONCLUSION: ASD may be associated with reduced levels of anti-DGP IgA.