3.9 Article

Assessment of malondialdehyde levels, superoxide dismutase, and catalase activity in children with autism spectrum disorders

Journal

PSYCHIATRY AND CLINICAL PSYCHOPHARMACOLOGY
Volume 28, Issue 4, Pages 408-415

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1080/24750573.2018.1470360

Keywords

Autism spectrum disorder; biomarkers; malondialdehyde; oxidative stress; superoxide dismutase

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OBJECTIVE: Blood biomarkers for diseases have recently become a topic of great interest. Many studies of Autism Spectrum Disorder (ASD) have been made to date looking for biomarkers in peripheral tissues, but no specific biomarker has yet been found. The aim of this study was to examine oxidative stress parameters including malondialdehyde (MDA) levels, superoxide dismutase (SOD), and catalase (CAT) activity and to determine both their sensitivity and specificity as biomarkers associated with oxidative stress in ASD. METHODS: This study measured the plasma MDA levels, SOD, and CAT activities in erythrocyte in 52 patients with ASD (aged 3-6 years) and in 48 age- and gender-matched healthy controls. ASD severity was rated using the Childhood Autism Rating Scale (CARS). RESULTS: MDA levels, SOD, and CAT activity were significantly higher in patients with ASD in comparison to the controls (p < .001). The receiver operator characteristic curve analysis showed a high diagnostic value for MDA, SOD, and CAT. Their areas under curve (AUC) were 0.937, 1.0, and 1.0, respectively (p < .001). A positive statistically significant correlation was determined between the total CARS score and MDA levels in ASD patients (r = 0.368, p = 0.007). CONCLUSION: This study shows that oxidative stress is higher in children with ASD. Increased vulnerability to oxidative stress may contribute to the development of ASD. Given the high sensitivity and specificity results, it is thought that these selected oxidative stress parameters could be important as biomarkers for ASD. Future studies should focus on the sensitivity and specificity of oxidative stress biomarkers in larger ASD populations.

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