Psychiatry and Clinical Psychopharmacology (Oct 2018)

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

  • Hatice Altun,
  • Nilfer Şahin,
  • Ergül Belge Kurutaş,
  • Umut Karaaslan,
  • Feyza Hatice Sevgen,
  • Ebru Fındıklı

DOI
https://doi.org/10.1080/24750573.2018.1470360
Journal volume & issue
Vol. 28, no. 4
pp. 408 – 415

Abstract

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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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