Neuropediatrics 2015; 46(06): 410-415
DOI: 10.1055/s-0035-1565273
Original Article
Georg Thieme Verlag KG Stuttgart · New York

Low Serum Level α-Synuclein and Tau Protein in Autism Spectrum Disorder Compared to Controls

Muhammed Tayyib Kadak
1   Department of Child and Adolescent Psychiatry, Cerrahpaşa School of Medicine, Istanbul University, Istanbul, Turkey
,
Ihsan Cetin
2   Department of Nutrition and Dietetics, School of Health, Batman University, Batman, Turkey
,
Mahmut Cem Tarakçıoğlu
3   Clinics of Child and Adolescent Psychiatry, Bakırköy Dr Sadi Konuk Training and Education Hospital, Istanbul, Turkey
,
Ömer Faruk Özer
4   Department of Biochemistry, Bezmi Alem Vakıf University, Istanbul, Turkey
,
Selma Kaçar
5   Department of Psychiatry, Cerrahpaşa School of Medicine, Istanbul University, Istanbul, Turkey
,
Behzat Çimen
6   Department of Biochemistry, Faculty of Pharmacy, Erciyes University, Kayseri, Turkey
› Institutsangaben
Weitere Informationen

Publikationsverlauf

27. Mai 2015

23. August 2015

Publikationsdatum:
19. Oktober 2015 (online)

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Abstract

α-Synuclein (α-syn) and tau proteins are thought to be related with the synaptic loss and cell death underlying several important neurodegenerative diseases. The aim of our study was to investigate serum α-syn and tau levels in autism. Serum levels of α-syn and tau were measured, and autism spectrum disorder (ASD) severity was assessed at admission using the Childhood Autism Rating Scale (CARS) total score. The mean CARS score of the autism group on admission was 47.91 points (SD: 5.97). The results indicated that the mean serum α-syn and serum tau levels were significantly (p < 0.001) lower in children with ASD as compared with normal cases (33.01 ± 20.78 and 55.19 ± 15.34 ng/mL and 241.23 ± 290.5 and 509.78 ± 269.25 ng/mL, respectively). There was a significant positive correlation between serum α-syn levels and serum levels of tau identified by Pearson correlation analysis (r = 0.922, n = 28, p < 0.001). Synaptic abnormality in autism may result from microglial activity. Furthermore, α-syn and tau aggregation may lead to synaptic dysfunction, and this may contribute to either neuronal or synaptic dysfunction or neurodegeneration. Our preliminary study suggests that low levels of serum α-syn and tau may be implicated in the relationship between synaptic activity and autism.