Antineuronal antibodies and 8-OHdG an indicator of cerebellar dysfunction in autism spectrum disorder: a case?control study

dc.contributor.authorKilicaslan, Fethiye
dc.contributor.authorAyaydin, Hamza
dc.contributor.authorCelik, Hakim
dc.contributor.authorKutuk, Meryem Ozlem
dc.contributor.authorKandemir, Hasan
dc.contributor.authorKoyuncu, Ismail
dc.contributor.authorKirnit, Adnan
dc.date.accessioned2020-11-02T07:01:16Z
dc.date.available2020-11-02T07:01:16Z
dc.date.issued2019
dc.description.abstractObjectives: Autism spectrum disorder (ASD) is a neurodevelopmental disorder, that starts in early childhood and presents with deficiencies in social-communicational domains along with restricted and repetitive behaviours/interests. While genetic factors are dominant in its pathogenesis, many factors, including neurological, environmental and immunological have been identified. Furtheremore, although cerebellar dysfunction in the etiology of autism has been shown in different studies, the possible causes of the dysfunction and the role of neuroinflammation among these causes have not been clarified yet. Anti-Yo, anti-Hu, anti-Ri and anti-Amphiphysin antibodies have been found to be associated with cerebellar degeneration. The aim of the present study was to compare anti-Yo, anti-Hu, anti-Ri and anti- Amphiphysin antibodies and 8-OHdG values in blood using the ELISA method between ASD patients and healthy children to demonstrate the role of neuroinflammation as a potential cause of cerebellar dysfunction and DNA damage and evaluate the relationship between Childhood Autism Rating Scale (CARS) scores in children diagnosed with ASD and these parameters. Methods: Thirty-five consecutive children between the ages of 3 and 12 referred to the Child and Adolescent Psychiatry Outpatient Clinic of Harran University Hospital and diagnosed with ASD according to the DSM-5 diagnostic criteria were included in the study. The children did not have any chronic physical disorders and were treatment naive. Thirty-three healthy children between the ages of 3 and 12 without any physical or psychiatric disorders were included as the healthy control group. For psychiatric evaluation, a sociodemographic form and to measure the severity of autism, CARS was used. In the study, anti-Yo, anti-Hu, anti-Ri and anti-Amphiphysin antibodies and 8-OHdG values in blood were investigated using the ELISA method. Results: Thirty-five cases with autism (62.9% males) and thirty-three healthy controls (72.7% males) were included in the present study (p?=?0.385). The median age was 6.0 in the ASD group and 7.0 in the control group (p?=?0.146). Among ASD patients, anti-Ri antibody positivity was detected, while no anti-Ri antibody positivity was found in the control group (p?=?0.002). In the ASD group, the anti-Hu and 8-OHdG values were found to be significantly higher than those of the controls (p?<?0.001, p?=?0.001); no significant difference was found between the ASD and control groups with regard to the anti-Yo and anti-Amphiphysin values (p?=?0.113, p?=?0.275). Conclusions: The results of the present study suggest that antibodies against cerebellum may be present among children with ASD and DNA damage may occur due to oxidative stress.en_US
dc.identifier.endpage846en_US
dc.identifier.issn2475-0573en_US
dc.identifier.issue4en_US
dc.identifier.startpage840en_US
dc.identifier.urihttps://www.tandfonline.com/doi/pdf/10.1080/24750573.2019.1674241?needAccess=true&
dc.identifier.urihttp://hdl.handle.net/11727/4983
dc.identifier.volume29en_US
dc.identifier.wos000489516500001en_US
dc.language.isoengen_US
dc.relation.isversionof10.1080/24750573.2019.1674241en_US
dc.relation.journalPSYCHIATRY AND CLINICAL PSYCHOPHARMACOLOGYen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergien_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectAutismen_US
dc.subjectanti-Purkinje cell antibodiesen_US
dc.subject8-hydroxy-2-deoxyguanosineen_US
dc.subjectDNA damageen_US
dc.subjectcerebellumen_US
dc.subjectoxidative stressen_US
dc.titleAntineuronal antibodies and 8-OHdG an indicator of cerebellar dysfunction in autism spectrum disorder: a case?control studyen_US
dc.typearticleen_US

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