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SAL_15755 details
Primary information
SALIDSAL_15755
Biomarker nameOxytocin-neurophysin 1
Biomarker TypeNA
Sampling MethodASD age group: 11,7. TD group: 9,5, Inclusion criteria - DSM-IV-TR
Collection MethodSallivatte (Sarstedt, Rommelsdorft, Germany).
Analysis MethodSamples were concentrated by four (lyophilised), Protein measurements (ELISA kit), Sample concentrations (MATLAB 7)
Collection SiteWhole Saliva
Disease CategoryDevelopmental Disorder
Disease/ConditionAutism Spectrum Disorder
Disease SubtypeNA
Fold Change/ ConcentrationNA
Up/DownregulatedDownregulated
ExosomalNA
OrganismHomo sapiens
PMID24855128
Year of Publication2014
Biomarker IDP01178
Biomarker CategoryProtein
SequenceMAGPSLACCLLGLLALTSACYIQNCPLGGKRAAPDLDVRKCLPCGPGGKGRCFGPNICCAEELGCFVGTAEALRCQEENYLPSPCQSGQKACGSGGRCAVLGLCCSPDGCHADPACDAEATFSQR
Title of studyParent-child interaction and oxytocin production in pre-schoolers with autism spectrum disorder
Abstract of studyBACKGROUND: Autism spectrum disorder (ASD) is associated with genetic risk on the oxytocin system, suggesting oxytocin involvement in ASD; yet oxytocin functioning in young children with ASD is unknown.AIMS: To assess baseline oxytocin in pre-schoolers with ASD and test whether oxytocin production may be enhanced by parent-child contact.METHOD: Forty pre-schoolers with high-functioning ASD were matched with 40 typically developing controls. Two home visits included an identical 45-minute social battery once with the mother and once with the father. Four saliva oxytocin samples were collected from each parent and the child during each visit.RESULTS: Children with ASD had lower baseline oxytocin. Following 20 min of parent-child interactions, oxytocin normalised and remained high during social contact. Fifteen minutes after contact, oxytocin fell to baseline. Oxytocin correlated with parent-child social synchrony in both groups.CONCLUSIONS: Oxytocin dysfunction in ASD is observed in early childhood. The quick improvement in oxytocin production following parent-child contact underscores the malleability of the system and charts future directions for attachment-based behavioural and pharmacological interventions.