Could Fetuin-A Be a Biomarker for Autism Spectrum Disorder and Cognitive Developmental Delay?

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Özet

Abstract: Early detection of cognitive developmental delay (CDD) and autism spectrum disorder (ASD) is challenging, despite the numerous scientific studies conducted and different therapeutic strategies. Lack of a biomarker for autism is a limiting factor for early diagnosis, which could provide better outcome with early start of therapy. Because of the high serum fetuin-A concentration during intrauterine life, it has been suggested that fetuin-A may have a role in brain development. The current study sought to determine if fetuin-A, a multifunctional glycoprotein thought to have a role in brain development, may be used as a biomarker for the diagnosis of ASD and developmental delay. The study involved 55 children with cognitive developmental delays and 40 healthy children. Two categories of children with cognitive developmental delays were identified. The participants were subjected to a psychiatric assessment as well as developmental testing. Only 54.5% of the 55 individuals had CDD, whereas 45.5% had ASD. Using an ELISA kit, the levels of serum fetuin-A were determined spectrophotometrically. The serum fetuin-A levels in the patients from the test group were found to be significantly lower than in the healthy individuals (p < 0.001). The cutoff value for the serum fetuin-A levels for cognitive developmental delay and autism spectrum disorder was 518 µg/liter, according to the results of ROC analysis (84.6% sensitivity and 91.4% specificity, AUC: 0.95, p < 0.001). The findings suggest that the serum fetuin-A level may be used to diagnose autism spectrum disorder and cognitive developmental delays. © 2022, Pleiades Publishing, Ltd.

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RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/ebyu/12805Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.1134/s0006297922060074Yayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorKurt, Nezahat
dc.contributor.authorOzgeris, Fatma B.
dc.contributor.authorUcuz, Ilknur
dc.contributor.authorBayraktutan, Zafer
dc.contributor.authorKocak Yilmaz, Kubra
dc.contributor.authorDemirdogen, Esen Yildirim
dc.contributor.authorCayir, Atilla
dc.date.accessioned2026-10-18T20:27:40.461410246Z
dc.date.available2026-10-18T20:27:40.461410246Z
dc.date.issued2022
dc.description.abstractAbstract: Early detection of cognitive developmental delay (CDD) and autism spectrum disorder (ASD) is challenging, despite the numerous scientific studies conducted and different therapeutic strategies. Lack of a biomarker for autism is a limiting factor for early diagnosis, which could provide better outcome with early start of therapy. Because of the high serum fetuin-A concentration during intrauterine life, it has been suggested that fetuin-A may have a role in brain development. The current study sought to determine if fetuin-A, a multifunctional glycoprotein thought to have a role in brain development, may be used as a biomarker for the diagnosis of ASD and developmental delay. The study involved 55 children with cognitive developmental delays and 40 healthy children. Two categories of children with cognitive developmental delays were identified. The participants were subjected to a psychiatric assessment as well as developmental testing. Only 54.5% of the 55 individuals had CDD, whereas 45.5% had ASD. Using an ELISA kit, the levels of serum fetuin-A were determined spectrophotometrically. The serum fetuin-A levels in the patients from the test group were found to be significantly lower than in the healthy individuals (p < 0.001). The cutoff value for the serum fetuin-A levels for cognitive developmental delay and autism spectrum disorder was 518 µg/liter, according to the results of ROC analysis (84.6% sensitivity and 91.4% specificity, AUC: 0.95, p < 0.001). The findings suggest that the serum fetuin-A level may be used to diagnose autism spectrum disorder and cognitive developmental delays. © 2022, Pleiades Publishing, Ltd.
dc.identifier.doi10.1134/s0006297922060074
dc.identifier.eissn1608-3040
dc.identifier.endpage565
dc.identifier.issn0006-2979
dc.identifier.issue6
dc.identifier.pmid35790414
dc.identifier.scopus2-s2.0-85132272868
dc.identifier.startpage559
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/12805
dc.identifier.volume87
dc.identifier.wosWOS:000812254000007
dc.language.isoen
dc.publisherPleiades journals
dc.relation.ispartofBiochemistry (Moscow)
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectautistic spectrum disorder
dc.subjectbiomarker
dc.subjectcognitive developmental delay
dc.subjectfetuin-A
dc.subjectneurodevelopmental disorder
dc.subjectalpha-2-HS-Glycoprotein
dc.subjectAutism Spectrum Disorder
dc.subjectBiomarkers
dc.subjectChild
dc.subjectCognition
dc.subjectDevelopmental Disabilities
dc.subjectHumans
dc.subjectbiological marker
dc.subjectfetuin A
dc.subjectautism
dc.subjectdevelopmental disorder
dc.subjecthuman
dc.subjectpsychology
dc.titleCould Fetuin-A Be a Biomarker for Autism Spectrum Disorder and Cognitive Developmental Delay?
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus1
rdl.citation.wos2
rdl.departmentDepartment of Medical Biochemistry, Faculty of Medicine, Erzincan Binali Yildirim University, Erzincan, Turkey. nezahat.kurt@erzincan.edu.tr.
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)