Is Serum Progranulin Level a Biomarker in Autism and Cognitive Development Disorders?

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Objective: Cognitive developmental delay is a picture of the group of early-onset chronic diseases that affect 1.5-10% of children. Autism spectrum disorders are neurodevelopmental diseases with a genetic basis and abnormal brain development, characterized by disorders in areas that make up interpersonal relationships, such as communication, social cognition, and processing of emotional signals. Immune system dysfunction is thought to play a role in the pathogenesis of some neurological disorders, including autism. Progranulin is thought to be a regulator of the innate immune response. The purpose of this study was to look at plasma levels of progranulin, an anti-inflammatory neurotrophic factor, in children with autism spectrum disorder and cognitive developmental delay. Materials and Methods: The study was conducted on 52 children who were patients and 35 healthy children. Of the 52 children of the patient group, 32 were diagnosed with CDD and 20 were diagnosed with cognitive developmental delay–autism spectrum disorder. Serum progranulin concentrations were measured using a human-specific sandwich enzyme-linked immunosorbent assay. Results: Serum progranulin concentration was statistically lower in the patient group (110.746 ± 26.04) than in the healthy control group (137.346 ± 30.02). There was a statistically significant difference between the groups in levels of serum progranulin (P = .000). Receiver operating characteristic analysis was performed to evaluate the potential of progranulin as a biomarker to distinguish patients with cognitive developmental delay–autism spectrum disorder from healthy children. It detected a moderate area under the curve (0.743 ± 0.06) value and a more significant P value for progranulin (P = .000). Conclusion: Progranulin deficiency in patients with autism spectrum disorder–cognitive developmental delay may result in decreased neurotrophic support for many years, with cumulative damage associated with unregulated inflammation that may play a role in autism spectrum disorder–cognitive developmental delay. We believe that low progranulin levels could be a biomarker for autism spectrum disorder–cognitive developmental delay. © 2022, AVES. All rights reserved.

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AlanDeğerDil
dc.contributor.authorÖzgeriş, Fatma Betül
dc.contributor.authorKurt, Nezahat
dc.contributor.authorUcuz, Ilknur Ibili
dc.contributor.authorYilmaz, Kübra Koçak
dc.contributor.authorKeleş, Mevlüt Sait
dc.contributor.authorÇayir, Atilla
dc.contributor.authorDursun, Onur Burak
dc.date.accessioned2026-10-18T20:27:43.796143969Z
dc.date.available2026-10-18T20:27:43.796143969Z
dc.date.issued2022
dc.description.abstractObjective: Cognitive developmental delay is a picture of the group of early-onset chronic diseases that affect 1.5-10% of children. Autism spectrum disorders are neurodevelopmental diseases with a genetic basis and abnormal brain development, characterized by disorders in areas that make up interpersonal relationships, such as communication, social cognition, and processing of emotional signals. Immune system dysfunction is thought to play a role in the pathogenesis of some neurological disorders, including autism. Progranulin is thought to be a regulator of the innate immune response. The purpose of this study was to look at plasma levels of progranulin, an anti-inflammatory neurotrophic factor, in children with autism spectrum disorder and cognitive developmental delay. Materials and Methods: The study was conducted on 52 children who were patients and 35 healthy children. Of the 52 children of the patient group, 32 were diagnosed with CDD and 20 were diagnosed with cognitive developmental delay–autism spectrum disorder. Serum progranulin concentrations were measured using a human-specific sandwich enzyme-linked immunosorbent assay. Results: Serum progranulin concentration was statistically lower in the patient group (110.746 ± 26.04) than in the healthy control group (137.346 ± 30.02). There was a statistically significant difference between the groups in levels of serum progranulin (P = .000). Receiver operating characteristic analysis was performed to evaluate the potential of progranulin as a biomarker to distinguish patients with cognitive developmental delay–autism spectrum disorder from healthy children. It detected a moderate area under the curve (0.743 ± 0.06) value and a more significant P value for progranulin (P = .000). Conclusion: Progranulin deficiency in patients with autism spectrum disorder–cognitive developmental delay may result in decreased neurotrophic support for many years, with cumulative damage associated with unregulated inflammation that may play a role in autism spectrum disorder–cognitive developmental delay. We believe that low progranulin levels could be a biomarker for autism spectrum disorder–cognitive developmental delay. © 2022, AVES. All rights reserved.
dc.description.sponsorshipThis study was partially supported by Ataturk University (Scientific Research Project, 2013/7).
dc.identifier.doi10.5152/eurasianjmed.2022.21292
dc.identifier.eissn1308-8742
dc.identifier.endpage48
dc.identifier.issn1308-8734
dc.identifier.issue1
dc.identifier.pmcidPMC9634887
dc.identifier.pmid35307629
dc.identifier.scopus2-s2.0-85125835664
dc.identifier.startpage48
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/12870
dc.identifier.volume54
dc.identifier.wosWOS:000776956600010
dc.language.isoen
dc.publisherAVES
dc.relation.ispartofEurasian Journal of Medicine
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectAutism spectrum disorders
dc.subjectCognitive developmental delay
dc.subjectProgranulin
dc.titleIs Serum Progranulin Level a Biomarker in Autism and Cognitive Development Disorders?
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus4
rdl.citation.trdizin2
rdl.citation.wos3
rdl.departmentÜSKÜDAR ÜNİVERSİTESİ
rdl.departmentT.C. SAĞLIK BAKANLIĞI
rdl.departmentİNÖNÜ ÜNİVERSİTESİ
rdl.departmentERZİNCAN BİNALİ YILDIRIM ÜNİVERSİTESİ
rdl.departmentATATÜRK ÜNİVERSİTESİ
rdl.departmentTanımlanmamış Kurum
rdl.oa.statusgold
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexTRDIZIN
rdl.source.indexPUBMED
rdl.wos.indexEmerging Sources Citation Index (ESCI)