Evidence map›Paper›PMID 42583094›Full record

ArticleNoro psikiyatri arsivi2026

Investigating Serum miRNA Levels in Autistic Children with and without Bipolar Disorder: A Case-Control Study.

Hüsna Kaan, Ali Karayağmurlu, Canan Küçükgergin, İlknur Bingül, Nusret Soylu

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Article in Noro psikiyatri arsivi, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Hüsna KaanDepartment of Child and Adolescent Psychiatry, Basaksehir Cam and Sakura City Hospital, Istanbul, Turkiye.
Ali KarayağmurluDepartment of Child and Adolescent Psychiatry, Istanbul Medical Faculty, İstanbul University, Istanbul, Turkiye.
Canan KüçükgerginDepartment of Medical Biochemistry, Istanbul Medical Faculty, Istanbul University, Istanbul, Turkiye.
İlknur BingülDepartment of Medical Biochemistry, Istanbul Medical Faculty, Istanbul University, Istanbul, Turkiye.
Nusret SoyluDepartment of Child and Adolescent Psychiatry, Istanbul Medical Faculty, İstanbul University, Istanbul, Turkiye.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: The presence of bipolar disorder (BD) in individuals with ASD exacerbates social and cognitive impairments, complicates diagnosis and treatment. The aim of this study was to compare the serum levels of specific miRNAs between children with ASD with and without BD, and to explore their association with BD comorbidity in ASD. Method: A group of 41 pediatric patients with comorbid ASD + BD and a group of 47 pediatric patients with ASD without BD were included in the study. Serum miRNA levels were measured using quantitative real-time polymerase chain reactions, focusing specifically on miRNAs such as miR-132-5p, miR-134-5p, miR-206, and miR-126-5p. Results: The ASD + BD group exhibited significantly greater ASD severity than the ASD without BD group. Serum levels of miR-134-5p, miR-206, and miR-126-5p were all higher in the ASD + BD group than in the ASD without BD group (p=0.038, p=0.023, and p=0.026, respectively), while miR-132-5p levels were not significantly different (p=0.105). Furthermore, miR-134-5p levels were correlated with the frequency of manic episodes in the ASD + BD group (p=0.007). Conclusion: The study findings suggest that miRNAs may be involved in the pathophysiology of comorbid BD in children with ASD and may potentially represent candidate biomarkers for early diagnosis and intervention, thus contributing to improved clinical outcomes in this population. Further research is now needed to validate these findings and to understand the underlying mechanisms.

Indexed as

AutismBDNFbipolar disordersmiRNAVEGF

Identifiers

PMID42583094
PMCPMC13459178

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