Evidence map›Paper›PMID 41890430›Full record

ArticleFrontiers in psychiatry2026

Hypothalamic-pituitary-adrenal axis activity and neurotrophic factors in drug-naive children and adolescents with attention-deficit/hyperactivity disorder.

Hurşit Ferahkaya, Necati Uzun, Hasibe Ağır, İbrahim Kılınç, Abdullah Akkuş, Fatma Coşkun, Ömer Faruk Akça, Ayhan Bilgiç

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Article in Frontiers in psychiatry, 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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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Hurşit FerahkayaDepartment of Child and Adolescent Psychiatry, School of Medicine, Necmettin Erbakan University, Konya, Türkiye.
Necati UzunDepartment of Child and Adolescent Psychiatry, School of Medicine, Necmettin Erbakan University, Konya, Türkiye.
Hasibe AğırDepartment of Child and Adolescent Psychiatry, School of Medicine, Necmettin Erbakan University, Konya, Türkiye.
İbrahim KılınçDepartment of Biochemistry, School of Medicine, Necmettin Erbakan University, Konya, Türkiye.
Abdullah AkkuşDepartment of Pediatrics, School of Medicine, Necmettin Erbakan University, Konya, Türkiye.
Fatma CoşkunDepartment of Child and Adolescent Psychiatry, School of Medicine, Necmettin Erbakan University, Konya, Türkiye.
Ömer Faruk AkçaDepartment of Child and Adolescent Psychiatry, School of Medicine, Necmettin Erbakan University, Konya, Türkiye.
Ayhan BilgiçDepartment of Child and Adolescent Psychiatry, Izmir University of Economics, İzmir, Türkiye.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Attention deficit/hyperactivity disorder (ADHD) is a neurodevelopmental disorder with a complex and not fully understood etiology. Increasing evidence suggests that neurotrophic factors involved in neurodevelopment and synaptic plasticity, as well as hormones of the hypothalamic-pituitary-adrenal (HPA) axis that regulate the stress response, may contribute to the pathophysiology of ADHD. Methods: This cross-sectional study aimed to compare children diagnosed with ADHD and healthy controls with respect to serum levels of brain-derived neurotrophic factor (BDNF), glial cell line-derived neurotrophic factor (GDNF), vascular endothelial growth factor (VEGF), neurotrophin-3 (NT-3), adrenocorticotropic hormone (ACTH), and cortisol. A total of 80 children aged 6-18 years with a diagnosis of ADHD and 81 healthy controls were included in the study. The severity of ADHD symptoms was assessed using the Conners' Parent Rating Scale-Short Version (CPRS-SV). Serum levels of biochemical parameters were measured using commercially available electrochemiluminescence immunoassay and enzyme-linked immunosorbent assay kits. Results: Compared with the healthy control group, the ADHD group exhibited significantly higher serum levels of BDNF, GDNF, VEGF, ACTH, and cortisol, whereas NT-3 levels did not differ between the groups. These group differences remained statistically significant after controlling for potential confounding variables. Correlation analyses revealed no significant associations between neurotrophic factors, hypothalamic-pituitary-adrenal (HPA) axis hormones, and CPRS-SV subscale scores. Conclusions: The present findings indicate that neurotrophic factors and hormones related to the hypothalamic-pituitary-adrenal (HPA) axis are altered in medication-naïve children and adolescents with ADHD. The absence of a direct correlation between neurotrophic factors and HPA axis hormones suggests that these systems may contribute to the pathophysiology of ADHD through parallel yet partially independent and complex mechanisms. Future longitudinal and multimodal studies are warranted to elucidate the dynamic interactions between stress-related neuroendocrine processes and neurodevelopmental pathways in ADHD.

Indexed as

adrenocorticotropic hormoneattention-deficit/hyperactivity disordercortisolHPA axisneurotrophins

Identifiers

PMID41890430
PMCPMC13014257

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