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

TL;DR
This study found that children with ADHD have higher levels of certain brain-related proteins and stress hormones compared to healthy children, suggesting altered brain development and stress responses in ADHD.
Contribution
The study identifies altered neurotrophic and HPA axis markers in drug-naive ADHD children, suggesting potential biological pathways in ADHD pathophysiology.
Findings
ADHD children had higher serum levels of BDNF, GDNF, VEGF, ACTH, and cortisol compared to healthy controls.
No significant correlation was found between neurotrophic factors, HPA axis hormones, and ADHD symptom severity scores.
The findings suggest parallel and partially independent mechanisms involving neurotrophic and HPA axis systems in ADHD.
Abstract
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. 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…
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Taxonomy
TopicsAttention Deficit Hyperactivity Disorder · Autism Spectrum Disorder Research · Stress Responses and Cortisol
