Psychopathology · diagnosis
Post-traumatic stress disorder
A disorder in which, after a serious traumatic event, re-experiencing (memories, nightmares, repetition in play), avoidance, negative changes in thinking and mood, and hyperarousal last at least one month. The fear learning and extinction circuit stands out in the brain: the amygdala overreacts to threat, while the ventromedial PFC does not brake it enough and the hippocampus does not tell contexts apart well enough.
Clinical picture (children and adolescents)
- About 15.9% of trauma-exposed children and adolescents develop PTSD; the rate is higher after interpersonal trauma and in girls (32.9% in girls after interpersonal trauma, 8.4% in boys after non-interpersonal trauma) (Alisic et al., 2014; 43 samples, 3,563 people). A
- In young children, re-experiencing may appear as traumatic play, frightening dreams and behavioral regression; adolescents show a picture similar to adults, sometimes with self-harm and substance use. B
- Dissociative subtype: a sense of detachment from oneself or one's surroundings. B
- Common co-occurring conditions: depression, other anxiety disorders, ADHD-like attention problems, sleep disorders. A
Circuits and networks
- Amygdala: threat appraisal; in PTSD, an exaggerated response to threat cues. B
- Medial & Frontopolar Prefrontal Cortex (ventromedial PFC): recall of fear extinction and braking of the amygdala; its activity is reduced in PTSD. B
- Hippocampus: telling contexts apart ("this place is safe"); smaller in PTSD (Logue et al., 2018). A
- Anterior Cingulate Cortex and Insula: salience and bodily arousal. B
- Periaqueductal Gray, Hypothalamus & Pituitary, Locus Coeruleus: defense responses (flight, fight, freeze), the stress axis and noradrenergic arousal. B
- Networks: increased activity in the Salience network (salience) network and reduced connectivity within the Default mode network (DMN) have been reported. C
Neurotransmitter systems
- Noradrenaline (noradrenaline): hyperarousal and startle; the locus coeruleus. B
- Stress axis (CRF, cortisol): regulation of the HPA axis is altered. B
- Serotonin (serotonin): SSRIs are effective in adults; the evidence in children is weak. B
Imaging and neurobiological findings
- ENIGMA-PGC (1,868 people, 794 with PTSD, 16 cohorts): in current PTSD the hippocampus is smaller than in trauma-exposed controls (d = −0.17); the amygdala difference (d = −0.11) is not significant after correction for multiple comparisons (Logue et al., 2018). A
- These are group-level differences; imaging cannot diagnose an individual. A
Developmental course
- Trauma during development can affect the maturation of prefrontal regulatory pathways and the stress axis; early intervention matters. B
- Most trauma-exposed children do not develop PTSD; a supportive caregiver is protective. B
Treatment and the systems it targets
- Trauma-focused cognitive behavioral therapy (TF-CBT) is first line in children and adolescents; an individual participant data meta-analysis found it effective regardless of age, sex and trauma type (de Haan et al., 2024). A
- Medication: in 131 children and adolescents, 10 weeks of sertraline did not beat placebo (Robb et al., 2010); SSRIs are not first choice in children but can be used for co-occurring depression and anxiety. B
- Exposure aims to strengthen fear extinction learning (vmPFC → amygdala). B
Link to the book (The Green Walnut on the Couch)
- In the book (translated from the Turkish original):
- FEAR system, clinical: "phobias, generalized anxiety, PTSD, behavioral inhibition".
- PAG, clinical: "PTSD and dissociation, selective mutism, exhaustion in depression, the EMDR hypothesis".
- Hippocampus, where it appears in the book: "chronic stress leading to a loss of contextualization (the “everywhere is dangerous” feeling in PTSD; Chapters 10 and 18)".
- Amygdala, where it appears in the book: "post-traumatic hippocampus-amygdala imbalance (Chapter 18)".
- Amygdala-hippocampus pathway: "contextual generalization in PTSD (Chapter 18)".
- Polyvagal hierarchy: "post-traumatic dissociation and the window of tolerance (Chapter 18)".
In the atlas
Regions
Core structures in bold.
Networks
Neurotransmitter pathways
Panksepp systems
References
- Alisic E et al. (2014). Rates of post-traumatic stress disorder in trauma-exposed children and adolescents: meta-analysis. British Journal of Psychiatry, 204(5), 335–340. Search PubMed
- Logue MW et al. (2018). Smaller hippocampal volume in posttraumatic stress disorder: a multisite ENIGMA-PGC study. Biological Psychiatry, 83(3), 244–253. Search PubMed
- Robb AS et al. (2010). Sertraline treatment of children and adolescents with posttraumatic stress disorder: a double-blind, placebo-controlled trial. Journal of Child and Adolescent Psychopharmacology, 20(6), 463–471. Search PubMed
- de Haan A et al. (2024). Efficacy and moderators of efficacy of cognitive behavioural therapies with a trauma focus in children and adolescents: an individual participant data meta-analysis of randomised trials. The Lancet Child & Adolescent Health, 8(1), 28–39. DOI: 10.1016/S2352-4642(23)00253-5.
This page was prepared from a literature review; it is for education and must not be used on its own for diagnosis or treatment decisions. Evidence level: A large consortium, meta-analysis or regulatory decision; B replicated studies or classic case; C single or pioneering study. Region pages are in Turkish.
Last reviewed by the author: 12 October 2026