European journal of psychotraumatology · 2026
FKBP5 methylation, temperament, and chronotype in adolescent posttraumatic stress disorder: a preliminary case-control study.
СтатьяНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Özaydın Yiğit, Özgür Börte Gürbüz, Özaydın Buket Canlan, Bozdoğan Bülent, Aksu Hatice
Аннотация
Background: Adolescents with posttraumatic stress disorder (PTSD) may show stress-system, personality, and circadian vulnerabilities, but these domains have rarely been examined together.Methods: In this exploratory case-control study, 36 newly diagnosed adolescents with DSM-5 PTSD, unmedicated at enrolment, and 36 trauma-unexposed controls (12-18 years) were assessed; diagnoses were confirmed with the K-SADS-PL. Symptom severity, temperament and character, and chronotype were measured with the Child PTSD Symptom Scale, the Junior Temperament and Character Inventory-Revised, and the Children's Chronotype Questionnaire. FKBP5 intron 7 methylation was assessed qualitatively at seven CpG sites by Sanger sequencing of bisulfite-converted PCR products.Results: Methylation positivity was observed in 27.8% of adolescents with PTSD and in 8.3% of controls (RR = 3.33, 95% BCa CI [0.96, 12.40]), a difference not robust across analytic approaches and reported as an effect-size estimate. The PTSD group showed higher Harm Avoidance, lower Self-Directedness and Cooperativeness, and greater eveningness. In multivariable analyses, lower Self-Directedness was independently associated with greater symptom severity (β = -.44), whereas methylation positivity showed a smaller association (β = .35; R² = .470) that did not persist under penalised estimation in the logistic model of case status.Conclusions: Methylation positivity and reduced Self-Directedness co-occurred with higher symptom burden. Because the controls were trauma-unexposed rather than trauma-exposed without PTSD, these differences distinguish adolescents with PTSD from trauma-naïve peers rather than marking PTSD specifically, and the qualitative assay indexes detectable methylation rather than methylation level. Replication with quantitative methylation measures, FKBP5 rs1360780 genotyping, trauma-exposed controls, and HPA-axis biomarkers is needed.