Center for Psychiatric Neuroscience, Department of Psychiatry, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.
Service of Child and Adolescent Psychiatry, Department of Psychiatry, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.
Transl Psychiatry. 2024 Jan 17;14(1):30. doi: 10.1038/s41398-023-02728-4.
Adolescence is marked by the maturation of systems involved in emotional regulation and by an increased risk for internalizing disorders (anxiety/depression), especially in females. Hypothalamic-pituitary-adrenal (HPA)-axis function and redox homeostasis (balance between reactive oxygen species and antioxidants) have both been associated with internalizing disorders and may represent critical factors for the development of brain networks of emotional regulation. However, sex-specific interactions between these factors and internalizing symptoms and their link with brain maturation remain unexplored. We investigated in a cohort of adolescents aged 13-15 from the general population (n = 69) whether sex-differences in internalizing symptoms were associated with the glutathione (GSH)-redox cycle homeostasis and HPA-axis function and if these parameters were associated with brain white matter microstructure development. Female adolescents displayed higher levels of internalizing symptoms, GSH-peroxidase (GPx) activity and cortisol/11-deoxycortisol ratio than males. There was a strong correlation between GPx and GSH-reductase (Gred) activities in females only. The cortisol/11-deoxycortisol ratio, related to the HPA-axis activity, was associated with internalizing symptoms in both sexes, whereas GPx activity was associated with internalizing symptoms in females specifically. The cortisol/11-deoxycortisol ratio mediated sex-differences in internalizing symptoms and the association between anxiety and GPx activity in females specifically. In females, GPx activity was positively associated with generalized fractional anisotropy in widespread white matter brain regions. We found that higher levels of internalizing symptoms in female adolescents than in males relate to sex-differences in HPA-axis function. In females, our results suggest an important interplay between HPA-axis function and GSH-homeostasis, a parameter strongly associated with brain white matter microstructure.
青春期的特点是参与情绪调节的系统成熟,以及内化障碍(焦虑/抑郁)的风险增加,尤其是在女性中。下丘脑-垂体-肾上腺(HPA)轴功能和氧化还原稳态(活性氧和抗氧化剂之间的平衡)都与内化障碍有关,可能是情绪调节脑网络发展的关键因素。然而,这些因素与内化症状之间的性别特异性相互作用及其与大脑成熟的联系仍未得到探索。我们在一般人群中对 13-15 岁的青少年队列(n=69)进行了研究,即内化症状的性别差异是否与谷胱甘肽(GSH)-氧化还原循环稳态和 HPA 轴功能有关,以及这些参数是否与大脑白质微观结构的发育有关。女性青少年的内化症状、GSH-过氧化物酶(GPx)活性和皮质醇/11-脱氧皮质醇比值均高于男性。只有女性的 GPx 和 GSH 还原酶(Gred)活性之间存在很强的相关性。皮质醇/11-脱氧皮质醇比值与 HPA 轴活性相关,在两性中均与内化症状相关,而 GPx 活性仅与女性的内化症状相关。皮质醇/11-脱氧皮质醇比值介导了内化症状的性别差异,以及女性中焦虑与 GPx 活性之间的关联。在女性中,GPx 活性与广泛的白质脑区的全脑各向异性分数呈正相关。我们发现,女性青少年内化症状的水平高于男性,这与 HPA 轴功能的性别差异有关。在女性中,我们的结果表明 HPA 轴功能和 GSH 稳态之间存在重要的相互作用,GSH 稳态是与大脑白质微观结构密切相关的参数。