The effects of the COVID-19 pandemic on neurobiological functioning in adolescents.

IF 6.2 1区 医学 Q1 PSYCHIATRY
Justin P Yuan, Lauren R Borchers, Yoonji Lee, Jessica L Buthmann, Saché M Coury, Julian Joachimsthaler, Emma L Jaeger, Tiffany C Ho, Ian H Gotlib
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引用次数: 0

Abstract

The COVID-19 pandemic and its associated lockdowns were an unprecedented source of stress, with striking adverse effects on adolescents' mental health but relatively unknown effects on important aspects of neurobiological functioning. Using data from 154 adolescents (age M ± SD = 16.2 ± 1.1 years; range = 13.9-19.4) drawn from an ongoing longitudinal study and assessed either before or after the pandemic, we compared the pre-pandemic and post-pandemic groups on three key stress-sensitive biological systems: the hypothalamic-pituitary-adrenal (HPA) axis, immune response, and neural responses to affective stimuli. We found that compared to those assessed before the pandemic, adolescents assessed post-lockdown had significantly lower total cortisol production, elevated levels of systemic inflammation, and reduced neural activation in the prefrontal cortex during affective processing (pseudo-F(1,3250) = 7.43, p = 0.006). These findings suggest that, for adolescents, the experience of the pandemic was associated with significant disruptions in multiple biological systems that are sensitive to stress that might have enduring adverse developmental effects.

COVID-19大流行对青少年神经生物学功能的影响
COVID-19大流行及其相关的封锁是前所未有的压力来源,对青少年的心理健康产生了显著的不利影响,但对神经生物学功能的重要方面的影响相对未知。数据来自154名青少年(年龄M±SD = 16.2±1.1岁;范围= 13.9-19.4)),从正在进行的纵向研究中得出,并在大流行之前或之后进行评估,我们比较了大流行前和大流行后的三个关键应激敏感生物系统:下丘脑-垂体-肾上腺(HPA)轴、免疫反应和对情感刺激的神经反应。我们发现,与大流行前评估的青少年相比,封锁后评估的青少年皮质醇总量显著降低,全系统炎症水平升高,情感处理过程中前额皮质的神经激活减少(伪f (1,3250) = 7.43, p = 0.006)。这些发现表明,对于青少年来说,大流行的经历与对压力敏感的多种生物系统的严重破坏有关,这些生物系统可能对发育产生持久的不利影响。
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来源期刊
CiteScore
11.50
自引率
2.90%
发文量
484
审稿时长
23 weeks
期刊介绍: Psychiatry has suffered tremendously by the limited translational pipeline. Nobel laureate Julius Axelrod''s discovery in 1961 of monoamine reuptake by pre-synaptic neurons still forms the basis of contemporary antidepressant treatment. There is a grievous gap between the explosion of knowledge in neuroscience and conceptually novel treatments for our patients. Translational Psychiatry bridges this gap by fostering and highlighting the pathway from discovery to clinical applications, healthcare and global health. We view translation broadly as the full spectrum of work that marks the pathway from discovery to global health, inclusive. The steps of translation that are within the scope of Translational Psychiatry include (i) fundamental discovery, (ii) bench to bedside, (iii) bedside to clinical applications (clinical trials), (iv) translation to policy and health care guidelines, (v) assessment of health policy and usage, and (vi) global health. All areas of medical research, including — but not restricted to — molecular biology, genetics, pharmacology, imaging and epidemiology are welcome as they contribute to enhance the field of translational psychiatry.
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