Bae Yoon Ju, Stadelmann Stephanie, Klein Annette Maria, Jaeger Sonia, Hiemisch Andreas, Kiess Wieland, Ceglarek Uta, Gaudl Alexander, Schaab Michael, von Klitzing Kai, Thiery Joachim, Kratzsch Juergen, Döhnert Mirko
Institute of Laboratory Medicine, Clinical Chemistry and Molecular Diagnostics, University of Leipzig, Leipzig, Germany.
Department of Child and Adolescent Psychiatry, Psychotherapy and Psychosomatics, University of Leipzig, Leipzig, Germany; LIFE - Leipzig Research Center for Civilization Diseases, University of Leipzig, Leipzig, Germany.
J Psychiatr Res. 2015 Dec;71:78-88. doi: 10.1016/j.jpsychires.2015.09.013. Epub 2015 Sep 30.
Stress biomarkers of the autonomic nervous system and hypothalamic-pituitary-adrenal axis (HPA-axis) can be measured via alpha-amylase (AA) and cortisol and cortisone in saliva. Objectives were to determine 1) the response patterns of cortisol, cortisone, and AA under both circadian conditions and the Trier Social Stress Test for Children (TSST-C), 2) which reactivity index is most suitable to differentiate internalizing or externalizing disorders from controls, and to explore 3) the interaction between AA and cortisol in the presence of internalizing or externalizing disorders.
Saliva samples (n = 2893) from children with internalizing (n = 55) or externalizing disorders (n = 33) and healthy children (n = 81) were analyzed for cortisol, cortisone, and AA under circadian conditions and TSST-C.
Circadian rhythm of three biomarkers did not differ between diagnostic groups. Age and gender were significant predictors for cortisol and awakening time influenced all three biomarkers significantly. TSST-C responses appeared sequentially in the order of AA, cortisol, and cortisone. Trajectories of cortisol and cortisone responses, not in AA, were significantly lower in children with internalizing or externalizing disorders than in healthy children. Cortisol percentage increase appeared to be the most suitable reactivity index to detect the difference between the diagnostic groups. Internalizing disorders had a negative association between AA decrease and cortisol increase (β = -.199, p < .05, R(2) = .304). Externalizing disorders had a positive association between AA baseline and cortisol increase (β = .229, p < .05, R(2) = .304).
An altered HPA-axis response during stress might result from chronic allostatic load in internalizing disorders and underaroused stress response system in externalizing disorders.
自主神经系统和下丘脑 - 垂体 - 肾上腺轴(HPA 轴)的应激生物标志物可通过唾液中的α - 淀粉酶(AA)、皮质醇和可的松来测量。目的是确定:1)在昼夜节律条件和儿童特里尔社会应激测试(TSST - C)下皮质醇、可的松和 AA 的反应模式;2)哪种反应性指标最适合区分内化或外化障碍与对照组;3)探讨内化或外化障碍存在时 AA 与皮质醇之间的相互作用。
分析了内化障碍儿童(n = 55)、外化障碍儿童(n = 33)和健康儿童(n = 81)的唾液样本(n = 2893),以检测昼夜节律条件和 TSST - C 下的皮质醇、可的松和 AA。
诊断组之间三种生物标志物的昼夜节律无差异。年龄和性别是皮质醇的显著预测因素,觉醒时间对所有三种生物标志物均有显著影响。TSST - C 的反应按 AA、皮质醇和可的松的顺序依次出现。内化或外化障碍儿童的皮质醇和可的松反应轨迹(而非 AA)显著低于健康儿童。皮质醇百分比增加似乎是检测诊断组之间差异的最合适反应性指标。内化障碍中 AA 的降低与皮质醇的增加呈负相关(β = -.199,p <.05,R² =.304)。外化障碍中 AA 基线与皮质醇增加呈正相关(β =.229,p <.05,R² =.304)。
应激期间 HPA 轴反应的改变可能是由于内化障碍中的慢性应激负荷和外化障碍中应激反应系统激活不足所致。