童年虐待对抑郁和非抑郁老年人皮质醇水平和皮质醇觉醒反应的影响

I. Wielaard, R. Schaakxs, H. Comijs, M. Stek, D. Rhebergen
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引用次数: 21

摘要

摘要目的:童年虐待与以后生活中的抑郁有关。这可能与下丘脑-垂体-肾上腺(HPA)轴功能有关。因此,我们旨在研究童年虐待及其与抑郁症的相互作用对老年人皮质醇水平的影响。方法:采用荷兰老年人抑郁症研究(NESDO)中418名参与者(平均年龄70.8岁)的数据;187名参与者经历过童年虐待;309名参与者被诊断患有抑郁症。每天的皮质醇水平是用每个参与者的六份唾液样本来确定的。进行多元回归分析。结果:儿童虐待与早晨皮质醇水平之间存在显著的负相关。在非抑郁症患者中,心理虐待和性虐待都与HPA轴在觉醒时的更大动态有关。结论:儿童虐待与醒来时较低的基础皮质醇水平有关,与重度抑郁症(MDD)无关。在醒来后的一小时内,只有非抑郁参与者的下丘脑轴的反应性更高,这可能表明晚年抑郁改变了童年虐待对下丘脑轴的影响。有童年虐待史的老年人可能更容易受到压力或压力事件的负面影响,这反映在下丘脑轴的失调上。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The influence of childhood abuse on cortisol levels and the cortisol awakening response in depressed and nondepressed older adults
Abstract Objectives: Childhood abuse has been associated with depression in later life. This may be related to hypothalamic-pituitary-adrenal (HPA) axis functioning. Therefore we aimed to examine the impact of childhood abuse and its interaction with depression on cortisol levels in older adults. Methods: Data from 418 participants (mean age 70.8 years) in the Netherlands Study of Depression in Older Persons (NESDO) were used; 187 participants experienced childhood abuse; 309 participants had a diagnosis of depression. Diurnal cortisol levels were determined using six saliva samples from every participant. Multiple regression analyses were performed. Results: Significant negative associations between childhood abuse and morning cortisol levels were found. In nondepressed persons, both psychological and sexual abuse were associated with greater dynamics of the HPA axis in response to awakening. Conclusions: Childhood abuse is associated with lower basal cortisol levels at awakening irrespective of major depressive disorder (MDD). Higher reactivity of the HPA axis during the hour after awakening was found in nondepressed participants only, which might suggest that late-life depression modifies the effect of childhood abuse on the HPA axis. Older adults with a history of childhood abuse may be more negatively affected by stress or stressful events and this is reflected in dysregulation of the HPA axis.
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