大样本中无精神病理学人群唾液淀粉酶昼夜节律的决定因素。
Determinants of salivary evening α-amylase in a large sample free of psychopathology.
机构信息
Department of Psychiatry, VU University Medical Center, Amsterdam, The Netherlands.
出版信息
Int J Psychophysiol. 2012 Apr;84(1):33-8. doi: 10.1016/j.ijpsycho.2012.01.005. Epub 2012 Jan 23.
OBJECTIVE
Recently, salivary alpha-amylase (sAA) has been proposed as a suitable index for sympathetic activity and dysregulation of the autonomic nervous system (ANS). Although determinants of sAA have been described, they have not been studied within the same study with a large sample size without potential disturbances of psychopathology. In this paper, we report about correlates of evening sAA in saliva.
METHODS
In 487 participants (mean age=42.9years, 59.8% female) without lifetime psychiatric disorders from the Netherlands Study of Depression and Anxiety (NESDA), sociodemographic, health and sampling determinants of sAA levels were examined using multivariable linear regression analysis. sAA was measured in two saliva samples that participants collected in the late evening, at 22:00h and 23:00h, after which these were averaged.
RESULTS
In multivariate analysis, age (β=0.20, p<0.001) and daily alcohol intake (β=-0.13, p=0.01) were independent determinants of evening sAA levels. Gender, allergy or lung disease, and the use of oral contraceptives were univariate correlates, but no longer associated with sAA in the multivariate model.
CONCLUSIONS
Age and alcohol use were identified as potential confounding factors that should be taken into account in epidemiologic studies that examine the ANS function using sAA.
目的
最近,唾液α-淀粉酶(sAA)被认为是交感神经活动和自主神经系统(ANS)失调的合适指标。尽管已经描述了 sAA 的决定因素,但它们尚未在没有潜在精神病理学干扰的同一研究中,在具有大样本量的情况下进行研究。在本文中,我们报告唾液中 sAA 的傍晚相关因素。
方法
在来自荷兰抑郁与焦虑研究(NESDA)的 487 名无终生精神障碍的参与者(平均年龄=42.9 岁,59.8%为女性)中,使用多变量线性回归分析检查了 sAA 水平的社会人口统计学、健康和采样决定因素。参与者在晚上 10 点和 11 点收集了两个唾液样本,之后将这些样本平均化,以测量 sAA。
结果
在多变量分析中,年龄(β=0.20,p<0.001)和每日饮酒量(β=-0.13,p=0.01)是傍晚 sAA 水平的独立决定因素。性别、过敏或肺部疾病以及口服避孕药的使用是单变量相关因素,但在多变量模型中不再与 sAA 相关。
结论
年龄和饮酒量被确定为使用 sAA 检查 ANS 功能的流行病学研究中应考虑的潜在混杂因素。