Department of Psychology and Speech-Language Pathology, University of Turku, Assistentinkatu 7, 20520 Turku, Finland; Department of Psychology, University of Jyväskylä, Mattilanniemi 6, 40100 Jyväskylä, Finland; Centre of Excellence in Learning Dynamics and Intervention Research (InterLearn), University of Jyväskylä and University of Turku, Mattilanniemi 6, 40100 Jyväskylä, Finland; The FinnBrain Birth Cohort Study, Turku Brain and Mind Center, Department of Clinical Medicine, University of Turku, Kiinamyllynkatu 4-8, 20520 Turku, Finland; Centre for Population Health Research, University of Turku and Turku University Hospital, Kiinamyllynkatu 4-8, 20520 Turku, Finland.
The FinnBrain Birth Cohort Study, Turku Brain and Mind Center, Department of Clinical Medicine, University of Turku, Kiinamyllynkatu 4-8, 20520 Turku, Finland; Centre for Population Health Research, University of Turku and Turku University Hospital, Kiinamyllynkatu 4-8, 20520 Turku, Finland.
Psychoneuroendocrinology. 2023 Oct;156:106345. doi: 10.1016/j.psyneuen.2023.106345. Epub 2023 Jul 29.
This study performed latent profile analysis from more than 4000 saliva cortisol samples collected from children at the ages of 2 (T1), 3.5 (T2), and 5 years (T3). Three clearly different cortisol profiles were identified. The largest group at every age point was the Low/Regular latent profile, in which the cortisol slopes followed typical diurnal variation. A smaller proportion of the children belonged to the latent profile with relatively Low/Flat slope, and a minority belonged to the High/Fluctuating latent group, where the overall cortisol values and variations between the slopes were clearly higher than in the other groups. Most of the children who belonged to the High/Fluctuating group were cared for at home, they had higher temperamental surgency and their mothers had more depressive symptoms than in the other latent profile groups. However, only moderate intraindividual stability in diurnal cortisol profiles was observed across the follow-up period. On average, half of the children moved between the groups from T1 to T3. Neither child temperament, social competence, nor sex explained the stability or movement between the groups across age. Variations in cortisol profiles may be caused by the child's age, and diurnal cortisol rhythm becomes more regular along with development. Methodological issues regarding saliva cortisol research in young children are discussed. Also, more longitudinal research is needed to clarify mechanisms between environmental as well as individual factors and possible dysregulation in a child's HPA axis functioning.
本研究对 4000 多个儿童在 2 岁(T1)、3.5 岁(T2)和 5 岁(T3)时采集的唾液皮质醇样本进行了潜在剖面分析。确定了三种明显不同的皮质醇分布类型。在每个年龄点,最大的组是低/常规潜在分布组,其皮质醇斜率遵循典型的昼夜变化。较小比例的儿童属于相对低/平坦斜率的潜在分布组,少数儿童属于高/波动潜在分布组,其中皮质醇的整体水平和斜率之间的变化明显高于其他组。属于高/波动组的大多数儿童由母亲在家照顾,他们的气质活跃度较高,且其母亲的抑郁症状比其他潜在分布组更为明显。然而,在整个随访期间,仅观察到日间皮质醇分布的中等个体内稳定性。平均而言,一半的儿童在 T1 到 T3 期间从一个组转移到另一个组。儿童气质、社交能力或性别均不能解释各年龄组之间的稳定性或分组变化。皮质醇分布的变化可能是由儿童的年龄引起的,并且随着发育,昼夜皮质醇节律变得更加规律。文中还讨论了有关幼儿唾液皮质醇研究的方法学问题。此外,还需要更多的纵向研究来阐明环境和个体因素与儿童 HPA 轴功能可能失调之间的机制。