Department of Psychology and Logopedics, Faculty of Medicine, University of Helsinki, Helsinki, Finland; Faculty of Social Sciences, Health Sciences, University of Tampere, Tampere, Finland.
Department of Psychology and Logopedics, Faculty of Medicine, University of Helsinki, Helsinki, Finland.
J Affect Disord. 2018 Aug 1;235:480-488. doi: 10.1016/j.jad.2018.04.008. Epub 2018 Apr 6.
Lack of social support is an established risk factor across health outcomes, making it important to examine its family environmental and genetic determinants.
In a 27-year follow-up of the Young Finns Study (N = 2341), we examined with a latent growth curve model whether genes involved in the oxytocin signaling pathway-namely, oxytocin receptor gene (OXTR) variants rs1042778, rs2254298, and rs53576-moderate the effect of early-life social experiences on perceived social support across the life span. Mothers reported the emotional warmth and acceptance towards their children at baseline when the participants were from 3 to 18 years old (1980). Perceived family support and support from friends and peripheral sources were assessed in five follow-ups 18 years apart (1989-2007).
Maternal emotional warmth and acceptance predicted the initial level of perceived social support across subscales, while the rate of change in family support was affected by the family environment only if participants carried the T-allele of OXTR rs1042778. This gene-environment interaction was not found for the rate of change in support from friends and peripheral sources and we also did not find associations between latent growth in perceived social support and OXTR variants rs53576 and rs2254298.
Selective attrition in perceived social support, maternal emotional warmth and acceptance, gender, and SES. Family environment was assessed by a non-standardized measure.
OXTR rs1042778 polymorphism seems to contribute to changes in perceived family support in that way that some individuals (T-allele carriers) 'recover', to some extent, from the effects of early-life social experiences, whereas others (G/G genotype carriers) do not.
缺乏社会支持是影响健康结果的既定风险因素,因此研究其家庭环境和遗传决定因素非常重要。
在对青年芬兰人研究(N=2341)进行的 27 年随访中,我们使用潜在增长曲线模型研究了参与催产素信号通路的基因(即催产素受体基因(OXTR)变体 rs1042778、rs2254298 和 rs53576)是否会调节早期社会经历对整个生命周期感知社会支持的影响。当参与者年龄在 3 至 18 岁(1980 年)时,母亲报告了他们对孩子的情感温暖和接受程度。在五次相隔 18 年的随访中(1989-2007 年)评估了感知家庭支持以及来自朋友和外围来源的支持。
母亲的情感温暖和接受程度预测了感知社会支持各子量表的初始水平,而家庭支持的变化率仅在参与者携带 OXTR rs1042778 的 T 等位基因时才受到家庭环境的影响。这种基因-环境相互作用在来自朋友和外围来源的支持的变化率方面没有发现,我们也没有发现感知社会支持的潜在增长与 OXTR 变体 rs53576 和 rs2254298 之间的关联。
在感知社会支持、母亲情感温暖和接受程度、性别和 SES 方面存在选择性流失。家庭环境是通过非标准化测量来评估的。
OXTR rs1042778 多态性似乎对感知家庭支持的变化有一定的贡献,即某些个体(T 等位基因携带者)在某种程度上“从”早期社会经历的影响中“恢复”,而其他个体(G/G 基因型携带者)则没有。