心理与行为研究 ›› 2026, Vol. 24 ›› Issue (1): 78-86.DOI: 10.12139/j.1672-0628.2026.01.009

• 发展与教育心理学 • 上一篇    下一篇

HPA轴系统多基因-亲子关系交互对青少年抑郁发展影响及性别差异

曾子豪1,2,3, 何震1, 袁言云1, 赵纤1, 印利红1, 谭嵘1, 常梦梦1, 胡义秋1,2,3,4   

  1. 1. 湖南师范大学教育科学学院,长沙 410081;
    2. 湖南省心理健康教育研究基地,长沙 410081;
    3. 认知与人类行为湖南省重点实验室,长沙 410081;
    4. 湖南师范大学心-脑交叉科学研究中心,长沙 410081
  • 收稿日期:2024-12-14 发布日期:2026-01-20
  • 通讯作者: 胡义秋
  • 基金资助:
    全国教育规划项目“健康中国背景下青少年抑郁的多模态体系研究”(BBA240039);湖南省教育厅项目优秀青年项目“多模态视角下基因-环境交互对青少年抑郁的综合影响研究”(24B0103)。

The Impact of HPA Axis System Polygenes and Parent-Child Interaction on Adolescent Depression Development and Gender Differences

ZENG Zihao1,2,3, HE Zhen1, YUAN Yanyun1, ZHAO Xian1, YIN Lihong1, TAN Rong1, CHANG Mengmeng1, HU Yiqiu1,2,3,4   

  1. 1. School of Educational Science, Hunan Normal University, Changsha 410081;
    2. China Research Center for Mental Health Education of Hunan Province, Changsha 410081;
    3. Cognition and Human Behavior Key Laboratory of Hunan Province, Changsha 410081;
    4. Center for Mind-Brain Science, Hunan Normal University, Changsha 410081
  • Received:2024-12-14 Published:2026-01-20

摘要: 抑郁是青少年常见的心理适应问题,其演变过程受到遗传易感性与家庭关系等因素的共同影响。本研究旨在考察HPA轴相关多基因与亲子互动之间的交互作用,如何影响青少年抑郁的发展路径。本研究采用纵向追踪设计,分三次时间节点收集594名初一年级学生的问卷数据与基因信息。通过潜变量增长模型,对青少年抑郁的起始状态及其变化速率进行分析,着重探讨基因与亲子关系的交互效应以及性别差异。结果表明,青少年抑郁呈现出逐渐上升的线性趋势,亲子关系预测青少年抑郁的初始水平。此外,HPA轴多基因评分与亲子关系之间的交互作用在预测青少年抑郁起始水平时呈现显著影响,但对随时间变化的增长速率不显著。性别差异分析显示,女生更易受到亲子关系和遗传因素的影响,这不仅体现在抑郁初始水平上,也影响其发展速度,结果提示干预措施应特别关注亲子关系和遗传风险的作用。

关键词: 青少年抑郁, HPA轴基因, 亲子关系, 发展轨迹

Abstract: The current study investigated the impact of the cumulative score of HPA-axis-related multilocus genetic profile scores (MGPS) and parent-child relationships on the developmental trajectory of adolescent depression. The sample consisted of 594 first-year students from a middle school in Hunan Province, China, collected through a longitudinal study design. Three waves of questionnaire data and genetic information were gathered. By using a latent growth curve model (LGCM), the initial levels and growth rates of adolescent depression were analyzed, with a particular focus on the interaction between genetic factors and parent-child relationships, as well as gender differences. Results indicated a linear increase in adolescent depression over time, and parent-child relationships significantly predicted the initial level of adolescent depression. Furthermore, the interaction between HPA-axis MGPS and parent-child relationships notably influenced the initial level of adolescent depression, but was not significantly associated with its growth rate over time. Gender analysis revealed that female adolescents were more susceptible to the combined influence of parent-child relationships and genetic factors, impacting both the initial levels and the developmental trajectory of adolescent depression. These findings suggest that intervention strategies should prioritize the roles of parent-child relationships and genetic vulnerability.

Key words: adolescent depression, HPA axis genes, parent-child relationships, developmental trajectory

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