ISSN 0439-755X
CN 11-1911/B
主办:中国心理学会
   中国科学院心理研究所
出版:科学出版社

心理学报

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多巴胺系统基因调节青少年同伴拒绝与亲社会行为关系:平行潜增长模型(亲社会行为专刊投稿)

李曦, 纪林芹, 迟晓慧, 王舒冉, 张文新, 曹衍淼   

  1. 山东师范大学心理学院
  • 收稿日期:2023-10-01 修回日期:2024-07-15 接受日期:2024-07-28
  • 通讯作者: 张文新
  • 基金资助:
    国家自然科学基金(32071073); 国家自然科学基金(31971008)

Dopaminergic genes moderated the association between peer rejection and adolescents’ prosocial behavior: Parallel latent growth modeling analyses

LI Xi, JI Linqin, CHI Xiaohui, WANG Shuran, ZHANG Wenxin, CAO Yanmiao   

  • Received:2023-10-01 Revised:2024-07-15 Accepted:2024-07-28
  • Contact: Zhang, zhang Wen-Xin

摘要: 基于动态发展和多基因研究视角,对1044名青少年(初测年龄13.32 ± 0.48岁, 50.1%女生)进行为期三年的追踪研究,考察青少年早期同伴拒绝的发展变化与亲社会行为发展变化的关系以及多巴胺系统基因的调节作用。结果发现:(1)青少年早期亲社会行为和同伴拒绝均呈线性上升趋势;(2)同伴拒绝的初始水平与增长速度均能影响亲社会行为发展轨迹。较高的同伴拒绝初始水平与较低的亲社会行为初始水平有关,也与更快的亲社会行为上升趋势有关,但是较高的同伴拒绝增长速度降低了亲社会行为的增长速度;(3)多巴胺系统多基因累加分能够调节同伴拒绝初始水平与亲社会行为初始水平、增长速度间的关系。相比携带较多高多巴胺含量相关等位基因的青少年,携带较少高多巴胺含量相关等位基因的青少年同伴拒绝初始水平越高,其亲社会行为初始水平更低、增长速度更快。

关键词: 亲社会行为, 同伴拒绝, 多巴胺系统基因×环境, 发展轨迹, 平行潜增长模型

Abstract: Prosocial behavior—behaviors intended to benefit others—is of particular importance to the development of children’s psychosocial functioning and has been a popular topic of research recently. Adolescence is a critical period for facilitating prosocial behavior and internalizing prosocial values because the ecological and biological transitions during adolescence play an important role in the development of prosocial behavior. Particularly, peer group changes and the increasing importance of peer relationships during this period provide both risks and opportunities for the development of prosocial behaviors. Moreover, individuals vary widely in their sensitivity to peer context. Recent evidence indicated that the genes involved in dopamine neurotransmission and metabolism act in an additive manner to influence sensitivity to the environment. It would be expected that dynamic changes in prosocial behavior over time would be related to both changing levels of peer environment and the person’s genetic predisposition. However, to our knowledge, no studies have investigated how dopaminergic genes and peer relationships interact to predict changes in prosocial behavior over time among adolescents. Therefore, the present study aimed to explore the dynamic trajectory of the relationship between peer rejection and prosocial behavior, and whether the dynamic association was moderated by dopaminergic genes. Participants were 1044 adolescents who were followed from age 13 to 15 (mean age 13.32 ± 0.48 years old at Time 1, 50.1% females). Adolescents’ saliva samples were collected at age 13. Saliva samples, peer-rated prosocial behavior, and peer-nomination peer rejection were collected. All measures showed good reliability. Genotyping was performed for each participant in real-time with MassARRAY RT software version 3.0.0.4 and analyzed using the MassARRAY Typer software version 3.4 (Sequenom). The parallel latent growth model and multiple group comparison analyses were used to examine the relationship between the developmental trajectories of peer rejection and prosocial behavior and the moderating role of dopaminergic genes. The results showed that adolescents’ prosocial behavior and peer rejection increased linearly during the follow-up period. Higher initial levels of peer rejection were associated with lower initial levels and slower growth of prosocial behavior. The change rates of peer relationships were associated with the developmental change of prosocial behavior, that is, the slower increase in peer rejection was associated with a greater increase in prosocial behavior over time. In addition, the relationships between the initial level of peer rejection and the initial level and growth in prosocial behavior were moderated by MGPS, with lower MGPS being more sensitive to the initial level of peer rejection. These findings lend support to the dynamic relationship between peer relationships and prosocial behavior and shed light on the complex polygenic underpinnings of prosocial behavior.

Key words: prosocial behavior, peer rejection, dopaminergic genes × environment, developmental trajectories, parallel latent growth modeling