Variability in medial prefrontal cortex responses to smiles in human infants is linked to genetic variation in the oxytocin system.

IF 2 4区 医学 Q4 NEUROSCIENCES
Social Neuroscience Pub Date : 2026-06-01 Epub Date: 2026-06-08 DOI:10.1080/17470919.2026.2686726
Tobias Grossmann
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引用次数: 0

Abstract

Smiling plays a critical role in guiding behavior during social interactions from early in human ontogeny. The current study examined whether genetic variation in the oxytocin system is linked to individual differences in medial prefrontal cortex (mPFC) responses to smiles in human infants. Results show that genetic variation in CD38 (rs3796863), linked in prior work to variation in oxytocin release, is associated with enhanced mPFC responses when 7-month-old infants were viewing smiles, but not when viewing angry or fearful faces. These findings provide novel evidence that oxytocin-related genetic variability contributes to early-emerging differences in social brain function and support the view that variability in processing of affiliative signals is influenced by neurogenetic mechanisms from early in human ontogeny.

婴儿内侧前额叶皮层对微笑的反应差异与催产素系统的遗传变异有关。
从人类个体发育的早期开始,微笑就在社会互动中起着指导行为的关键作用。目前的研究调查了催产素系统的遗传变异是否与婴儿内侧前额叶皮层(mPFC)对微笑反应的个体差异有关。结果表明,CD38 (rs3796863)的遗传变异与催产素释放的变异有关,当7个月大的婴儿看到微笑时,与mPFC反应增强有关,而在看到愤怒或恐惧的脸时则无关。这些发现提供了新的证据,证明催产素相关的遗传变异性有助于早期出现的社会脑功能差异,并支持了人类个体发育早期神经遗传机制影响亲和性信号处理变异性的观点。
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来源期刊
Social Neuroscience
Social Neuroscience 医学-神经科学
CiteScore
3.40
自引率
5.00%
发文量
36
审稿时长
6-12 weeks
期刊介绍: Social Neuroscience features original empirical Research Papers as well as targeted Reviews, Commentaries and Fast Track Brief Reports that examine how the brain mediates social behavior, social cognition, social interactions and relationships, group social dynamics, and related topics that deal with social/interpersonal psychology and neurobiology. Multi-paper symposia and special topic issues are organized and presented regularly as well. The goal of Social Neuroscience is to provide a place to publish empirical articles that intend to further our understanding of the neural mechanisms contributing to the development and maintenance of social behaviors, or to understanding how these mechanisms are disrupted in clinical disorders.
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