Aberrant Neural Response During Face Processing in Girls With Fragile X Syndrome: Defining Potential Brain Biomarkers for Treatment Studies

习惯化 心理学 脆性X综合征 自闭症 前额叶皮质 自闭症谱系障碍 焦虑 听力学 人口 神经科学 认知 发展心理学 医学 精神科 环境卫生
作者
Rihui Li,Jennifer Bruno,Tracy L. Jordan,Jonas G. Miller,Cindy H. Lee,Kristi L. Bartholomay,Matthew Marzelli,Aaron Piccirilli,Amy A. Lightbody,Allan L. Reiss
出处
期刊:Biological Psychiatry: Cognitive Neuroscience and Neuroimaging [Elsevier]
卷期号:8 (3): 311-319 被引量:3
标识
DOI:10.1016/j.bpsc.2021.09.003
摘要

Children and adolescents with fragile X syndrome (FXS) manifest significant symptoms of anxiety, particularly in response to face-to-face social interaction. In this study, we used functional near-infrared spectroscopy to reveal a specific pattern of brain activation and habituation in response to face stimuli in young girls with FXS, an important but understudied clinical population.Participants were 32 girls with FXS (age: 11.8 ± 2.9 years) and a control group of 28 girls without FXS (age: 10.5 ± 2.3 years) matched for age, general cognitive function, and autism symptoms. Functional near-infrared spectroscopy was used to assess brain activation during a face habituation task including repeated upright/inverted faces and greeble (nonface) objects.Compared with the control group, girls with FXS showed significant hyperactivation in the frontopolar and dorsal lateral prefrontal cortices in response to all face stimuli (upright + inverted). Lack of neural habituation (and significant sensitization) was also observed in the FXS group in the frontopolar cortex in response to upright face stimuli. Finally, aberrant frontopolar sensitization in response to upright faces in girls with FXS was significantly correlated with notable cognitive-behavioral and social-emotional outcomes relevant to this condition, including executive function, autism symptoms, depression, and anxiety.These findings strongly support a hypothesis of neural hyperactivation and accentuated sensitization during face processing in FXS, a phenomenon that could be developed as a biomarker end point for improving treatment trial evaluation in girls with this condition.
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