Abnormal Prefrontal Development in Pediatric Posttraumatic Stress Disorder: A Longitudinal Structural and Functional Magnetic Resonance Imaging Study

被引:47
作者
Heyn, Sara A. [1 ,2 ]
Keding, Taylor J. [2 ]
Ross, Marisa C. [2 ]
Cisler, Josh M. [2 ,4 ]
Mumford, Jeanette A. [3 ]
Herringa, Ryan J. [2 ,4 ]
机构
[1] Univ Wisconsin, Neurosci & Publ Policy Program, Madison, WI 53719 USA
[2] Univ Wisconsin, Neurosci Training Program, Madison, WI 53719 USA
[3] Univ Wisconsin, Ctr Hlth Minds, Madison, WI 53719 USA
[4] Univ Wisconsin, Dept Psychiat, Sch Med & Publ Hlth, Madison, WI 53719 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
Childhood trauma; Functional magnetic resonance imaging; Neurodevelopment; Pediatric; Posttraumatic stress disorder; Structural magnetic resonance imaging; HIPPOCAMPAL VOLUME; HUMAN AMYGDALA; CHILDREN; EMOTION; PTSD; CORTEX; NEUROGENESIS; REAPPRAISAL; ADOLESCENTS; SCHEDULE;
D O I
10.1016/j.bpsc.2018.07.013
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
BACKGROUND: Prior studies of pediatric posttraumatic stress disorder (PTSD) have reported cross-sectional and age-related structural and functional brain abnormalities in networks associated with cognitive, affective, and self-referential processing. However, no reported studies have comprehensively examined longitudinal gray matter development and its intrinsic functional correlates in pediatric PTSD. METHODS: Twenty-seven youths with PTSD and 21 nontraumatized typically developing (TD) youths were assessed at baseline and 1-year follow-up. At each visit, youths underwent structural magnetic resonance imaging and resting-state functional magnetic resonance imaging. Regions with volumetric abnormalities in whole-brain structural analyses were identified and used as seeds in exploratory intrinsic connectivity analyses. RESULTS: Youths with PTSD exhibited sustained reductions in gray matter volume (GMV) in right ventromedial prefrontal cortex (PFC) and bilateral ventrolateral PFC. Group-by-time analyses revealed aberrant longitudinal development in dorsolateral PFC, where typically developing youths exhibited normative decreases in GMV between baseline and follow-up, and youths with PTSD showed increases in GMV. Using these regions as seeds, patients with PTSD exhibited atypical longitudinal decreases in intrinsic PFC-amygdala and PFC-hippocampus connectivity, in contrast to increases in typically developing youths. Specifically, youths with PTSD showed decreasing ventromedial PFC-amygdala connectivity as well as decreasing ventrolateral PFC-hippocampus connectivity over time. Notably, volumetric abnormalities in ventromedial PFC and ventrolateral PFC were predictive of symptom severity. CONCLUSIONS: These findings represent novel longitudinal volumetric and connectivity changes in pediatric PTSD. Atypical prefrontal GMV and prefrontal-amygdala/hippocampus development may underlie persistence of PTSD in youths and could serve as future therapeutic targets.
引用
收藏
页码:171 / 179
页数:9
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