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Acute pediatric traumatic brain injury severity predicts long-term verbal memory performance through suppression by white matter integrity on diffusion tensor imaging.急性儿科创伤性脑损伤严重程度通过弥散张量成像中的白质完整性抑制预测长期言语记忆表现。
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Social brain, social dysfunction and social withdrawal.社会脑,社会功能障碍和社会退缩。
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Longitudinal Developmental Outcomes after Traumatic Brain Injury in Young Children: Are Infants More Vulnerable Than Toddlers?婴幼儿创伤性脑损伤后的纵向发育结果:婴儿比幼儿更脆弱吗?
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Neuropsychology's social landscape: Common ground with social neuroscience.神经心理学的社会图景:与社会神经科学的共同基础。
Neuropsychology. 2017 Nov;31(8):981-1002. doi: 10.1037/neu0000395.
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How Cells Fold the Cerebral Cortex.细胞如何折叠大脑皮层。
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How Forces Fold the Cerebral Cortex.力如何折叠大脑皮层。
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The Multifaceted Role of the Ventromedial Prefrontal Cortex in Emotion, Decision Making, Social Cognition, and Psychopathology.腹内侧前额叶皮层在情绪、决策、社会认知和精神病理学中的多方面作用。
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Psychosocial and Executive Function Recovery Trajectories One Year after Pediatric Traumatic Brain Injury: The Influence of Age and Injury Severity.儿童创伤性脑损伤后一年的心理社会和执行功能恢复轨迹:年龄和损伤严重程度的影响。
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Ten-year outcome of early childhood traumatic brain injury: Diffusion tensor imaging of the ventral striatum in relation to executive functioning.儿童期早期创伤性脑损伤的十年预后:腹侧纹状体的弥散张量成像与执行功能的关系
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儿童早期创伤性脑损伤后青少年皮质组织发育改变与社会化

Developmental Alterations in Cortical Organization and Socialization in Adolescents Who Sustained a Traumatic Brain Injury in Early Childhood.

机构信息

Department of Neurology, University of Utah, Salt Lake City, Utah, USA.

H. Ben Taub Department of Physical Medicine and Rehabilitation, Baylor College of Medicine, Houston, Texas, USA.

出版信息

J Neurotrauma. 2021 Jan 1;38(1):133-143. doi: 10.1089/neu.2019.6698. Epub 2020 Oct 6.

DOI:10.1089/neu.2019.6698
PMID:32503385
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7757621/
Abstract

This study investigated patterns of cortical organization in adolescents who had sustained a traumatic brain injury (TBI) during early childhood to determine ways in which early head injury may alter typical brain development. Increased gyrification in other patient populations is associated with polymicrogyria and aberrant development, but this has not been investigated in TBI. Seventeen adolescents (mean age = 14.1 ± 2.4) who sustained a TBI between 1-8 years of age, and 17 demographically-matched typically developing children (TDC) underwent a high-resolution, T1-weighted 3-Tesla magnetic resonance imaging (MRI) at 6-15 years post-injury. Cortical white matter volume and organization was measured using FreeSurfer's Local Gyrification Index (LGI). Despite a lack of significant difference in white matter volume, participants with TBI demonstrated significantly increased LGI in several cortical regions that are among those latest to mature in normal development, including left parietal association areas, bilateral dorsolateral and medial frontal areas, and the right posterior temporal gyrus, relative to the TDC group. Additionally, there was no evidence of increased surface area in the regions that demonstrated increased LGI. Higher Vineland-II Socialization scores were associated with decreased LGI in right frontal and temporal regions. The present results suggest an altered pattern of expected development in cortical gyrification in the TBI group, with changes in late-developing frontal and parietal association areas. Such changes in brain structure may underlie cognitive and behavioral deficits associated with pediatric TBI. Alternatively, increased gyrification following TBI may represent a compensatory mechanism that allows for typical development of cortical surface area, despite reduced brain volume.

摘要

本研究旨在调查儿童早期遭受创伤性脑损伤(TBI)的青少年的皮质组织模式,以确定早期头部损伤可能改变典型大脑发育的方式。在其他患者群体中,脑回增多与多微小脑回和发育异常有关,但尚未在 TBI 中进行研究。本研究共纳入 17 名青少年(平均年龄 14.1 ± 2.4 岁),这些患者在 1-8 岁时发生 TBI,以及 17 名年龄匹配的正常发育儿童(TDC)。所有参与者在伤后 6-15 年均接受了高分辨率 3T 磁共振成像(MRI)检查。使用 FreeSurfer 的局部脑回指数(LGI)来测量皮质白质体积和组织。尽管 TBI 组的白质体积无显著差异,但与 TDC 组相比,TBI 组在几个皮质区域的 LGI 显著增加,这些区域是正常发育中最晚成熟的区域之一,包括左侧顶叶联合区、双侧背外侧和内侧额区以及右侧颞后回。此外,在 LGI 增加的区域没有证据表明表面积增加。较高的 Vineland-II 社会适应评分与右额和颞区 LGI 降低有关。本研究结果表明,TBI 组的皮质脑回模式发生了改变,额叶和顶叶联合区的发育迟缓。这些大脑结构的变化可能是与儿科 TBI 相关的认知和行为缺陷的基础。或者,TBI 后脑回增多可能是一种代偿机制,尽管脑容量减少,但仍能使皮质表面积正常发育。