在患有生长激素缺乏症的儿童中,个体层面的形态相似性网络发生变化
Yanglei Cheng1, Liping Lin2, Weifeng Hou2
1Department of Endocrine, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Journal of neurodevelopmental disorders
|August 26, 2024
概括
儿科生长激素缺乏 (GHD) 显著改变大脑网络组织,影响运动和认知发育. 这项研究揭示了GHD儿童大脑连接的广泛变化.
科学领域:
- 神经科学是一个神经科学.
- 发展生物学 发展生物学
- 医疗成像医学成像
背景情况:
- 儿科生长激素缺乏症 (GHD) 与区域灰质 (GM) 变化有关.
- 在GHD中对大规模形态大脑网络 (MBNs) 的影响仍然在很大程度上未被描述.
研究的目的:
- 调查儿科GHD中个体级MBN的拓组织.
- 为了比较GHD患者和典型的发展对照 (TD) 之间的网络特性.
主要方法:
- 在61名GHD患者和42名TD中使用区域间的GM相似性构建了个人级别的MBNs.
- 分析了拓参数和基于网络的统计数据,以确定群体差异.
- 研究了网络属性与临床变量之间的关联.
主要成果:
- GHD患者表现出被破坏的小世界网络组织,在包括小脑,额头环和海马体在内的各种大脑区域的节点特性发生变化.
- 在传感运动,默认模式,视觉和听觉网络中观察到特定的网络干扰.
- 在GHD中改变的结节形状与血清标志物和行为评分相关.
结论:
- 儿科GHD涉及到大规模MBNs的广泛重组,可能是由于涉及皮质 - 状体 - thalamo - 小脑通路的异常电路.
- 在GHD中异常的形态连接性在运动,认知和语言功能的发育延迟中起着至关重要的作用.
- 这些发现强调了MBN分析对于理解GHD神经生物学基础的重要性.
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